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            type="text/xsl"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1111/(ISSN)1439-0264" xmlns="http://purl.org/rss/1.0/"><title>Anatomia, Histologia, Embryologia</title><description> Wiley Online Library : Anatomia, Histologia, Embryologia</description><link>http://dx.doi.org/10.1111%2F%28ISSN%291439-0264</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">Blackwell Verlag GmbH</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">0340-2096</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1439-0264</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">February 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">41</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">78</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/ahe.2012.41.issue-1/asset/cover.gif?v=1&amp;s=d6d39a0c11d5527b4e29d3d6679323124f09b026"/><items><rdf:Seq><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01137.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01136.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01133.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01130.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01135.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01123.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01134.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01132.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01131.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01127.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01129.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01128.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01125.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01126.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01124.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01122.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01119.x"/><rdf:li 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rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01105.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01096.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01097.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01099.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01098.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01100.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01101.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01102.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01104.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01103.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01109.x"/></rdf:Seq></items></channel><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01137.x" xmlns="http://purl.org/rss/1.0/"><title>Histochemical and Morphometric Analyses of the Musculature of the Forelimb of the Subterranean Rodent Ctenomys talarum (Octodontoidea)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01137.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Histochemical and Morphometric Analyses of the Musculature of the Forelimb of the Subterranean Rodent Ctenomys talarum (Octodontoidea)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. I. Alvarez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. O. Díaz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. V. Longo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Becerra</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. I. Vassallo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-06T14:27:17.700687-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2012.01137.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2012.01137.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01137.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Histochemical and morphometric analyses were performed to characterize the fibre-type composition of two forelimb muscles of the South American subterranean rodent <em>Ctenomys talarum</em>. The studied muscles were the triceps lateralis, an extensor of the elbow, and the teres major, a flexor of the shoulder. It was found that these muscles had an elevated proportion of fast oxidative-glycolytic (FOG) fibres, and lower proportions of slow oxidative (SO) and fast glycolytic (FG) fibres. This composition probably qualifies the teres major and triceps muscles to perform the sustained effort required in tunnelling excavation. The results were discussed considering published data on fibre-type composition of mammals having different modes of life and digging behaviour. We here suggest that <em>C. talarum</em> has the potential of generating forces linked to rapid, powerful movements during sustained periods by means of an elevated proportion of FOG fibres, together with osteological changes that result in a great mechanical advantage of the forelimb muscles.</p></div>]]></content:encoded><description>Histochemical and morphometric analyses were performed to characterize the fibre-type composition of two forelimb muscles of the South American subterranean rodent Ctenomys talarum. The studied muscles were the triceps lateralis, an extensor of the elbow, and the teres major, a flexor of the shoulder. It was found that these muscles had an elevated proportion of fast oxidative-glycolytic (FOG) fibres, and lower proportions of slow oxidative (SO) and fast glycolytic (FG) fibres. This composition probably qualifies the teres major and triceps muscles to perform the sustained effort required in tunnelling excavation. The results were discussed considering published data on fibre-type composition of mammals having different modes of life and digging behaviour. We here suggest that C. talarum has the potential of generating forces linked to rapid, powerful movements during sustained periods by means of an elevated proportion of FOG fibres, together with osteological changes that result in a great mechanical advantage of the forelimb muscles.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01136.x" xmlns="http://purl.org/rss/1.0/"><title>Embryonic and Fetal Development in – Pigmy Rice Rat – Oligoryzomys sp. (Rodentia, Sigmodontinae) and its Significance for Being a new Experimental Model</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01136.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Embryonic and Fetal Development in – Pigmy Rice Rat – Oligoryzomys sp. (Rodentia, Sigmodontinae) and its Significance for Being a new Experimental Model</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. O. Favaron</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. N. Rodrigues</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. F. Oliveira</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. M. Biasi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. A. Miglino</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-02T07:36:36.069707-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2012.01136.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2012.01136.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01136.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><em>Oligoryzomys</em> (Cricetidae, Sigmodontinae) is a common rodent genus from South America that includes a couple of very similar species. Related species have been used as experimental model for understanding several diseases for which these species are reservoirs. In order to provide a better understanding of the embryological aspects of this group, herein we showed data on the embryonic and fetal development in <em>Oligoryzomys</em> sp. Eight specimens of different stages of gestation were obtained from the Collection of the Zoology Museum of University of Sao Paulo, Brazil. Gestational ages were estimated by crown-rump-length according to Evans and Sack (<a href="#ahe1136-bib-0012" rel="references:#ahe1136-bib-0012"/>). To address our analysis after examining the gross morphology, tissues from several organs were processed for light and scanning electron microscopy. Morphological data on the systems (nervous system, cardiorespiratory system, intestinal tract and urogenital system) were described in detail. Finally, the findings were compared with what is known about embryological aspects in other rodent species in order to establish similarities and differences during the organogenesis in different species.</p></div>]]></content:encoded><description>Oligoryzomys (Cricetidae, Sigmodontinae) is a common rodent genus from South America that includes a couple of very similar species. Related species have been used as experimental model for understanding several diseases for which these species are reservoirs. In order to provide a better understanding of the embryological aspects of this group, herein we showed data on the embryonic and fetal development in Oligoryzomys sp. Eight specimens of different stages of gestation were obtained from the Collection of the Zoology Museum of University of Sao Paulo, Brazil. Gestational ages were estimated by crown-rump-length according to Evans and Sack (). To address our analysis after examining the gross morphology, tissues from several organs were processed for light and scanning electron microscopy. Morphological data on the systems (nervous system, cardiorespiratory system, intestinal tract and urogenital system) were described in detail. Finally, the findings were compared with what is known about embryological aspects in other rodent species in order to establish similarities and differences during the organogenesis in different species.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01133.x" xmlns="http://purl.org/rss/1.0/"><title>Use of a Culture Medium (McCoy®), as a Method for Evaluating Bos indicus × Bos taurus Embryos</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01133.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Use of a Culture Medium (McCoy®), as a Method for Evaluating Bos indicus × Bos taurus Embryos</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Godinez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. S. Galina</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Moreno-Mendoza</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Alarcon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. A. Lammoglia</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-20T05:29:46.960033-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01133.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01133.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01133.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The aim of this study was to use culture medium (McCoy®) as a test to evaluate the classification of embryos after a primary grading using stereoscopic microscopy to further confirm whether embryos have been correctly scored by stereoscopic microscopy evaluating the level of apoptosis. Forty-six <em>Bos indicus</em> embryos were collected with a non-surgical method and evaluated with stereoscopic microscopy for scoring in three categories (good, fair and poor). Cell proliferation and apoptosis were assessed and compared between the control group (<em>n</em> = 14) at the onset of the experiment and in an experimental group (<em>n</em> = 32) after stored for 4 h in a culture medium. Embryos were processed using TUNEL and BrdU markers to determine the apoptosis and cell proliferation. Seventy-four per cent of good quality embryos developed favourably after the 4 h of culture; 60% of fair embryos maintained their evolution, while 100% of poor quality embryos presented degenerative changes from the beginning. No statistical differences were found between the experimental and the control groups in the count of positive BrdU and apoptotic nuclei. In poor quality embryos, a higher number of apoptotic cells were found relative to good and fair embryos, both in the experimental and control groups (<em>P</em> &lt; 0.05). These results suggest that the culture medium may be used for a short time as a fast, practical and non-invasive alternative to further confirm whether embryos have been correctly scored by stereoscopic microscopy.</p></div>]]></content:encoded><description>The aim of this study was to use culture medium (McCoy®) as a test to evaluate the classification of embryos after a primary grading using stereoscopic microscopy to further confirm whether embryos have been correctly scored by stereoscopic microscopy evaluating the level of apoptosis. Forty-six Bos indicus embryos were collected with a non-surgical method and evaluated with stereoscopic microscopy for scoring in three categories (good, fair and poor). Cell proliferation and apoptosis were assessed and compared between the control group (n = 14) at the onset of the experiment and in an experimental group (n = 32) after stored for 4 h in a culture medium. Embryos were processed using TUNEL and BrdU markers to determine the apoptosis and cell proliferation. Seventy-four per cent of good quality embryos developed favourably after the 4 h of culture; 60% of fair embryos maintained their evolution, while 100% of poor quality embryos presented degenerative changes from the beginning. No statistical differences were found between the experimental and the control groups in the count of positive BrdU and apoptotic nuclei. In poor quality embryos, a higher number of apoptotic cells were found relative to good and fair embryos, both in the experimental and control groups (P &lt; 0.05). These results suggest that the culture medium may be used for a short time as a fast, practical and non-invasive alternative to further confirm whether embryos have been correctly scored by stereoscopic microscopy.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01130.x" xmlns="http://purl.org/rss/1.0/"><title>Polymelous Layer Chick Displaying Additional Malformations of the Hind Gut: Case Report and In-Depth Review of Related Literature</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01130.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Polymelous Layer Chick Displaying Additional Malformations of the Hind Gut: Case Report and In-Depth Review of Related Literature</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. M. Hirschberg</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Saleh</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Kaiser</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Lierz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. M. Hafez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. H. Bragulla</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-18T02:20:30.065231-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01130.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01130.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01130.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A case report of a male 6-day-old male layer chick featuring incomplete polymelia of the hind limbs and hindgut malformations is presented. The chick was submitted to computed tomography (CT) examination and subsequent anatomical dissection. Apart from the two supernumerary hind limbs, the anatomical dissection revealed additional hindgut alterations: three uniform-sized caeca flanked the ileum, and the rectum branched into paired cloacae. The supernumerary hind limbs were localized caudal to the normal hind limbs in an inverted position and were attached to pelvic girdle elements and to a curtate pygostyle. They featured a prominent unpaired femur besides paired tibiotarsi, tarsometatarsi and species-specific phalanges of the toes. Additionally, two separate bones attached to the caudoventral aspect of the regular hip bones were developed. The supernumerary limbs were in part mobile and received nerve and vascular supply. Digital 3D-reconstruction based on the CT datasets revealed the osseous components of the malformed body parts. The possible morphogenesis including an in-depth literature review and the clinical implications of the reported malformations are discussed.</p></div>]]></content:encoded><description>A case report of a male 6-day-old male layer chick featuring incomplete polymelia of the hind limbs and hindgut malformations is presented. The chick was submitted to computed tomography (CT) examination and subsequent anatomical dissection. Apart from the two supernumerary hind limbs, the anatomical dissection revealed additional hindgut alterations: three uniform-sized caeca flanked the ileum, and the rectum branched into paired cloacae. The supernumerary hind limbs were localized caudal to the normal hind limbs in an inverted position and were attached to pelvic girdle elements and to a curtate pygostyle. They featured a prominent unpaired femur besides paired tibiotarsi, tarsometatarsi and species-specific phalanges of the toes. Additionally, two separate bones attached to the caudoventral aspect of the regular hip bones were developed. The supernumerary limbs were in part mobile and received nerve and vascular supply. Digital 3D-reconstruction based on the CT datasets revealed the osseous components of the malformed body parts. The possible morphogenesis including an in-depth literature review and the clinical implications of the reported malformations are discussed.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01135.x" xmlns="http://purl.org/rss/1.0/"><title>Anatomical Architecture of the Brachial Plexus in the Common Hippopotamus (Hippopotamus amphibius) with Special Reference to the Derivation and Course of its Unique Branches</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01135.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Anatomical Architecture of the Brachial Plexus in the Common Hippopotamus (Hippopotamus amphibius) with Special Reference to the Derivation and Course of its Unique Branches</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Yoshitomi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Kawashima</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Murakami</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Takayanagi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Inoue</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Aoyagi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Sato</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-18T02:18:59.468509-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2012.01135.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2012.01135.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01135.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The anatomy of the brachial plexus in the common hippopotamus (<em>Hippopotamus amphibius</em>), which has not been previously reported, was first examined bilaterally in a newborn hippopotamus. Our observations clarified the following: (1) the brachial plexus comprises the fifth cervical (C5) to first thoracic (T1) nerves. These formed two trunks, C5–C6 and C7–T1; in addition, the axillary artery passed in between C6 and C7, (2) unique branches to the brachialis muscle and those of the lateral cutaneous antebrachii nerves ramified from the median nerve, (3) nerve fibre analysis revealed that these unique nerve branches from the median nerve were closely related and structurally similar to the musculocutaneous (MC) nerve; however, they had changed course from the MC to the median nerve, and (4) this unique branching pattern is likely to be a common morphological feature of the brachial plexus in amphibians, reptiles and certain mammals.</p></div>]]></content:encoded><description>The anatomy of the brachial plexus in the common hippopotamus (Hippopotamus amphibius), which has not been previously reported, was first examined bilaterally in a newborn hippopotamus. Our observations clarified the following: (1) the brachial plexus comprises the fifth cervical (C5) to first thoracic (T1) nerves. These formed two trunks, C5–C6 and C7–T1; in addition, the axillary artery passed in between C6 and C7, (2) unique branches to the brachialis muscle and those of the lateral cutaneous antebrachii nerves ramified from the median nerve, (3) nerve fibre analysis revealed that these unique nerve branches from the median nerve were closely related and structurally similar to the musculocutaneous (MC) nerve; however, they had changed course from the MC to the median nerve, and (4) this unique branching pattern is likely to be a common morphological feature of the brachial plexus in amphibians, reptiles and certain mammals.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01123.x" xmlns="http://purl.org/rss/1.0/"><title>Immunocytochemical Localization of Cytoplasmic and Nuclear Intermediate Filaments in the Bovine Ovary during Folliculogenesis</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01123.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Immunocytochemical Localization of Cytoplasmic and Nuclear Intermediate Filaments in the Bovine Ovary during Folliculogenesis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Wendl</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Ebach</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Rodler</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. A.-M. Kenngott</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-18T02:18:54.977838-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01123.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01123.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01123.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The cellular cytoskeleton is composed of three fibrillar systems, namely actin microfilaments, microtubules and intermediate filaments (IFs). It not only is a structural system, which mediates functional compartmentalization, but also contributes to many cellular processes such as transport, mitosis, secretion, formation of cell extensions, intercellular communication and apoptosis. In this study, we have examined the distribution of four groups of IFs [cytokeratins (CKs), vimentin, desmin and lamins] in the somatic and germinal cells of the bovine ovary using RT-PCR and immunohistochemical techniques. Using RT-PCR, specific transcripts for all intermediate proteins studied (CK8, CK18, desmin, vimentin, lamin A/C and lamin B1) were detected. A characteristic immunohistochemical staining pattern was observed for the different IFs within the ovary. In this study, we used antibodies against type I CK (acidic CKs: CK14, CK18 and CK19) and type II CK (basic CKs: CK5 and CK8). Among these, only antibodies against CK18 gave a characteristic pattern of immunostaining in the ovary, which included the surface epithelium, the follicle cells, the endothelium of blood vessels and rete ovarii. Antibodies against all other CKs resulted in a weak staining of a limited number of cellular structures (CK5 and CK19) or were completely negative (CK8 and CK14, apart from the surface epithelium). Vimentin antibodies resulted occasionally in a weak staining of the granulosa cells of primary and secondary follicles. In late secondary follicles, the basal and the most apical follicle cells contacting the zona pellucida usually showed a marked immunostaining for vimentin. In antral follicles, three different immunostaining patterns for vimentin were observed. Desmin immunostaining was confined to the smooth muscle cells of blood vessels. Although mRNA for lamin A/C and lamin B1 could be demonstrated using RT-PCR, no immunostaining was found for lamins, neither in the follicle cells nor in the oocytes.</p></div>]]></content:encoded><description>The cellular cytoskeleton is composed of three fibrillar systems, namely actin microfilaments, microtubules and intermediate filaments (IFs). It not only is a structural system, which mediates functional compartmentalization, but also contributes to many cellular processes such as transport, mitosis, secretion, formation of cell extensions, intercellular communication and apoptosis. In this study, we have examined the distribution of four groups of IFs [cytokeratins (CKs), vimentin, desmin and lamins] in the somatic and germinal cells of the bovine ovary using RT-PCR and immunohistochemical techniques. Using RT-PCR, specific transcripts for all intermediate proteins studied (CK8, CK18, desmin, vimentin, lamin A/C and lamin B1) were detected. A characteristic immunohistochemical staining pattern was observed for the different IFs within the ovary. In this study, we used antibodies against type I CK (acidic CKs: CK14, CK18 and CK19) and type II CK (basic CKs: CK5 and CK8). Among these, only antibodies against CK18 gave a characteristic pattern of immunostaining in the ovary, which included the surface epithelium, the follicle cells, the endothelium of blood vessels and rete ovarii. Antibodies against all other CKs resulted in a weak staining of a limited number of cellular structures (CK5 and CK19) or were completely negative (CK8 and CK14, apart from the surface epithelium). Vimentin antibodies resulted occasionally in a weak staining of the granulosa cells of primary and secondary follicles. In late secondary follicles, the basal and the most apical follicle cells contacting the zona pellucida usually showed a marked immunostaining for vimentin. In antral follicles, three different immunostaining patterns for vimentin were observed. Desmin immunostaining was confined to the smooth muscle cells of blood vessels. Although mRNA for lamin A/C and lamin B1 could be demonstrated using RT-PCR, no immunostaining was found for lamins, neither in the follicle cells nor in the oocytes.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01134.x" xmlns="http://purl.org/rss/1.0/"><title>BCL-2 Family of Proteins and Mammary Cellular Fate</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01134.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">BCL-2 Family of Proteins and Mammary Cellular Fate</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Colitti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-16T07:43:21.45089-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2012.01134.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2012.01134.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2012.01134.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This review focuses on the pro-apoptotic and anti-apoptotic Bcl-2 family members involved in apoptosis, which is the predominant process controlling cell remodelling during post-lactational mammary gland involution. The members of the Bcl-2 protein family, whose expression levels are under the control of lactogenic hormones, internally control this mechanism also during lactation. They can physically interact with each other, sometimes in an antagonistic manner. Mammary glands undergo repeated cycles of structural development, functional differentiation and regression, therefore provide a unique model for investigating this family of proteins that regulate the fate of the secretory cells and consequently milk yield. The involvement of Bcl-2 family members is reviewed in mammary tissue during morphogenesis, at different stages of lactation cycle and in comparison with dairy and laboratory animals.</p></div>]]></content:encoded><description>This review focuses on the pro-apoptotic and anti-apoptotic Bcl-2 family members involved in apoptosis, which is the predominant process controlling cell remodelling during post-lactational mammary gland involution. The members of the Bcl-2 protein family, whose expression levels are under the control of lactogenic hormones, internally control this mechanism also during lactation. They can physically interact with each other, sometimes in an antagonistic manner. Mammary glands undergo repeated cycles of structural development, functional differentiation and regression, therefore provide a unique model for investigating this family of proteins that regulate the fate of the secretory cells and consequently milk yield. The involvement of Bcl-2 family members is reviewed in mammary tissue during morphogenesis, at different stages of lactation cycle and in comparison with dairy and laboratory animals.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01132.x" xmlns="http://purl.org/rss/1.0/"><title>Identification of Gonadal Tissue in Cryptorchid Stallion can be Improved by Molecular Biological Analysis – A Case Report</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01132.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Identification of Gonadal Tissue in Cryptorchid Stallion can be Improved by Molecular Biological Analysis – A Case Report</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Stumpf</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Fietz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Ezer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L.-F. Litzke</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Bergmann</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-16T07:42:08.743428-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01132.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01132.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01132.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Short Communication</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Surgically removed testicular tissue in cryptorchid stallions is sometimes difficult to identify because of morphological and histological malformation. Therefore, a sure method to characterise the removed tissue is required. A 2-year-old Haflinger stallion was castrated after diagnosis of cryptorchidism to remove the left intra-abdomnial testis. Intra-operative exploration of the abdominal cavity revealed a firm, dysmorphic structure, which could not be identified as testis based on macroscopic anatomy. The removed tissue was Bouin-fixed and paraffin-embedded for histological examination. We additionally applied immuno-histochemistry for smooth muscle actin to identify tubular structures as well as reverse transcriptase polymerase chain reaction (RT-PCR) to detect the expression of steroidogenic acute regulatory protein (StAR), indicating the presence of Leydig cells. A hCG test was conducted after surgery to screen for remaining testicular tissue. Histological examination using haematoxylin and eosin staining revealed signs of tissue calcification, amorph matrix with scattered cells and round structures. The latter could not be definitely identified as tubules. Actin staining revealed a few tubular wall structures. StAR mRNA expression indicated the presence of Leydig cells in parts of the removed tissue. The hCG test after castration showed no increase in testosterone. Histological and molecular biological examination of extirpated tissue in cryptorchid stallions can play an important role in the identification of the malformed testes like structures. The use of molecular biological techniques provides the opportunity to characterise surgically removed abdominal tissue that cannot be clearly diagnosed by routine histological examination.</p></div>]]></content:encoded><description>Surgically removed testicular tissue in cryptorchid stallions is sometimes difficult to identify because of morphological and histological malformation. Therefore, a sure method to characterise the removed tissue is required. A 2-year-old Haflinger stallion was castrated after diagnosis of cryptorchidism to remove the left intra-abdomnial testis. Intra-operative exploration of the abdominal cavity revealed a firm, dysmorphic structure, which could not be identified as testis based on macroscopic anatomy. The removed tissue was Bouin-fixed and paraffin-embedded for histological examination. We additionally applied immuno-histochemistry for smooth muscle actin to identify tubular structures as well as reverse transcriptase polymerase chain reaction (RT-PCR) to detect the expression of steroidogenic acute regulatory protein (StAR), indicating the presence of Leydig cells. A hCG test was conducted after surgery to screen for remaining testicular tissue. Histological examination using haematoxylin and eosin staining revealed signs of tissue calcification, amorph matrix with scattered cells and round structures. The latter could not be definitely identified as tubules. Actin staining revealed a few tubular wall structures. StAR mRNA expression indicated the presence of Leydig cells in parts of the removed tissue. The hCG test after castration showed no increase in testosterone. Histological and molecular biological examination of extirpated tissue in cryptorchid stallions can play an important role in the identification of the malformed testes like structures. The use of molecular biological techniques provides the opportunity to characterise surgically removed abdominal tissue that cannot be clearly diagnosed by routine histological examination.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01131.x" xmlns="http://purl.org/rss/1.0/"><title>Retrograde Tracing with Fluorescent Microspheres Reveals Bifurcating Projections from Central Retina to Tectum and Thalamus in Chicks</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01131.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Retrograde Tracing with Fluorescent Microspheres Reveals Bifurcating Projections from Central Retina to Tectum and Thalamus in Chicks</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Cao</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Naito</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Chen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-16T07:42:02.296573-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01131.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01131.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01131.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Short Communication</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The goal of this study is to demonstrate the dual-projection pattern of retinal ganglion cells (RGCs) projecting to the tectum and visual thalamus in chick using retrograde fluorescent tracers and also to define the morphological properties of these RGCs with dual projections by intracellular injection of Lucifer Yellow (LY) combined with immunohistochemistry. Thirty-two chicks received double injections of green and red fluorescent microspheres into their thalamus and tectum in the same side. In the central retina, most of the labelled RGCs were tec-RGCs (RGCs projecting to the tectum), a quarter was tha-RGCs (RGCs projecting to the thalamus), and almost all of the tha-RGCs were double-labelled RGCs. An intracellular injection of LY into the double-labelled RGCs showed all six groups of RGCs without specific populations in each group (J. Comp. Neurol., 2004, 469: 360). These dendritic patterns were mostly mono- and bistrata, which extended horizontally in the deeper part of the inner plexiform layer.</p></div>]]></content:encoded><description>The goal of this study is to demonstrate the dual-projection pattern of retinal ganglion cells (RGCs) projecting to the tectum and visual thalamus in chick using retrograde fluorescent tracers and also to define the morphological properties of these RGCs with dual projections by intracellular injection of Lucifer Yellow (LY) combined with immunohistochemistry. Thirty-two chicks received double injections of green and red fluorescent microspheres into their thalamus and tectum in the same side. In the central retina, most of the labelled RGCs were tec-RGCs (RGCs projecting to the tectum), a quarter was tha-RGCs (RGCs projecting to the thalamus), and almost all of the tha-RGCs were double-labelled RGCs. An intracellular injection of LY into the double-labelled RGCs showed all six groups of RGCs without specific populations in each group (J. Comp. Neurol., 2004, 469: 360). These dendritic patterns were mostly mono- and bistrata, which extended horizontally in the deeper part of the inner plexiform layer.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01127.x" xmlns="http://purl.org/rss/1.0/"><title>Development of Purkinje Cells in the Ovine Brain</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01127.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Development of Purkinje Cells in the Ovine Brain</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Salouci</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">V. Engelen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Gyan</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Antoine</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Jacqmot</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Mignon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Kirschvink</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Gabriel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-06T03:54:08.00571-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01127.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01127.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01127.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Purkinje cells are involved in many vital functions within the body. Twenty ovine fetuses ranging from 2 to 5 months of gestation, two lambs in the first week after birth and three adult sheep were studied. Sections of the cerebellum were stained with haematoxylin and eosin, cresyl violet and Klüver–Barrera. This study indicates that Purkinje cells began to appear after the 15<sup>th</sup> week of gestation. There were varying degrees of development of Purkinje cells in different zones of the cerebellum. Our findings in sheep fetuses suggest that the maturation of Purkinje cells starts in the caudal regions of the cerebellum and that the process begins in the vermis before it does in the cerebellar hemispheres. The alignment of Purkinje cells was found to be very regular in the caudal regions of the cerebellum. A partial absence of Purkinje cells in the rostral regions of the cerebellum was observed in both sheep fetuses and adult sheep. In the first post-natal week, some ectopic Purkinje cells were found in the white matter of the cerebellum.</p></div>]]></content:encoded><description>Purkinje cells are involved in many vital functions within the body. Twenty ovine fetuses ranging from 2 to 5 months of gestation, two lambs in the first week after birth and three adult sheep were studied. Sections of the cerebellum were stained with haematoxylin and eosin, cresyl violet and Klüver–Barrera. This study indicates that Purkinje cells began to appear after the 15th week of gestation. There were varying degrees of development of Purkinje cells in different zones of the cerebellum. Our findings in sheep fetuses suggest that the maturation of Purkinje cells starts in the caudal regions of the cerebellum and that the process begins in the vermis before it does in the cerebellar hemispheres. The alignment of Purkinje cells was found to be very regular in the caudal regions of the cerebellum. A partial absence of Purkinje cells in the rostral regions of the cerebellum was observed in both sheep fetuses and adult sheep. In the first post-natal week, some ectopic Purkinje cells were found in the white matter of the cerebellum.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01129.x" xmlns="http://purl.org/rss/1.0/"><title>Abdominal Exploration in Captive Collared Peccaries (Tayassu tajacu) by Ultrasonography</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01129.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Abdominal Exploration in Captive Collared Peccaries (Tayassu tajacu) by Ultrasonography</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. C. X. Peixoto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. R. S. Oliveira</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. D. Alves</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. F. Oliveira</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. R. Silva</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-06T03:51:52.157489-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01129.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01129.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01129.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study determines the morphology and ultrasound features of the abdominal organs in male, nestling and healthy collared peccaries. The bladder wall is hyperechogenic, with a thickness of 0.2 ± 0.08 cm. The kidneys present a well-defined cortex, medulla and pelvis, and the dimensions are 2.56 ± 0.3 × 4.6 ± 0.8 cm for the left and 2.51 ± 0.4 × 4.86 ± 1.1 cm for the right kidney. The spleen has a uniform echotexture over its entire surface. The largest dimensions of the liver are 2.0 ± 0.57 cm for the left lobe and 1.42 ± 0.66 cm for the caudate lobe. The liver presents a homogeneous echotexture in the majority of cases, but sometimes some hyperechoic spots are present. The stomach wall has a thickness of 0.42 ± 0.28 cm. The bowel loops show alternate hyperechoic and hypoechoic layers with a uniform diameter and a wall thickness of 0.19 ± 0.07 cm.</p></div>]]></content:encoded><description>This study determines the morphology and ultrasound features of the abdominal organs in male, nestling and healthy collared peccaries. The bladder wall is hyperechogenic, with a thickness of 0.2 ± 0.08 cm. The kidneys present a well-defined cortex, medulla and pelvis, and the dimensions are 2.56 ± 0.3 × 4.6 ± 0.8 cm for the left and 2.51 ± 0.4 × 4.86 ± 1.1 cm for the right kidney. The spleen has a uniform echotexture over its entire surface. The largest dimensions of the liver are 2.0 ± 0.57 cm for the left lobe and 1.42 ± 0.66 cm for the caudate lobe. The liver presents a homogeneous echotexture in the majority of cases, but sometimes some hyperechoic spots are present. The stomach wall has a thickness of 0.42 ± 0.28 cm. The bowel loops show alternate hyperechoic and hypoechoic layers with a uniform diameter and a wall thickness of 0.19 ± 0.07 cm.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01128.x" xmlns="http://purl.org/rss/1.0/"><title>Morphofunctional Evaluation of the Testicle and the Spermatogenic Process of Adult White-Eyed Parakeets (Aratinga leucophthalma MULLER, 1776) During the Different Seasons of the Year</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01128.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphofunctional Evaluation of the Testicle and the Spermatogenic Process of Adult White-Eyed Parakeets (Aratinga leucophthalma MULLER, 1776) During the Different Seasons of the Year</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. V. Peixoto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. A. R. Paula</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. K. Balarini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. L. P. Matta</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. A. D. Santos</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. B. Lima</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. V. Peixoto</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-03T00:45:58.320541-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01128.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01128.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01128.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this experiment, testicle fragments of 14 adult White-eyed Parakeets (<em>Aratinga leucophthalma</em>) were evaluated as for their seasonal reproductive activities using the following quantitative parameters: average thickness of the testicular tunica albuginea, volumetric proportion of tubular and extratubular compartments, average diameter of the seminiferous tubules and corporal weight. Parameters were created for qualitative evaluations of the degree of spermatogenic development. In this experiment, all the animals were distributed into four groups, and their testicular fragments were collected during the middle of summer, fall, winter and spring. The animals were submitted to volatile general anaesthesia, and a biopsy was made by celioscopy. The fragments collected were processed histologically. The slides were prepared and later evaluated by using an optical microscope. The average seasonal values of the corporal weight increased, starting in the winter and reaching the peak during the spring. A seasonal testicle cycle was observed, because, in the spring, the testicles showed values for the quantitative and qualitative parameters of spermatic production compatible with the period of greater activity, while the opposite thing happened during the fall. Our data indicate that the parameters of sperm production may be correlated with daily light rather than with air humidity.</p></div>]]></content:encoded><description>In this experiment, testicle fragments of 14 adult White-eyed Parakeets (Aratinga leucophthalma) were evaluated as for their seasonal reproductive activities using the following quantitative parameters: average thickness of the testicular tunica albuginea, volumetric proportion of tubular and extratubular compartments, average diameter of the seminiferous tubules and corporal weight. Parameters were created for qualitative evaluations of the degree of spermatogenic development. In this experiment, all the animals were distributed into four groups, and their testicular fragments were collected during the middle of summer, fall, winter and spring. The animals were submitted to volatile general anaesthesia, and a biopsy was made by celioscopy. The fragments collected were processed histologically. The slides were prepared and later evaluated by using an optical microscope. The average seasonal values of the corporal weight increased, starting in the winter and reaching the peak during the spring. A seasonal testicle cycle was observed, because, in the spring, the testicles showed values for the quantitative and qualitative parameters of spermatic production compatible with the period of greater activity, while the opposite thing happened during the fall. Our data indicate that the parameters of sperm production may be correlated with daily light rather than with air humidity.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01125.x" xmlns="http://purl.org/rss/1.0/"><title>Fish Gills Alterations as Potential Biomarkers of Environmental Quality in a Eutrophized Tropical River in South-Eastern Brazil</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01125.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fish Gills Alterations as Potential Biomarkers of Environmental Quality in a Eutrophized Tropical River in South-Eastern Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. A. Nascimento</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. G. Araújo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. D. Gomes</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. M. M. Mendes</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Sales</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-03T00:44:49.632703-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01125.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01125.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01125.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Gill anomalies in three common fish species of different taxonomic order, habitat dwelling and feeding habits (one Characiformes, <em>Oligosarcus hepsetus</em>; one Siluriformes, <em>Hypostomus auroguttatus</em>; and one Perciformes, <em>Geophagus brasiliensis</em>) from a eutrophized tropical river in south-eastern in Brazil were compared. The aim of this study was to search for sentinel species that could be used as potential biomarkers of environmental quality. Most fish had gills with histological changes, namely epithelial lifting, interstitial oedema, leucocyte infiltration, hyperplasia of the epithelial cells, lamellar fusion, vasodilatation and necrosis. On the other hand, lamellar blood congestion and lamellar aneurysm, which are more serious and often irreversible changes, were recorded for the water column carnivorous <em>O. hepsetus</em> and, to a lesser extent, for the bottom-dwelling detritivorous <em>H. auroguttatus</em>. A histopathological alteration index (HAI) based on the occurrence and severity of gills anomalies indicated that <em>O. hepsetus</em> (mean score = 11.4) had significantly higher values (Kruskall–Wallis <em>H</em><sub>2,41</sub> = 15.95, <em>P</em> = 0.0003) compared with <em>G. brasiliensis</em> (mean score = 7.0). Overall, the omnivorous <em>G. brasiliensis</em> had comparatively lesser occurrence of most gill anomalies compared with other two species, being less suitable as biomarker of environmental quality. In contrast, the water column–dweller <em>O. hepsetus</em> (water column) and the bottom-dweller <em>H. auroguttatus</em> had gills most susceptible to changes, making them more suitable for using as histological biomarkers of the environmental quality in entrophized tropical rivers.</p></div>]]></content:encoded><description>Gill anomalies in three common fish species of different taxonomic order, habitat dwelling and feeding habits (one Characiformes, Oligosarcus hepsetus; one Siluriformes, Hypostomus auroguttatus; and one Perciformes, Geophagus brasiliensis) from a eutrophized tropical river in south-eastern in Brazil were compared. The aim of this study was to search for sentinel species that could be used as potential biomarkers of environmental quality. Most fish had gills with histological changes, namely epithelial lifting, interstitial oedema, leucocyte infiltration, hyperplasia of the epithelial cells, lamellar fusion, vasodilatation and necrosis. On the other hand, lamellar blood congestion and lamellar aneurysm, which are more serious and often irreversible changes, were recorded for the water column carnivorous O. hepsetus and, to a lesser extent, for the bottom-dwelling detritivorous H. auroguttatus. A histopathological alteration index (HAI) based on the occurrence and severity of gills anomalies indicated that O. hepsetus (mean score = 11.4) had significantly higher values (Kruskall–Wallis H2,41 = 15.95, P = 0.0003) compared with G. brasiliensis (mean score = 7.0). Overall, the omnivorous G. brasiliensis had comparatively lesser occurrence of most gill anomalies compared with other two species, being less suitable as biomarker of environmental quality. In contrast, the water column–dweller O. hepsetus (water column) and the bottom-dweller H. auroguttatus had gills most susceptible to changes, making them more suitable for using as histological biomarkers of the environmental quality in entrophized tropical rivers.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01126.x" xmlns="http://purl.org/rss/1.0/"><title>Growth and Shape Modelling of the Rabbit Tibia</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01126.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Growth and Shape Modelling of the Rabbit Tibia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">U. E. Pazzaglia</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Zarattini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Spagnuolo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Superti</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Marchese</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-03T00:44:45.971984-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01126.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01126.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01126.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The proliferative impulse of the growth plate cartilage and related structures and its effect on the dimensions of long bones are well documented. The modulation of shape, however, is less known, and in general, it is referred to the coupled resorption/apposition process of bone modelling. A morphometric study was carried out on rabbit tibiae comparing size increments and shape changes in relation to age. Utilizing measurements made using dried bones, radiography and computerized tomography, it was possible to perform a three-dimensional analysis of shape modulation occurring during a period of growth extending from 3 months to 1 year of age. The dynamics of the shape changes related to growth were studied with a fluorescent tetracycline labelling. This enabled correlation of shape modulation with the 3-D distribution of apposition and resorption. The current thinking behind the influences and mechanical forces affecting bone architecture was discussed in the light of these findings. Several factors play a role in the structural organization of the human and upper vertebrates’ skeleton, whose shape is genetically determined in the complex process usually referred as ‘modelling’. This does not conflict with the existing evidence of remodelling being influenced by mechanical stimuli, but the unsolved question remains how physical forces (strains) act on the biological substrate of cartilage and bone cells.</p></div>]]></content:encoded><description>The proliferative impulse of the growth plate cartilage and related structures and its effect on the dimensions of long bones are well documented. The modulation of shape, however, is less known, and in general, it is referred to the coupled resorption/apposition process of bone modelling. A morphometric study was carried out on rabbit tibiae comparing size increments and shape changes in relation to age. Utilizing measurements made using dried bones, radiography and computerized tomography, it was possible to perform a three-dimensional analysis of shape modulation occurring during a period of growth extending from 3 months to 1 year of age. The dynamics of the shape changes related to growth were studied with a fluorescent tetracycline labelling. This enabled correlation of shape modulation with the 3-D distribution of apposition and resorption. The current thinking behind the influences and mechanical forces affecting bone architecture was discussed in the light of these findings. Several factors play a role in the structural organization of the human and upper vertebrates’ skeleton, whose shape is genetically determined in the complex process usually referred as ‘modelling’. This does not conflict with the existing evidence of remodelling being influenced by mechanical stimuli, but the unsolved question remains how physical forces (strains) act on the biological substrate of cartilage and bone cells.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01124.x" xmlns="http://purl.org/rss/1.0/"><title>Ultrastructure of the Spermatozoa of the Domestic Duck (Anas platyrhynchos sp.)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01124.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ultrastructure of the Spermatozoa of the Domestic Duck (Anas platyrhynchos sp.)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Simões</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. M. Orsi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. M. B. Artoni</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-03T00:44:38.03926-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01124.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01124.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01124.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The ultrastructure of the spermatozoa of the domestic duck (<em>Anas platyrhynchos</em> sp.) was analysed by transmission and scanning electron microscopies and compared with the results obtained in preliminary studies involving other non-passerine birds. The spermatozoa were characterised by the presence of a short head, short midpiece and long principal piece. The head consisted of a reduced acrosome that contained moderately electron-dense homogenous material. The implantation fossa was observed between the base of the nucleus and the proximal centriole. The midpiece contained electron-dense material associated with the proximal centriole and nuclear membrane, and a long distal centriole surrounded throughout its length by 11–12 elliptical mitochondria. A dense annulus separating the midpiece from the principal piece was visible. Posterior to the annulus, the axoneme was formed surrounded by a dense fibrous sheath, representing the principal piece or flagellum, which was a long segment with a smooth surface and a smaller diameter than the midpiece. The spermatozoon of the domestic duck resembles that of other non-passerine birds, corresponding to a basic type of spermatozoon similar to that of reptiles, called sauropsid type.</p></div>]]></content:encoded><description>The ultrastructure of the spermatozoa of the domestic duck (Anas platyrhynchos sp.) was analysed by transmission and scanning electron microscopies and compared with the results obtained in preliminary studies involving other non-passerine birds. The spermatozoa were characterised by the presence of a short head, short midpiece and long principal piece. The head consisted of a reduced acrosome that contained moderately electron-dense homogenous material. The implantation fossa was observed between the base of the nucleus and the proximal centriole. The midpiece contained electron-dense material associated with the proximal centriole and nuclear membrane, and a long distal centriole surrounded throughout its length by 11–12 elliptical mitochondria. A dense annulus separating the midpiece from the principal piece was visible. Posterior to the annulus, the axoneme was formed surrounded by a dense fibrous sheath, representing the principal piece or flagellum, which was a long segment with a smooth surface and a smaller diameter than the midpiece. The spermatozoon of the domestic duck resembles that of other non-passerine birds, corresponding to a basic type of spermatozoon similar to that of reptiles, called sauropsid type.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01122.x" xmlns="http://purl.org/rss/1.0/"><title>Neurochemical Properties of Aquaporin 1-Expressing Sensory Neurons from the Ovine Trigeminal Ganglion</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01122.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Neurochemical Properties of Aquaporin 1-Expressing Sensory Neurons from the Ovine Trigeminal Ganglion</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. B. Arciszewski</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-12T23:25:15.003933-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01122.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01122.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01122.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Aims of the present study were to investigate the distribution and morphology of aquaporin 1-immunoreactive (AQP1-IR) neurons in the sensory ganglia of the sheep. Double immunohistochemical staining was applied to figure out whether substance P (SP), calcitonin gene-related peptide (CGRP) and galanin are present in AQP1-bearing primary afferent neurons. The expression of AQP1 was present only in trigeminal ganglion, whereas in nodose ganglion, jugular ganglion as well as C<sub>1</sub>–C<sub>7</sub> dorsal root ganglia no presence of AQP1 was found. In trigeminal ganglion, 15.4 ± 2.3% of Hu C/D-IR neurons (pan-neuronal marker) showed the presence of AQP1. The vast majority of AQP1-IR trigeminal sensory neurons (approximately 69.6 ± 3.3%, <em>n</em> = 5) were classified as middle in size, 28.6 ± 3.0% of AQP1-IR neurons were small and only 1.8 ± 0.6% of AQP1-positive neurons were large in size. Amongst the population of AQP1-IR trigeminal neurons as many as 58.5 ± 3.9% were immunopositive to SP, 30.7 ± 2.3% showed the presence of CGRP and 10.9 ± 0.2% coexpressed galanin. In trigeminal ganglion, SP-IR as well as CGRP-IR (but not galanin-IR) nerve fibres were found in close neighbourhood of AQP1-IR neurons. It is concluded that AQP1 is present in certain neuronal subsets of the ovine trigeminal ganglion; however, the exact role of this water channel has to be elucidated.</p></div>]]></content:encoded><description>Aims of the present study were to investigate the distribution and morphology of aquaporin 1-immunoreactive (AQP1-IR) neurons in the sensory ganglia of the sheep. Double immunohistochemical staining was applied to figure out whether substance P (SP), calcitonin gene-related peptide (CGRP) and galanin are present in AQP1-bearing primary afferent neurons. The expression of AQP1 was present only in trigeminal ganglion, whereas in nodose ganglion, jugular ganglion as well as C1–C7 dorsal root ganglia no presence of AQP1 was found. In trigeminal ganglion, 15.4 ± 2.3% of Hu C/D-IR neurons (pan-neuronal marker) showed the presence of AQP1. The vast majority of AQP1-IR trigeminal sensory neurons (approximately 69.6 ± 3.3%, n = 5) were classified as middle in size, 28.6 ± 3.0% of AQP1-IR neurons were small and only 1.8 ± 0.6% of AQP1-positive neurons were large in size. Amongst the population of AQP1-IR trigeminal neurons as many as 58.5 ± 3.9% were immunopositive to SP, 30.7 ± 2.3% showed the presence of CGRP and 10.9 ± 0.2% coexpressed galanin. In trigeminal ganglion, SP-IR as well as CGRP-IR (but not galanin-IR) nerve fibres were found in close neighbourhood of AQP1-IR neurons. It is concluded that AQP1 is present in certain neuronal subsets of the ovine trigeminal ganglion; however, the exact role of this water channel has to be elucidated.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01119.x" xmlns="http://purl.org/rss/1.0/"><title>Preliminary Study on the Mineral Apposition Rate in distal femoral epiphysis of New Zealand White Rabbit at Skeletal Maturity</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01119.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Preliminary Study on the Mineral Apposition Rate in distal femoral epiphysis of New Zealand White Rabbit at Skeletal Maturity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Cacchioli</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Ravanetti</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L. Soliani</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Borghetti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-08T05:34:09.214579-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01119.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01119.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01119.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 3 figures and 1 table</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Studies investigating the effect of different factors on the skeletal system require characterization of an appropriate animal model. Rabbits are among the most commonly studied animals for medical research, being used in about 35% of musculoskeletal research studies. The present dynamic cross-sectional histomorphometric study quantitatively determined mineral apposition rates (MARs) in the distal femoral epiphysis in four regions of interest (ROIs) in New Zealand white rabbits. ROIs included the craniolateral (CrL), caudolateral (CaL), craniomedial (CrM) and caudomedial (CaM) areas, using a reference height at different stages of skeletal maturity corresponding to experimental ages of 6, 7 and 8 months old (M6, M7 and M8). We evaluated whether a correlation exists in MARs between the times and the regions examined. Such data could be used in studies on growth of the rabbit’s femur, on biomaterials for bone integration or regeneration and on growth disturbances produced by various pathologic factors. We found no interaction at the experimental times; thus, M6, M7 and M8 are considered homogeneous in terms of MARs. The velocity profiles of the MARs were statistically significantly different among the considered ROIs. For all experimental times, the CrM region had a higher MAR than the other ROIs. Both the CrM and CaM ROIs had higher MARs than the corresponding lateral ROIs. Our results indicate that bone formation is not constant within the cross-section, but is statistically different between the ROIs considered.</p></div></div>]]></content:encoded><description>With 3 figures and 1 tableSummaryStudies investigating the effect of different factors on the skeletal system require characterization of an appropriate animal model. Rabbits are among the most commonly studied animals for medical research, being used in about 35% of musculoskeletal research studies. The present dynamic cross-sectional histomorphometric study quantitatively determined mineral apposition rates (MARs) in the distal femoral epiphysis in four regions of interest (ROIs) in New Zealand white rabbits. ROIs included the craniolateral (CrL), caudolateral (CaL), craniomedial (CrM) and caudomedial (CaM) areas, using a reference height at different stages of skeletal maturity corresponding to experimental ages of 6, 7 and 8 months old (M6, M7 and M8). We evaluated whether a correlation exists in MARs between the times and the regions examined. Such data could be used in studies on growth of the rabbit’s femur, on biomaterials for bone integration or regeneration and on growth disturbances produced by various pathologic factors. We found no interaction at the experimental times; thus, M6, M7 and M8 are considered homogeneous in terms of MARs. The velocity profiles of the MARs were statistically significantly different among the considered ROIs. For all experimental times, the CrM region had a higher MAR than the other ROIs. Both the CrM and CaM ROIs had higher MARs than the corresponding lateral ROIs. Our results indicate that bone formation is not constant within the cross-section, but is statistically different between the ROIs considered.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01121.x" xmlns="http://purl.org/rss/1.0/"><title>Eggs Ultrastructure and Early Development of Franciscodoras marmoratus (Pisces: Doradidae)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01121.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Eggs Ultrastructure and Early Development of Franciscodoras marmoratus (Pisces: Doradidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Alberto Weber</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Sato</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Enemir Santos</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Rizzo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Bazzoli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-08T05:31:51.701084-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01121.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01121.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01121.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Summary</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study presents, for the first time, information on the eggs and early development of <em>Franciscodoras marmoratus</em>, fish of São Francisco river, Brazil. To analyse the egg ultrastructure and morphological events of embryogenesis, a total of 36 <em>F. marmoratus</em> specimens (18 males and 18 females) were captured and subjected to spawning induction. Gametes were collected by manual extrusion, and fertilization was conducted using the dry method. After fertilization, eggs were kept in incubators with water temperature of 24°C. The embryonic development was monitored using a stereomicroscope until hatching. There was a 67% positive response to hypophysation by the females and the fertilization rate was 73.8 ± 6.2%. The oocytes are discoid, yellow, adhesive and covered by a thick jelly coat. Under the electron scanning microscope, the oocytes presented a surface with pore canals and funnel-shaped micropyle with a smooth vestibule. Recently extruded oocytes had a mean diameter of 1.27 ± 0.4 mm and after hydration was 1.91 ± 0.05 mm. The jelly coat was 0.34 ± 0.03 mm thickness, and the perivitelline space was 0.19 ± 0.04 mm. Eight phases of the embryonic development were identified, and embryogenesis was completed at 47 h after fertilization, at 24°C water temperature. The recently hatched larvae had 2.76 ± 0.57 mm of total length. These results provide useful information for the successful breeding and reproductive strategies of fishes.</p></div>]]></content:encoded><description>This study presents, for the first time, information on the eggs and early development of Franciscodoras marmoratus, fish of São Francisco river, Brazil. To analyse the egg ultrastructure and morphological events of embryogenesis, a total of 36 F. marmoratus specimens (18 males and 18 females) were captured and subjected to spawning induction. Gametes were collected by manual extrusion, and fertilization was conducted using the dry method. After fertilization, eggs were kept in incubators with water temperature of 24°C. The embryonic development was monitored using a stereomicroscope until hatching. There was a 67% positive response to hypophysation by the females and the fertilization rate was 73.8 ± 6.2%. The oocytes are discoid, yellow, adhesive and covered by a thick jelly coat. Under the electron scanning microscope, the oocytes presented a surface with pore canals and funnel-shaped micropyle with a smooth vestibule. Recently extruded oocytes had a mean diameter of 1.27 ± 0.4 mm and after hydration was 1.91 ± 0.05 mm. The jelly coat was 0.34 ± 0.03 mm thickness, and the perivitelline space was 0.19 ± 0.04 mm. Eight phases of the embryonic development were identified, and embryogenesis was completed at 47 h after fertilization, at 24°C water temperature. The recently hatched larvae had 2.76 ± 0.57 mm of total length. These results provide useful information for the successful breeding and reproductive strategies of fishes.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01120.x" xmlns="http://purl.org/rss/1.0/"><title>Effect of Oestradiol on Mast Cell Number and Histamine Level in the Mammary Glands of Rat</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01120.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of Oestradiol on Mast Cell Number and Histamine Level in the Mammary Glands of Rat</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Jing</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Z. Wang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Chen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-24T01:46:15.44538-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01120.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01120.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01120.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 3 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Variations of mast cell number, histamine concentration and oestrogen receptor (ER) expression in mammary glands with the fluctuation of plasma oestradiol level were identified either in the intact rats at different oestrous stages or in the ovary-ectomized rats administrated with different doses of oestradiol benzoate. The results showed that the number of mast cells and histamine concentration fluctuated concomitantly with plasma oestradiol level during the oestrous cycle. More mast cell number and higher histamine concentrations were observed in the oestrous stage than that in the prooestrous and dioestrous stages. Ovariectomy decreased the mast cell number and histamine concentration, which were reconstituted by exogenous oestradiol. ER was mainly found in the nuclear of epithelial cells and interstitial cells of mammary glands. In addition, ER was also expressed in the cytoplasm of some stromal cells. These stromal cells were verified to be mast cells. In conclusion, our results suggested that oestradiol modulated mast cell number and its degranulation in the mammary gland through the ERs pathway.</p></div></div>]]></content:encoded><description>With 3 figuresSummaryVariations of mast cell number, histamine concentration and oestrogen receptor (ER) expression in mammary glands with the fluctuation of plasma oestradiol level were identified either in the intact rats at different oestrous stages or in the ovary-ectomized rats administrated with different doses of oestradiol benzoate. The results showed that the number of mast cells and histamine concentration fluctuated concomitantly with plasma oestradiol level during the oestrous cycle. More mast cell number and higher histamine concentrations were observed in the oestrous stage than that in the prooestrous and dioestrous stages. Ovariectomy decreased the mast cell number and histamine concentration, which were reconstituted by exogenous oestradiol. ER was mainly found in the nuclear of epithelial cells and interstitial cells of mammary glands. In addition, ER was also expressed in the cytoplasm of some stromal cells. These stromal cells were verified to be mast cells. In conclusion, our results suggested that oestradiol modulated mast cell number and its degranulation in the mammary gland through the ERs pathway.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01118.x" xmlns="http://purl.org/rss/1.0/"><title>Thoraco-Omphalopagus Conjoined Twins in Chamois-Coloured Domestic Goat Kids</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01118.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Thoraco-Omphalopagus Conjoined Twins in Chamois-Coloured Domestic Goat Kids</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Binanti</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Riccaboni</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-10T04:38:53.102206-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01118.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01118.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01118.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 2 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Conjoined twins have been observed in a wide range of mammalian and non-mammalian species; they are considered to be more common in bovine, less frequent in sheep and pig and extremely rare in horse and goat. A pair of female conjoined twins was delivered from a 2-year-old Chamois-coloured domestic goat. Post-mortem examination revealed two identical and symmetrical twins, fused from the manubrium sterni to the region just caudal to the umbilicus. The rib cages were conjoined in the ventral plane with a single set of pericardial, pleural and peritoneal cavities. Internal examination revealed the presence of a common diaphragm and a single enlarged liver. Within a single central pericardium, two malformed hearts were present. Reports on this type of congenital duplication in goats have not been found in the literature. Thoracopagus and thoraco-omphalopagus are the most common types of conjoined twins in human beings and are associated with the highest mortality because of the frequent incidence of complex cardiac anatomy.</p></div></div>]]></content:encoded><description>With 2 figuresSummaryConjoined twins have been observed in a wide range of mammalian and non-mammalian species; they are considered to be more common in bovine, less frequent in sheep and pig and extremely rare in horse and goat. A pair of female conjoined twins was delivered from a 2-year-old Chamois-coloured domestic goat. Post-mortem examination revealed two identical and symmetrical twins, fused from the manubrium sterni to the region just caudal to the umbilicus. The rib cages were conjoined in the ventral plane with a single set of pericardial, pleural and peritoneal cavities. Internal examination revealed the presence of a common diaphragm and a single enlarged liver. Within a single central pericardium, two malformed hearts were present. Reports on this type of congenital duplication in goats have not been found in the literature. Thoracopagus and thoraco-omphalopagus are the most common types of conjoined twins in human beings and are associated with the highest mortality because of the frequent incidence of complex cardiac anatomy.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01115.x" xmlns="http://purl.org/rss/1.0/"><title>MR Anatomy of Salivary Glands in the Dog</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01115.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">MR Anatomy of Salivary Glands in the Dog</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Weidner</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Probst</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Kneissl</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-31T05:56:10.395488-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01115.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01115.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01115.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 3 figures and 2 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>This retrospective analysis documented the magnetic resonance imaging (MRI) appearance of normal salivary glands based on 101 studies in dogs with no detectable disease in the splanchnocranium. Surface, signal intensity, homogeneity, structure, symmetry and the relationship of glands to surrounding tissues were noted, and gland topography was assessed with E12 plastinated embedded sections. Signal intensity of salivary glands was isointense (7–40%) to hyperintense (60–90%) to muscle tissue on T1- and hyperintense on T2-weighted images. Salivary glands had an increased T1 signal after contrast medium was applied. Salivary gland structure appeared homogeneous in mandibular and major sublingual glands and heterogeneous in zygomatic and parotid glands. Consistent landmarks were the external auditory canal for parotid glands, the digastric muscle for mandibular and major sublingual glands, and the pterygopalatine fossa for zygomatic glands. The minor sublingual and ventral buccal glands could not be localized with low-field MRI.</p></div></div>]]></content:encoded><description>With 3 figures and 2 tablesSummaryThis retrospective analysis documented the magnetic resonance imaging (MRI) appearance of normal salivary glands based on 101 studies in dogs with no detectable disease in the splanchnocranium. Surface, signal intensity, homogeneity, structure, symmetry and the relationship of glands to surrounding tissues were noted, and gland topography was assessed with E12 plastinated embedded sections. Signal intensity of salivary glands was isointense (7–40%) to hyperintense (60–90%) to muscle tissue on T1- and hyperintense on T2-weighted images. Salivary glands had an increased T1 signal after contrast medium was applied. Salivary gland structure appeared homogeneous in mandibular and major sublingual glands and heterogeneous in zygomatic and parotid glands. Consistent landmarks were the external auditory canal for parotid glands, the digastric muscle for mandibular and major sublingual glands, and the pterygopalatine fossa for zygomatic glands. The minor sublingual and ventral buccal glands could not be localized with low-field MRI.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01116.x" xmlns="http://purl.org/rss/1.0/"><title>The Effect of Transgenesis on Rabbit Thyroid Tissue Structure</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01116.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Effect of Transgenesis on Rabbit Thyroid Tissue Structure</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Tvrda</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Massanyi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Lukac</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Danko</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Chrenek</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-31T05:56:06.693653-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01116.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01116.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01116.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SHORT COMMUNICATION</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 1 figure and 3 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>This study was aimed to compare structures of the thyroid tissue of transgenic rabbits expressing the human clotting factor VIII under the murine whey acidic protein promoter (mWAP–hFVIII rabbits) with the non-transgenic controls. Thyroid tissue samples were taken from transgenic and non-transgenic New Zealand White rabbits, examined by optical microscopy and analysed morphometrically. The analysis revealed no significant differences (<em>P</em> &gt; 0.05) in the relative volume of basic thyroid structures. Furthermore, no significant differences (<em>P</em> &gt; 0.05) were observed when measuring the epithelial height and nuclear diameter of the follicular cells. Altogether, this study demonstrates no negative effect of the mWAP–hFVIII transgenesis on the rabbit thyroid gland structure.</p></div></div>]]></content:encoded><description>With 1 figure and 3 tablesSummaryThis study was aimed to compare structures of the thyroid tissue of transgenic rabbits expressing the human clotting factor VIII under the murine whey acidic protein promoter (mWAP–hFVIII rabbits) with the non-transgenic controls. Thyroid tissue samples were taken from transgenic and non-transgenic New Zealand White rabbits, examined by optical microscopy and analysed morphometrically. The analysis revealed no significant differences (P &gt; 0.05) in the relative volume of basic thyroid structures. Furthermore, no significant differences (P &gt; 0.05) were observed when measuring the epithelial height and nuclear diameter of the follicular cells. Altogether, this study demonstrates no negative effect of the mWAP–hFVIII transgenesis on the rabbit thyroid gland structure.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01112.x" xmlns="http://purl.org/rss/1.0/"><title>Anatomical Relationship Between the Collecting System and the Intrarenal Arteries in the Rabbit: Contribution for an Experimental Model</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01112.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Anatomical Relationship Between the Collecting System and the Intrarenal Arteries in the Rabbit: Contribution for an Experimental Model</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Shalgum</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. P. S. Marques-Sampaio</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Dafalla</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. A. Pereira-Sampaio</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-23T23:37:07.935828-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01112.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01112.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01112.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 6 figures and 2 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Intrarenal anatomy was studied in detail to evaluate how useful rabbits could be as a urologic model. Only one renal artery was observed, which was divided into dorsal and ventral branches in all cases. Three segmental arteries (cranial, mesorenal and caudal) was the most frequent branching pattern found in both the dorsal and ventral division. There was an important artery related to the ureteropelvic junction in both dorsal and ventral surfaces in all specimens. The cranial pole was supplied by both dorsal and ventral divisions of the renal artery in 23 of 41 casts (56%). Although the cranial pole of the rabbit kidney could be useful as a model because of the resemblances with human kidney, the different relationship between the intrarenal arteries and the kidney collecting system in other regions of the kidney must be taken into consideration by the urologists, when using rabbit kidney in urological research.</p></div></div>]]></content:encoded><description>With 6 figures and 2 tablesSummaryIntrarenal anatomy was studied in detail to evaluate how useful rabbits could be as a urologic model. Only one renal artery was observed, which was divided into dorsal and ventral branches in all cases. Three segmental arteries (cranial, mesorenal and caudal) was the most frequent branching pattern found in both the dorsal and ventral division. There was an important artery related to the ureteropelvic junction in both dorsal and ventral surfaces in all specimens. The cranial pole was supplied by both dorsal and ventral divisions of the renal artery in 23 of 41 casts (56%). Although the cranial pole of the rabbit kidney could be useful as a model because of the resemblances with human kidney, the different relationship between the intrarenal arteries and the kidney collecting system in other regions of the kidney must be taken into consideration by the urologists, when using rabbit kidney in urological research.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01113.x" xmlns="http://purl.org/rss/1.0/"><title>NADPH-d-Positive Mast Cells in the Canine Paranal Sinus</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01113.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">NADPH-d-Positive Mast Cells in the Canine Paranal Sinus</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Stefanov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Vodenicharov</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-23T23:35:24.425844-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01113.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01113.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01113.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SHORT COMMUNICATION</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 3 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>This study aimed to investigate the enzyme histochemical expression of NADPH-d in mast cells in the wall of the paranal sinus in male and female dogs. NADPH-d-positive cells with weak, medium and strong enzyme histochemical expression were observed in the stroma of the sinus near the blood vessels of the microcirculatory bed and around the apocrine and sebaceous glands. In the same areas, mast cells with similar dimensions and morphology were demonstrated by metachromasia on paraffin and cryostat cross-sections and stained with 0.1% toluidine blue in McIlvane’s buffer (pH 3). These findings suggest that the mast cells that are located in the stroma near the blood vessels, the lining epithelium and the glands correspond with the cells with marked NADPH-d activity. The possibility of mast cells having nitric oxide activity could be used in the regulation of mast cells function when treating paranal sinus tumours and inflammations.</p></div></div>]]></content:encoded><description>With 3 figuresSummaryThis study aimed to investigate the enzyme histochemical expression of NADPH-d in mast cells in the wall of the paranal sinus in male and female dogs. NADPH-d-positive cells with weak, medium and strong enzyme histochemical expression were observed in the stroma of the sinus near the blood vessels of the microcirculatory bed and around the apocrine and sebaceous glands. In the same areas, mast cells with similar dimensions and morphology were demonstrated by metachromasia on paraffin and cryostat cross-sections and stained with 0.1% toluidine blue in McIlvane’s buffer (pH 3). These findings suggest that the mast cells that are located in the stroma near the blood vessels, the lining epithelium and the glands correspond with the cells with marked NADPH-d activity. The possibility of mast cells having nitric oxide activity could be used in the regulation of mast cells function when treating paranal sinus tumours and inflammations.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01114.x" xmlns="http://purl.org/rss/1.0/"><title>Morphometrical Variations of the Carpal Bones in Thoroughbreds and Ponies</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01114.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphometrical Variations of the Carpal Bones in Thoroughbreds and Ponies</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. H. Abdunnabi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. A. Ahmed</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. J. Philip</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. M. S. Davies</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-20T03:39:23.338634-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01114.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01114.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01114.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 5 figures and 3 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>There is scant morphological data for equine carpal bones despite the frequent pathology in Thoroughbreds (TB). This study aimed to identify morphological and morphometrical variations and similarities in carpal bones between and within TB and Ponies (Po). Carpal bones from nine TB and 13 Po were prepared by boiling and drying. Lateromedial width, dorsopalmar depth, proximodistal height, relative density and volume of each bone were measured. Normalized measurements of the radial (Cr) and third (C3) carpal bones were significantly different in all dimensions, and there were significant variations in relative sizes of articular facets of the ulnar (Cu), C3 and fourth (C4) carpal bones between the groups. Bilaterally, the proportionate volume of the intermediate carpal bone (Ci) was significantly greater in Po while that of Cu and C4 were significantly greater in TB. Relative density of most bones was greater in Po. The palmar tuberosity of the proximal surface of Ci and palmar tubercle on the palmar surface of Cu were more prominent and relatively larger in TB. In the second carpal bone (C2), the distal extent of the proximal articular surface on the palmar surface was greater in Po. The inconsistent first carpal bone (C1) was relatively larger in Po. Morphometrical similarities and differences in carpal bones between TB and Po indicate potential effects of selection for body size or fast exercise.</p></div></div>]]></content:encoded><description>With 5 figures and 3 tablesSummaryThere is scant morphological data for equine carpal bones despite the frequent pathology in Thoroughbreds (TB). This study aimed to identify morphological and morphometrical variations and similarities in carpal bones between and within TB and Ponies (Po). Carpal bones from nine TB and 13 Po were prepared by boiling and drying. Lateromedial width, dorsopalmar depth, proximodistal height, relative density and volume of each bone were measured. Normalized measurements of the radial (Cr) and third (C3) carpal bones were significantly different in all dimensions, and there were significant variations in relative sizes of articular facets of the ulnar (Cu), C3 and fourth (C4) carpal bones between the groups. Bilaterally, the proportionate volume of the intermediate carpal bone (Ci) was significantly greater in Po while that of Cu and C4 were significantly greater in TB. Relative density of most bones was greater in Po. The palmar tuberosity of the proximal surface of Ci and palmar tubercle on the palmar surface of Cu were more prominent and relatively larger in TB. In the second carpal bone (C2), the distal extent of the proximal articular surface on the palmar surface was greater in Po. The inconsistent first carpal bone (C1) was relatively larger in Po. Morphometrical similarities and differences in carpal bones between TB and Po indicate potential effects of selection for body size or fast exercise.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01111.x" xmlns="http://purl.org/rss/1.0/"><title>Gender Differences in Morphometric Properties of Muscle Fibres Measured on Cross-Sections of rat Hindlimb Muscles</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01111.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gender Differences in Morphometric Properties of Muscle Fibres Measured on Cross-Sections of rat Hindlimb Muscles</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Mierzejewska-Krzyżowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Drzymała-Celichowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Bukowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Celichowski</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-09T23:57:21.305837-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01111.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01111.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01111.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 2 figures and 2 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The study was aimed at demonstrating gender differences in the numbers, diameters and cross-section areas of muscle fibres for three hindlimb skeletal muscles responsible for locomotion and maintenance of body posture: soleus, tibialis anterior and flexor digitorum brevis in rats. The experiments were performed on five 6-month-old male and female Wistar rats. In both genders, all studied muscles of the right and left hindlimbs were isolated from surrounding tissues and excised for further procedures. The muscle transverse cross-sections taken from the muscle mid-belly were analysed. Following staining of reticular fibres by silver impregnation, the numbers, diameters and cross-section areas of muscle fibres were determined from microscopic images of muscle sections. The body mass of male rats was 80% higher than that of females. In addition, the muscle mass and the cross-section area were 53–82 and 26–45% higher in males, respectively. The number of muscle fibres was 11–42% higher in males than in females whereas the fibre diameters were 7–29% higher in males. The most conspicuous differences between males and females were found with respect to tibialis anterior, whereas the smallest differences were evident in soleus. The present study revealed that the gender morphometric differences in the studied rat hindlimb muscles were mainly owing to differences in number and size of muscle fibres and that the difference in muscle mass could be explained mainly from higher number of muscle fibres in males and to smaller degree from their larger diameters.</p></div></div>]]></content:encoded><description>With 2 figures and 2 tablesSummaryThe study was aimed at demonstrating gender differences in the numbers, diameters and cross-section areas of muscle fibres for three hindlimb skeletal muscles responsible for locomotion and maintenance of body posture: soleus, tibialis anterior and flexor digitorum brevis in rats. The experiments were performed on five 6-month-old male and female Wistar rats. In both genders, all studied muscles of the right and left hindlimbs were isolated from surrounding tissues and excised for further procedures. The muscle transverse cross-sections taken from the muscle mid-belly were analysed. Following staining of reticular fibres by silver impregnation, the numbers, diameters and cross-section areas of muscle fibres were determined from microscopic images of muscle sections. The body mass of male rats was 80% higher than that of females. In addition, the muscle mass and the cross-section area were 53–82 and 26–45% higher in males, respectively. The number of muscle fibres was 11–42% higher in males than in females whereas the fibre diameters were 7–29% higher in males. The most conspicuous differences between males and females were found with respect to tibialis anterior, whereas the smallest differences were evident in soleus. The present study revealed that the gender morphometric differences in the studied rat hindlimb muscles were mainly owing to differences in number and size of muscle fibres and that the difference in muscle mass could be explained mainly from higher number of muscle fibres in males and to smaller degree from their larger diameters.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01110.x" xmlns="http://purl.org/rss/1.0/"><title>Optimising μCT Imaging of the Middle and Inner Cat Ear</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01110.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Optimising μCT Imaging of the Middle and Inner Cat Ear</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Seifert</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">U. Röher</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Staszyk</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Angrisani</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Dziuba</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Meyer-Lindenberg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-09T23:55:24.523079-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01110.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01110.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01110.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 9 figures and 4 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>This study’s aim was to determine the optimal scan parameters for imaging the middle and inner ear of the cat with micro-computertomography (μCT). Besides, the study set out to assess whether adequate image quality can be obtained to use μCT in diagnostics and research on cat ears. For optimisation, μCT imaging of two cat skull preparations was performed using 36 different scanning protocols. The μCT-scans were evaluated by four experienced experts with regard to the image quality and detail detectability. By compiling a ranking of the results, the best possible scan parameters could be determined. From a third cat’s skull, a μCT-scan, using these optimised scan parameters, and a comparative clinical CT-scan were acquired. Afterwards, histological specimens of the ears were produced which were compared to the μCT-images. The comparison shows that the osseous structures are depicted in detail. Although soft tissues cannot be differentiated, the osseous structures serve as valuable spatial orientation of relevant nerves and muscles. Clinical CT can depict many anatomical structures which can also be seen on μCT-images, but these appear a lot less sharp and also less detailed than with μCT.</p></div></div>]]></content:encoded><description>With 9 figures and 4 tablesSummaryThis study’s aim was to determine the optimal scan parameters for imaging the middle and inner ear of the cat with micro-computertomography (μCT). Besides, the study set out to assess whether adequate image quality can be obtained to use μCT in diagnostics and research on cat ears. For optimisation, μCT imaging of two cat skull preparations was performed using 36 different scanning protocols. The μCT-scans were evaluated by four experienced experts with regard to the image quality and detail detectability. By compiling a ranking of the results, the best possible scan parameters could be determined. From a third cat’s skull, a μCT-scan, using these optimised scan parameters, and a comparative clinical CT-scan were acquired. Afterwards, histological specimens of the ears were produced which were compared to the μCT-images. The comparison shows that the osseous structures are depicted in detail. Although soft tissues cannot be differentiated, the osseous structures serve as valuable spatial orientation of relevant nerves and muscles. Clinical CT can depict many anatomical structures which can also be seen on μCT-images, but these appear a lot less sharp and also less detailed than with μCT.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01108.x" xmlns="http://purl.org/rss/1.0/"><title>Anatomical Study of the Gastrointestinal Tract of a Pudu (Pudu puda) Using Contrast-Enhanced Abdominal Computed Tomography</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01108.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Anatomical Study of the Gastrointestinal Tract of a Pudu (Pudu puda) Using Contrast-Enhanced Abdominal Computed Tomography</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. C. Henning</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. A. Gómez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L. M. Mieres</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L. Freeman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. E. Herzberg</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. A. Aleuy</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-16T09:00:59.180397-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01108.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01108.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01108.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 6 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The pudu (<em>Pudu puda</em>), which is the smallest deer in the world and inhabits central and southern Chile and Argentina, is a ruminant and a browsing herbivore. The aim of this study was to provide a reference for interpretation of the normal anatomy of the pudu’s gastrointestinal tract as imaged by abdominal computed tomography (CT). For the study, one adult female pudu was used. After a 24-h fast, the pudu was anaesthetized and positioned in sternal recumbency at the CT table. Image acquisition began immediately after intravenous injection of contrast media (MD-76<sup>®</sup>; 370 mgI/ml) into the cephalic vein. Injection of contrast material was administered as a biphasic protocol. First, a manual bolus of contrast material was injected at a rate of 4 ml/s. Then, an additional continuous infusion injection (0.1 ml/min) was performed for adequate opacification of vascular structures. Transverse images of 5 mm thickness and 5 mm interval were obtained with a fourth-generation CT scanner, from the ninth thoracic vertebra (T9) until the first sacral (S1) vertebrae. CT images were labelled and compared with anatomical reference images for ruminants. Structures that were identified in the abdominal cavity included the stomach with its four compartments (rumen, reticulum, omasum and abomasum), the small and large intestines, liver, spleen, kidneys and some major blood vessels (aorta, caudal vena cava). The distal loop of the ascending colon, the transverse colon, the pancreas and lymph nodes could not be identified. The resulting CT images provide a reference for normal cross-sectional abdominal anatomy of the adult pudu.</p></div></div>]]></content:encoded><description>With 6 figuresSummaryThe pudu (Pudu puda), which is the smallest deer in the world and inhabits central and southern Chile and Argentina, is a ruminant and a browsing herbivore. The aim of this study was to provide a reference for interpretation of the normal anatomy of the pudu’s gastrointestinal tract as imaged by abdominal computed tomography (CT). For the study, one adult female pudu was used. After a 24-h fast, the pudu was anaesthetized and positioned in sternal recumbency at the CT table. Image acquisition began immediately after intravenous injection of contrast media (MD-76®; 370 mgI/ml) into the cephalic vein. Injection of contrast material was administered as a biphasic protocol. First, a manual bolus of contrast material was injected at a rate of 4 ml/s. Then, an additional continuous infusion injection (0.1 ml/min) was performed for adequate opacification of vascular structures. Transverse images of 5 mm thickness and 5 mm interval were obtained with a fourth-generation CT scanner, from the ninth thoracic vertebra (T9) until the first sacral (S1) vertebrae. CT images were labelled and compared with anatomical reference images for ruminants. Structures that were identified in the abdominal cavity included the stomach with its four compartments (rumen, reticulum, omasum and abomasum), the small and large intestines, liver, spleen, kidneys and some major blood vessels (aorta, caudal vena cava). The distal loop of the ascending colon, the transverse colon, the pancreas and lymph nodes could not be identified. The resulting CT images provide a reference for normal cross-sectional abdominal anatomy of the adult pudu.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01107.x" xmlns="http://purl.org/rss/1.0/"><title>Microscopic Anatomy of the Lower Respiratory Tract of the Grey Short-Tailed Opossum (Monodelphis domestica)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01107.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Microscopic Anatomy of the Lower Respiratory Tract of the Grey Short-Tailed Opossum (Monodelphis domestica)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L. A. Cope</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. W. Henry</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. B. Reed</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-15T09:29:49.734651-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01107.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01107.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01107.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 14 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The respiratory tracts of seven grey short-tailed opossums were histologically examined. Six opossums were prepared by perfusion with buffered formalin. Opossum seven was perfused with gluteraldehyde. Samples taken from the respiratory passages and lungs of specimens 1–6 were stained with haematoxylin and eosin. A mixture of methylene and azure blue was used for specimen 7. The trachea and right and left principal bronchi are lined with a pseudostratified ciliated columnar epithelium with occasional goblet cells. The secondary and tertiary bronchi and the primary and secondary bronchioles are lined by a simple ciliated columnar epithelium. The terminal bronchioles and a portion of the respiratory bronchioles are lined by a simple ciliated cuboidal epithelium. The terminal portion of the respiratory bronchioles and the alveolar ducts are lined with simple squamous epithelium. Alveoli are lined by type I and II pneumocytes. Tracheal glands are present in the tela submucosa. The fibromusculocartilaginous tunic of the trachea consists of c-shaped cartilage rings and the trachealis muscle. A lamina muscularis mucosa begins in the intrapulmonary portion of the principal bronchus and continues into the respiratory bronchioles. Bronchial glands are present in the propria submucosa and tela submucosa of the principal bronchi. The musculocartilaginous tunic is localized to the extrapulmonary portion of the principal bronchus. The bronchial cartilages are irregular shaped plates and limited to the extrapulmonary portion of the principal bronchus. The visceral pleura is a simple squamous mesothelium covering the outer surface of the lung.</p></div></div>]]></content:encoded><description>With 14 figuresSummaryThe respiratory tracts of seven grey short-tailed opossums were histologically examined. Six opossums were prepared by perfusion with buffered formalin. Opossum seven was perfused with gluteraldehyde. Samples taken from the respiratory passages and lungs of specimens 1–6 were stained with haematoxylin and eosin. A mixture of methylene and azure blue was used for specimen 7. The trachea and right and left principal bronchi are lined with a pseudostratified ciliated columnar epithelium with occasional goblet cells. The secondary and tertiary bronchi and the primary and secondary bronchioles are lined by a simple ciliated columnar epithelium. The terminal bronchioles and a portion of the respiratory bronchioles are lined by a simple ciliated cuboidal epithelium. The terminal portion of the respiratory bronchioles and the alveolar ducts are lined with simple squamous epithelium. Alveoli are lined by type I and II pneumocytes. Tracheal glands are present in the tela submucosa. The fibromusculocartilaginous tunic of the trachea consists of c-shaped cartilage rings and the trachealis muscle. A lamina muscularis mucosa begins in the intrapulmonary portion of the principal bronchus and continues into the respiratory bronchioles. Bronchial glands are present in the propria submucosa and tela submucosa of the principal bronchi. The musculocartilaginous tunic is localized to the extrapulmonary portion of the principal bronchus. The bronchial cartilages are irregular shaped plates and limited to the extrapulmonary portion of the principal bronchus. The visceral pleura is a simple squamous mesothelium covering the outer surface of the lung.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01106.x" xmlns="http://purl.org/rss/1.0/"><title>Normal Feline Brain: Clinical Anatomy Using Magnetic Resonance Imaging</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01106.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Normal Feline Brain: Clinical Anatomy Using Magnetic Resonance Imaging</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Mogicato</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Conchou</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Layssol-Lamour</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Raharison</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Sautet</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-15T09:29:35.160528-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01106.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01106.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01106.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 6 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The purpose of this study was to provide a clinical anatomy atlas of the feline brain using magnetic resonance imaging (MRI). Brains of twelve normal cats were imaged using a 1.5 T magnetic resonance unit and an inversion/recovery sequence (T1). Fourteen relevant MRI sections were chosen in transverse, dorsal, median and sagittal planes. Anatomic structures were identified and labelled using anatomical texts and <em>Nomina Anatomica Veterinaria</em>, sectioned specimen heads, and previously published articles. The MRI sections were stained according to the major embryological and anatomical subdivisions of the brain. The relevant anatomical structures seen on MRI will assist clinicians to better understand MR images and to relate this neuro-anatomy to clinical signs.</p></div></div>]]></content:encoded><description>With 6 figuresSummaryThe purpose of this study was to provide a clinical anatomy atlas of the feline brain using magnetic resonance imaging (MRI). Brains of twelve normal cats were imaged using a 1.5 T magnetic resonance unit and an inversion/recovery sequence (T1). Fourteen relevant MRI sections were chosen in transverse, dorsal, median and sagittal planes. Anatomic structures were identified and labelled using anatomical texts and Nomina Anatomica Veterinaria, sectioned specimen heads, and previously published articles. The MRI sections were stained according to the major embryological and anatomical subdivisions of the brain. The relevant anatomical structures seen on MRI will assist clinicians to better understand MR images and to relate this neuro-anatomy to clinical signs.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01105.x" xmlns="http://purl.org/rss/1.0/"><title>An Immunohistochemical Study of Ovarian Follicle Histogenesis in the Early Post-hatch Japanese Quail (Coturnix coturnix japonica)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01105.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An Immunohistochemical Study of Ovarian Follicle Histogenesis in the Early Post-hatch Japanese Quail (Coturnix coturnix japonica)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M.-C. Madekurozwa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-15T09:28:37.555175-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01105.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01105.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01105.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 6 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The early post-hatch development of immunoreactivity to vimentin, desmin, smooth muscle actin (SMA) and laminin, in relation to follicle histogenesis, was described in this study. Ovigerous cords in day old quails contained pre-granulosa cells and oocytes. Pre-granulosa cells at the cortico-medullary junction were vimentin immunopositive. A laminin immunopositive basement membrane and desmin immunopositive mesenchymal cells lined the ovigerous cords. Ovigerous cords in 3-day-old quails contained developing primordial follicles, the vimentin immunopositive pre-granulosa cells of which were partially encircled by a basement membrane and desmin immunopositive mesenchymal cells. In 5- to 7-day-old quails, ovigerous cords formed an outer cortical region, while primordial follicles formed the inner cortical region. Early pre-vitellogenic follicles were present in 9- to 13-day-old quails. Underlying the granulosa cells of these follicles was a laminin immunopositive basement membrane and a layer of desmin immunopositive thecal cells. Early and late pre-vitellogenic follicles dominated the ovary in 15- to 17-day-old quails. The thecal layer in these follicles was desmin immunopositive, but SMA immunonegative. The results of the study have shown that the process of primordial follicle development in the Japanese quail is similar to that reported in mammals. The study suggests that in the quail pre-granulosa cells originate predominantly from the medulla. The study has shown that, in the Japanese quail, thecal cells are derived from desmin immunopositive mesenchymal cells lining the ovigerous cords.</p></div></div>]]></content:encoded><description>With 6 figuresSummaryThe early post-hatch development of immunoreactivity to vimentin, desmin, smooth muscle actin (SMA) and laminin, in relation to follicle histogenesis, was described in this study. Ovigerous cords in day old quails contained pre-granulosa cells and oocytes. Pre-granulosa cells at the cortico-medullary junction were vimentin immunopositive. A laminin immunopositive basement membrane and desmin immunopositive mesenchymal cells lined the ovigerous cords. Ovigerous cords in 3-day-old quails contained developing primordial follicles, the vimentin immunopositive pre-granulosa cells of which were partially encircled by a basement membrane and desmin immunopositive mesenchymal cells. In 5- to 7-day-old quails, ovigerous cords formed an outer cortical region, while primordial follicles formed the inner cortical region. Early pre-vitellogenic follicles were present in 9- to 13-day-old quails. Underlying the granulosa cells of these follicles was a laminin immunopositive basement membrane and a layer of desmin immunopositive thecal cells. Early and late pre-vitellogenic follicles dominated the ovary in 15- to 17-day-old quails. The thecal layer in these follicles was desmin immunopositive, but SMA immunonegative. The results of the study have shown that the process of primordial follicle development in the Japanese quail is similar to that reported in mammals. The study suggests that in the quail pre-granulosa cells originate predominantly from the medulla. The study has shown that, in the Japanese quail, thecal cells are derived from desmin immunopositive mesenchymal cells lining the ovigerous cords.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01096.x" xmlns="http://purl.org/rss/1.0/"><title>Expression of Oestrogen Receptors in Foetal Lung Tissue of Mice</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01096.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Expression of Oestrogen Receptors in Foetal Lung Tissue of Mice</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Carvalho</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Gonçalves</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01096.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01096.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01096.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">6</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 2 figures and 1 table</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Oestrogens are responsible for the sexual dimorphism in adult mice lung tissue, and this difference is most notable at sexual maturity. Oestrogen receptor-alpha (ERα) and the oestrogen receptor-beta (ERβ) are the two receptors that mediate oestrogen action, but adult mice lung tissue only expresses ERβ, and it is probably through this receptor that oestrogens exert their action. The goal of our study was to detect the expression of ERα and ERβ in mouse foetal lung tissues and identify possible gender differences. The foetal lung tissue was collected between developmental days E15–E19, processed for histology and the expression of oestrogen receptors was detected by immunohistochemistry. Over the 5 days of lung development that were evaluated ERα was not expressed in the foetal lung tissues of neither male nor female mice. In contrast, ERβ was detected in both sexes, although the immunoreactivity differed for each developmental day whilst the staining intensity observed for ERβ also indicated differences between male and female lung tissues. The results demonstrate the existence of a gender difference in the foetal expression of ERβ in lungs of mice.</p></div></div>]]></content:encoded><description>With 2 figures and 1 tableSummaryOestrogens are responsible for the sexual dimorphism in adult mice lung tissue, and this difference is most notable at sexual maturity. Oestrogen receptor-alpha (ERα) and the oestrogen receptor-beta (ERβ) are the two receptors that mediate oestrogen action, but adult mice lung tissue only expresses ERβ, and it is probably through this receptor that oestrogens exert their action. The goal of our study was to detect the expression of ERα and ERβ in mouse foetal lung tissues and identify possible gender differences. The foetal lung tissue was collected between developmental days E15–E19, processed for histology and the expression of oestrogen receptors was detected by immunohistochemistry. Over the 5 days of lung development that were evaluated ERα was not expressed in the foetal lung tissues of neither male nor female mice. In contrast, ERβ was detected in both sexes, although the immunoreactivity differed for each developmental day whilst the staining intensity observed for ERβ also indicated differences between male and female lung tissues. The results demonstrate the existence of a gender difference in the foetal expression of ERβ in lungs of mice.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01097.x" xmlns="http://purl.org/rss/1.0/"><title>Ultrasonographic and Macroscopic Anatomy of the Enucleated Eyes of the Buffalo (Bos bubalis) and the One-Humped Camel (Camelus dromedarius) of Different Ages</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01097.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ultrasonographic and Macroscopic Anatomy of the Enucleated Eyes of the Buffalo (Bos bubalis) and the One-Humped Camel (Camelus dromedarius) of Different Ages</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Kassab</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01097.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01097.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01097.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">7</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">11</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 1 figure and 2 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The ultrasonographic appearance and measurements of the normal buffalo and camel eye globes were described in 60 buffaloes (<em>Bos bubalis</em>) aged 1 year (28 eyes) and 10 years (32 eyes), and in 51 humped camels (<em>Camelus dromedarius</em>) aged 1 year (26 eyes) and 10 years (24 eyes). Ocular measurements were recorded by A- and B-scan ultrasonographic examination of 40 buffalo eyes (18 young and 22 adult eyes) and 34 camel eyes (14 young and 20 adult eyes) using a KANGH ultrasound scanner equipped with 10 MHz probe. For gross measurements, 20 buffalo and 16 camel eye globes were frozen and dissected and the same measurements were made using fine callipers macroscopically. The aqueous and vitreous humour of the buffalo and camel eyes appeared anechoic. The cornea, anterior and posterior lens capsule and iris appeared hyperechoic. The ocular measurements for the axial length, vitreous chamber depth (VCD), corneal thickness, lens thickness and scleroretinal rim thickness increase with the advance of age in both buffaloes and camels. Except for the anterior chamber depth, VCD and lens thickness, which were larger in adult camels than in adult buffaloes, no other differences between ocular dimensions were observed in both species. The results of this study are valuable for comparative ocular anatomy and will be useful for ultrasonographic evaluation of ocular diseases in buffaloes and camels.</p></div></div>]]></content:encoded><description>With 1 figure and 2 tablesSummaryThe ultrasonographic appearance and measurements of the normal buffalo and camel eye globes were described in 60 buffaloes (Bos bubalis) aged 1 year (28 eyes) and 10 years (32 eyes), and in 51 humped camels (Camelus dromedarius) aged 1 year (26 eyes) and 10 years (24 eyes). Ocular measurements were recorded by A- and B-scan ultrasonographic examination of 40 buffalo eyes (18 young and 22 adult eyes) and 34 camel eyes (14 young and 20 adult eyes) using a KANGH ultrasound scanner equipped with 10 MHz probe. For gross measurements, 20 buffalo and 16 camel eye globes were frozen and dissected and the same measurements were made using fine callipers macroscopically. The aqueous and vitreous humour of the buffalo and camel eyes appeared anechoic. The cornea, anterior and posterior lens capsule and iris appeared hyperechoic. The ocular measurements for the axial length, vitreous chamber depth (VCD), corneal thickness, lens thickness and scleroretinal rim thickness increase with the advance of age in both buffaloes and camels. Except for the anterior chamber depth, VCD and lens thickness, which were larger in adult camels than in adult buffaloes, no other differences between ocular dimensions were observed in both species. The results of this study are valuable for comparative ocular anatomy and will be useful for ultrasonographic evaluation of ocular diseases in buffaloes and camels.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01099.x" xmlns="http://purl.org/rss/1.0/"><title>Computed Tomographical (CT) Anatomy of the Thoracoabdominal Cavity of the Male Turkey (Meleagris gallopavo)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01099.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Computed Tomographical (CT) Anatomy of the Thoracoabdominal Cavity of the Male Turkey (Meleagris gallopavo)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Petnehazy</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Benczik</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Takacs</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zs. Petrasi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Z. Sütő</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Horn</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Repa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01099.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01099.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01099.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">12</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">20</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 10 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>In the present work, our goal was to match high-resolution computed tomography (CT) scans with cross-sectional anatomical pictures of the turkey (<em>Meleagris gallopavo</em>). Two male BUT 6 (a commercial line) turkeys were used. CT scans with 1 mm slice thickness were performed. The images covered the trunk from the level of the 9th cervical vertebra to the end of the coccyx. The anatomical sections and the CT scans were matched, and the important structures were identified and labelled on the corresponding pictures. The aim of this study was to create a reference for evaluating CT scans of avian species.</p></div></div>]]></content:encoded><description>With 10 figuresSummaryIn the present work, our goal was to match high-resolution computed tomography (CT) scans with cross-sectional anatomical pictures of the turkey (Meleagris gallopavo). Two male BUT 6 (a commercial line) turkeys were used. CT scans with 1 mm slice thickness were performed. The images covered the trunk from the level of the 9th cervical vertebra to the end of the coccyx. The anatomical sections and the CT scans were matched, and the important structures were identified and labelled on the corresponding pictures. The aim of this study was to create a reference for evaluating CT scans of avian species.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01098.x" xmlns="http://purl.org/rss/1.0/"><title>Skeleton Pattern and Joint Formation in Chorioallantoic Grafts Containing the Distal Parts of the Chick Wing Bud</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01098.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skeleton Pattern and Joint Formation in Chorioallantoic Grafts Containing the Distal Parts of the Chick Wing Bud</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Rizgeliene</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Tutkuviene</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01098.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01098.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01098.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">21</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">30</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 13 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Skeleton pattern formation was examined in chick wing bud grafts using the chorioallantoic grafting method. The distal parts of the wing bud were excised from the donor wing and transplanted onto the chorioallantoic membrane (the experimental groups). Transplants with intact limb bud material served as the control group. The skeleton pattern formation in the grafts depended on the amount of transplanted material and donor’s limb bud stage. The younger the donor’s stage and the bigger the piece of the transplanted material the more proximal parts grafts had, more retarded growth and abnormal skeleton in the zeugopod and autopod was. The percentage of the signs of insufficient blood supply in the experimental groups was less than that in the control group. As the amount of the transplanted limb bud material decreased and donor’s limb bud aged, post-axial polydactyly changed to the pre-axial one.</p></div></div>]]></content:encoded><description>With 13 figuresSummarySkeleton pattern formation was examined in chick wing bud grafts using the chorioallantoic grafting method. The distal parts of the wing bud were excised from the donor wing and transplanted onto the chorioallantoic membrane (the experimental groups). Transplants with intact limb bud material served as the control group. The skeleton pattern formation in the grafts depended on the amount of transplanted material and donor’s limb bud stage. The younger the donor’s stage and the bigger the piece of the transplanted material the more proximal parts grafts had, more retarded growth and abnormal skeleton in the zeugopod and autopod was. The percentage of the signs of insufficient blood supply in the experimental groups was less than that in the control group. As the amount of the transplanted limb bud material decreased and donor’s limb bud aged, post-axial polydactyly changed to the pre-axial one.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01100.x" xmlns="http://purl.org/rss/1.0/"><title>Coxa Morphologically Adapted to Large Egg in Aepyornithid Species Compared with Various Palaeognaths</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01100.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Coxa Morphologically Adapted to Large Egg in Aepyornithid Species Compared with Various Palaeognaths</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Endo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Akishinonomiya</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Yonezawa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Hasegawa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Rakotondraparany</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Sasaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Taru</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Yoshida</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Yamasaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Itou</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Koie</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Sakai</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01100.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01100.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01100.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">31</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">40</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 12 figures and 3 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The coxa of palaeognaths including extinct aepyornithid species was compared by means of osteology, computed tomography (CT) imaging and macroscopic anatomy. The pre-acetabular area of the ilium was proportionally much larger in width and height in aepyornithid species than in other extant palaeognaths. The post-acetabular area of the ilium, ischium and pubis was relatively short and bilaterally extended in aepyornithid species. Although the <em>Aepyornis</em> species might have produced egg with a major axis exceeding 300 mm in major axis, the short post-acetabular coxa and widely opened ischium and pubis would not have been able to stably hold the eggs in the posterior space of the pelvic cavity unlike the situation in the ostrich. As aepyornithid species resembled the kiwi in measurement ratios of length and width in the pre-acetabular area, a functional–morphological model of the coxa in the aepyornithid species can be proposed based on that of the kiwi. From our data, we suggest that the extinct species of <em>Aepyornis</em> and <em>Mullerornis</em> species effectively used the anterior space of the pelvic cavity to support their extraordinary large egg.</p></div></div>]]></content:encoded><description>With 12 figures and 3 tablesSummaryThe coxa of palaeognaths including extinct aepyornithid species was compared by means of osteology, computed tomography (CT) imaging and macroscopic anatomy. The pre-acetabular area of the ilium was proportionally much larger in width and height in aepyornithid species than in other extant palaeognaths. The post-acetabular area of the ilium, ischium and pubis was relatively short and bilaterally extended in aepyornithid species. Although the Aepyornis species might have produced egg with a major axis exceeding 300 mm in major axis, the short post-acetabular coxa and widely opened ischium and pubis would not have been able to stably hold the eggs in the posterior space of the pelvic cavity unlike the situation in the ostrich. As aepyornithid species resembled the kiwi in measurement ratios of length and width in the pre-acetabular area, a functional–morphological model of the coxa in the aepyornithid species can be proposed based on that of the kiwi. From our data, we suggest that the extinct species of Aepyornis and Mullerornis species effectively used the anterior space of the pelvic cavity to support their extraordinary large egg.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01101.x" xmlns="http://purl.org/rss/1.0/"><title>Seasonal Changes in the Histochemical Properties of the Olfactory Epithelium and Vomeronasal Organ in the Japanese Striped Snake, Elaphe quadrivirgata</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01101.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seasonal Changes in the Histochemical Properties of the Olfactory Epithelium and Vomeronasal Organ in the Japanese Striped Snake, Elaphe quadrivirgata</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Kondoh</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Yamamoto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Nakamuta</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Taniguchi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Taniguchi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01101.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01101.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01101.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">41</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">53</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 5 figures and 5 tables</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Seasonal changes in the histochemical properties of the vomeronasal and olfactory epithelia of the Japanese striped snake were examined in four seasons, viz. the reproductive, pre-hibernating, hibernating and post-hibernating seasons. In the vomeronasal and olfactory supporting cells, secretory granules were much more abundant in the hibernating season than in the other seasons. In the vomeronasal and olfactory receptor cells, the lipofuscin granules were much fewer in the post-hibernating season than in the other seasons. In histochemical studies with 21 lectins, several lectins stained the vomeronasal and olfactory epithelia (receptor cells, supporting cells and free border) more weakly in the hibernating season than in the reproductive season. However, all lectins stained both epithelia in the hibernating season after sialic acid removal in a similar manner as in the reproductive season after sialic acid removal. These lectin histochemical studies indicate that sialic acid residues in the vomeronasal and olfactory epithelia are more numerous in the hibernating season than in the reproductive season. The results suggest that during hibernation, the vomeronasal and olfactory receptor cells possibly undergo rapid cell turnover, and that during this time, the vomeronasal and olfactory epithelia are securely protected from pathogens by an innate immune defence system.</p></div></div>]]></content:encoded><description>With 5 figures and 5 tablesSummarySeasonal changes in the histochemical properties of the vomeronasal and olfactory epithelia of the Japanese striped snake were examined in four seasons, viz. the reproductive, pre-hibernating, hibernating and post-hibernating seasons. In the vomeronasal and olfactory supporting cells, secretory granules were much more abundant in the hibernating season than in the other seasons. In the vomeronasal and olfactory receptor cells, the lipofuscin granules were much fewer in the post-hibernating season than in the other seasons. In histochemical studies with 21 lectins, several lectins stained the vomeronasal and olfactory epithelia (receptor cells, supporting cells and free border) more weakly in the hibernating season than in the reproductive season. However, all lectins stained both epithelia in the hibernating season after sialic acid removal in a similar manner as in the reproductive season after sialic acid removal. These lectin histochemical studies indicate that sialic acid residues in the vomeronasal and olfactory epithelia are more numerous in the hibernating season than in the reproductive season. The results suggest that during hibernation, the vomeronasal and olfactory receptor cells possibly undergo rapid cell turnover, and that during this time, the vomeronasal and olfactory epithelia are securely protected from pathogens by an innate immune defence system.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01102.x" xmlns="http://purl.org/rss/1.0/"><title>Immunohistochemical Aspects of Anti-microbial Properties in Goat Submandibular Glands</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01102.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Immunohistochemical Aspects of Anti-microbial Properties in Goat Submandibular Glands</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Habata</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Yasui</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Fujimori</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Tsukise</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01102.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01102.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01102.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">54</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">59</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 7 figures and 1 table</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Salivary glands are known as the principal source of anti-microbial substances, which are considered to be essential components of saliva. The distribution of anti-microbial substances in the submandibular glands of Japanese miniature (Shiba) goat was studied using immunohistochemical methods as performed by physical development procedures. In the goat, anti-microbial substances such as lysozyme, IgA, lactoferrin and β-defensin were demonstrated to be immunolocalized in the submandibular glands, especially in the serous demilunes and duct cells. The results obtained are discussed with regard to the specific functions of the saliva. The presence and secretion of anti-microbial substances suggest that they participate in the maintenance of oral health among the elements of saliva.</p></div></div>]]></content:encoded><description>With 7 figures and 1 tableSummarySalivary glands are known as the principal source of anti-microbial substances, which are considered to be essential components of saliva. The distribution of anti-microbial substances in the submandibular glands of Japanese miniature (Shiba) goat was studied using immunohistochemical methods as performed by physical development procedures. In the goat, anti-microbial substances such as lysozyme, IgA, lactoferrin and β-defensin were demonstrated to be immunolocalized in the submandibular glands, especially in the serous demilunes and duct cells. The results obtained are discussed with regard to the specific functions of the saliva. The presence and secretion of anti-microbial substances suggest that they participate in the maintenance of oral health among the elements of saliva.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01104.x" xmlns="http://purl.org/rss/1.0/"><title>Magnetic Resonance Imaging of Normal Nasal Cavity and Paranasal Sinuses in Cats</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01104.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Magnetic Resonance Imaging of Normal Nasal Cavity and Paranasal Sinuses in Cats</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Conchou</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Sautet</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Raharison</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Mogicato</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01104.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01104.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01104.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">60</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">67</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 6 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>A detailed description of the nasal cavity and paranasal sinuses in clinically normal cats using magnetic resonance imaging (MRI) is presented. The heads of seven normal cats were imaged using a 1.5-T MR unit and two sequences spin echo (SE) T1-weighted and fast spin echo (FSE) T2-weighted. Eighteen relevant MR scans were taken in the transverse (12 scans) and dorsal (six scans) planes. Anatomical structures were identified and labelled using anatomical texts, sectioned specimen heads and previous studies. MR scans revealed the soft-tissue structure of the head. Identified relevant anatomical structures seen on MRI will assist clinicians to better understand MR images and evaluate pathological conditions that affect the nasal region.</p></div></div>]]></content:encoded><description>With 6 figuresSummaryA detailed description of the nasal cavity and paranasal sinuses in clinically normal cats using magnetic resonance imaging (MRI) is presented. The heads of seven normal cats were imaged using a 1.5-T MR unit and two sequences spin echo (SE) T1-weighted and fast spin echo (FSE) T2-weighted. Eighteen relevant MR scans were taken in the transverse (12 scans) and dorsal (six scans) planes. Anatomical structures were identified and labelled using anatomical texts, sectioned specimen heads and previous studies. MR scans revealed the soft-tissue structure of the head. Identified relevant anatomical structures seen on MRI will assist clinicians to better understand MR images and evaluate pathological conditions that affect the nasal region.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01103.x" xmlns="http://purl.org/rss/1.0/"><title>Development of Collagen Fibres and Lysyl Oxidase Expression in the Presumptive Dermis of Chick Limb Bud</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01103.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Development of Collagen Fibres and Lysyl Oxidase Expression in the Presumptive Dermis of Chick Limb Bud</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Yamazaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Mikami</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Yuguchi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Namba</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Isokawa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01103.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01103.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01103.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">68</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">74</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 4 figures and 1 table</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>Lysyl oxidase (LOX) plays a critical role in the formation of cross-linkages in extracellular matrix molecules. Thus, it is essential for the biogenesis and homeostasis of the connective tissue matrix. During development, collagen fibres and elastic system fibres emerge and accumulate in a temporospatial manner in the presumptive dermis of chicks. In this study, we investigated LOX mRNA expression by laser capture microdissection and RT-qPCR and LOX protein localization by immunohistochemistry. The picrosirius polarization method was used to investigate a relation between collagen accumulation and LOX expression. PCR analysis showed that the expression of LOX mRNA in the presumptive dermis became apparent at embryonic day 13 and increased considerably by ED17. Immunohistochemical staining for LOX in the dermis was very low at all stages of development. Accumulation of collagen fibres was seen in the dermis on ED10, and higher wavelengths of birefringence became evident by ED13. Our findings suggest that the temporal pattern of LOX mRNA expression correlates with collagen fibre accumulation in the dermis of the developing chick limb bud, whereas LOX expression was relatively constant at the protein level.</p></div></div>]]></content:encoded><description>With 4 figures and 1 tableSummaryLysyl oxidase (LOX) plays a critical role in the formation of cross-linkages in extracellular matrix molecules. Thus, it is essential for the biogenesis and homeostasis of the connective tissue matrix. During development, collagen fibres and elastic system fibres emerge and accumulate in a temporospatial manner in the presumptive dermis of chicks. In this study, we investigated LOX mRNA expression by laser capture microdissection and RT-qPCR and LOX protein localization by immunohistochemistry. The picrosirius polarization method was used to investigate a relation between collagen accumulation and LOX expression. PCR analysis showed that the expression of LOX mRNA in the presumptive dermis became apparent at embryonic day 13 and increased considerably by ED17. Immunohistochemical staining for LOX in the dermis was very low at all stages of development. Accumulation of collagen fibres was seen in the dermis on ED10, and higher wavelengths of birefringence became evident by ED13. Our findings suggest that the temporal pattern of LOX mRNA expression correlates with collagen fibre accumulation in the dermis of the developing chick limb bud, whereas LOX expression was relatively constant at the protein level.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01109.x" xmlns="http://purl.org/rss/1.0/"><title>The Structure of the Atrioventricular Node in the Heart of the Female Laying Ostrich (Struthio camelus)</title><link>http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01109.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Structure of the Atrioventricular Node in the Heart of the Female Laying Ostrich (Struthio camelus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Parto</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1439-0264.2011.01109.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1439-0264.2011.01109.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1439-0264.2011.01109.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">75</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">78</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>With 5 figures</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Summary</h3><div class="para"><p>The electrical impulse for cardiac contraction is generated in the Sinoatrial node (SA node), subsequently spreads to the Atrioventricular node (AV node) and continues in the Atrioventricular bundle (AV bundle). The AV node may not always be present in different avian species and seems to differ in location and contents between species. In this study, the anatomy and histology of the AV node were studied five female adult ostriches (<em>Struthio camelus</em>). Routine paraffin sectioning and transmission electron microscopic method were performed. The study showed that in the ostrich, the AV node is located in the endocardium of the atrial surface of the right atrioventricular valve adjacent to the fibrous ring. The parenchyma of the AV node is formed by small specialized muscle fibres that are spread within a loose connective tissue network. The AV node is not covered by a connective tissue sheath and some arterioles are present. Nerve fibres are seen related to the node. Ultrastructurally, they stain lighter and contain fewer organized myofibrils than usual myocardial cells. The myofibril bundles run parallel to one another and have interspersed mitochondria, which display distinct cristae. The cells have a large euchromatic nucleus with a clear perinuclear area, and they connected by desmosomes. The ostrich is, thus, one of the birds that have the AV node, whose position varies from the other birds.</p></div></div>]]></content:encoded><description>With 5 figuresSummaryThe electrical impulse for cardiac contraction is generated in the Sinoatrial node (SA node), subsequently spreads to the Atrioventricular node (AV node) and continues in the Atrioventricular bundle (AV bundle). The AV node may not always be present in different avian species and seems to differ in location and contents between species. In this study, the anatomy and histology of the AV node were studied five female adult ostriches (Struthio camelus). Routine paraffin sectioning and transmission electron microscopic method were performed. The study showed that in the ostrich, the AV node is located in the endocardium of the atrial surface of the right atrioventricular valve adjacent to the fibrous ring. The parenchyma of the AV node is formed by small specialized muscle fibres that are spread within a loose connective tissue network. The AV node is not covered by a connective tissue sheath and some arterioles are present. Nerve fibres are seen related to the node. Ultrastructurally, they stain lighter and contain fewer organized myofibrils than usual myocardial cells. The myofibril bundles run parallel to one another and have interspersed mitochondria, which display distinct cristae. The cells have a large euchromatic nucleus with a clear perinuclear area, and they connected by desmosomes. The ostrich is, thus, one of the birds that have the AV node, whose position varies from the other birds.</description></item></rdf:RDF>
