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There are 1944 results for: content related to: Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene

  1. Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma

    Genes, Chromosomes and Cancer

    Volume 33, Issue 3, March 2002, Pages: 285–294, Katharina Wimmer, Xiao-xiang Zhu, Jean Marie Rouillard, Peter F. Ambros, Barbara J. Lamb, Rork Kuick, Markus Eckart, Andreas Weinhäusl, Christa Fonatsch and Sam M. Hanash

    Version of Record online : 1 FEB 2002, DOI: 10.1002/gcc.10030

  2. Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 236–244, Hülya Kayserili, U. Altunoglu, H. Ozgur, S. Basaran and Z.O. Uyguner

    Version of Record online : 2 DEC 2011, DOI: 10.1002/ajmg.a.34390

  3. Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia

    Clinical Genetics

    Volume 91, Issue 3, March 2017, Pages: 494–498, A. Ullah, U.-E Kalsoom, M. Umair, P. John, M. Ansar, S. Basit and W. Ahmad

    Version of Record online : 12 JUL 2016, DOI: 10.1111/cge.12822

  4. You have full text access to this OnlineOpen article
    Gnawing at striping – how rodents evolve striped patterns

    Pigment Cell & Melanoma Research

    Volume 30, Issue 2, March 2017, Pages: 181–182, Robert N. Kelsh and Kleio Petratou

    Version of Record online : 7 MAR 2017, DOI: 10.1111/pcmr.12580

  5. Modeling anterior development in mice: Diet as modulator of risk for neural tube defects

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 163, Issue 4, November 2013, Pages: 333–356, Claudia Kappen

    Version of Record online : 4 OCT 2013, DOI: 10.1002/ajmg.c.31380

  6. Potocki–shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype

    American Journal of Medical Genetics Part A

    Volume 164, Issue 2, February 2014, Pages: 346–352, Alessandra Ferrarini, Muriel Gaillard, Frederic Guerry, Gianpaolo Ramelli, Fodstad Heidi, Caroline Verley Keddache, Ilse Wieland, Jacques S. Beckmann, Sébastien Jaquemont and Danielle Martinet

    Version of Record online : 13 DEC 2013, DOI: 10.1002/ajmg.a.36140

  7. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1233–1235, Lucilene Arilho Ribeiro-Bicudo, Rodrigo G. Quiezi, Maria Leine Guion-Almeida, Chiara Legnaro and Antonio Richieri-Costa

    Version of Record online : 11 APR 2012, DOI: 10.1002/ajmg.a.35305

  8. Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 600–604, Débora R Bertola, Melina G. Rodrigues, Caio R.D.C. Quaio, Chong A. Kim and Maria Rita Passos-Bueno

    Version of Record online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35762

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    Epigenetic silencing of Aristaless-like homeobox-4, a potential tumor suppressor gene associated with lung cancer

    International Journal of Cancer

    Volume 134, Issue 6, 15 March 2014, Pages: 1311–1322, Wen-Bin Liu, Fei Han, Xing-Hua Du, Xiao Jiang, Yong-Hong Li, Yong Liu, Hong-Qiang Chen, Lin Ao, Zhi-Hong Cui, Jia Cao and Jin-Yi Liu

    Version of Record online : 11 NOV 2013, DOI: 10.1002/ijc.28472

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    Molecular mechanisms of midfacial developmental defects

    Developmental Dynamics

    Volume 245, Issue 3, March 2016, Pages: 276–293, Akiko Suzuki, Dhruvee R. Sangani, Afreen Ansari and Junichi Iwata

    Version of Record online : 11 DEC 2015, DOI: 10.1002/dvdy.24368

  11. Does the cranial mesenchyme contribute to neural fold elevation during neurulation?

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 94, Issue 10, October 2012, Pages: 841–848, Irene E. Zohn and Anjali A. Sarkar

    Version of Record online : 3 SEP 2012, DOI: 10.1002/bdra.23073

  12. You have free access to this content
    Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation

    Journal of Anatomy

    Volume 204, Issue 6, June 2004, Pages: 487–499, Ileana Antonopoulou, Lampros A. Mavrogiannis, Andrew O. M. Wilkie and Gillian M. Morriss-Kay

    Version of Record online : 25 MAY 2004, DOI: 10.1111/j.0021-8782.2004.00304.x

  13. You have free access to this content
    The nucleotidase/phosphatase SAL1 is a negative regulator of drought tolerance in Arabidopsis

    The Plant Journal

    Volume 58, Issue 2, April 2009, Pages: 299–317, Pip B. Wilson, Gonzalo M. Estavillo, Katie J. Field, Wannarat Pornsiriwong, Adam J. Carroll, Katharine A. Howell, Nick S. Woo, Janice A. Lake, Steven M. Smith, A. Harvey Millar, Susanne Von Caemmerer and Barry J. Pogson

    Version of Record online : 28 JAN 2009, DOI: 10.1111/j.1365-313X.2008.03780.x

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    ASBMR 2010 Annual Meeting SU0001–SU0482

    Journal of Bone and Mineral Research

    Volume 25, Issue S1, 2010, Pages: S225–S362,

    Version of Record online : 16 JUN 2011, DOI: 10.1002/jbmr.5650251304

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    A mutation affecting ASCORBATE PEROXIDASE 2 gene expression reveals a link between responses to high light and drought tolerance

    Plant, Cell & Environment


    Version of Record online : 17 OCT 2005, DOI: 10.1111/j.1365-3040.2005.01419.x

  16. On the serial homology of the pectoral and pelvic girdles of tetrapods


    Volume 69, Issue 10, October 2015, Pages: 2543–2555, Karen E. Sears, Terence D. Capellini and Rui Diogo

    Version of Record online : 5 OCT 2015, DOI: 10.1111/evo.12773

  17. A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1–p13.3

    Clinical Genetics

    Volume 71, Issue 3, March 2007, Pages: 212–219, O Uyguner, H Kayserili, Y Li, B Karaman, G Nürnberg, HC Hennies, C Becker, P Nürnberg, S Başaran, MY Apak and B Wollnik

    Version of Record online : 12 JAN 2007, DOI: 10.1111/j.1399-0004.2007.00762.x

  18. Experimentally based sea urchin gene regulatory network and the causal explanation of developmental phenomenology

    Wiley Interdisciplinary Reviews: Systems Biology and Medicine

    Volume 1, Issue 2, September/October 2009, Pages: 237–246, Smadar Ben-Tabou de-Leon and Eric H. Davidson

    Version of Record online : 29 APR 2009, DOI: 10.1002/wsbm.24

  19. Mild nasal clefting may be predictive for ALX4 heterozygotes

    American Journal of Medical Genetics Part A

    Volume 164, Issue 8, August 2014, Pages: 2054–2058, Umut Altunoglu, Bilge Satkın, Zehra Oya Uyguner and Hülya Kayserili

    Version of Record online : 24 APR 2014, DOI: 10.1002/ajmg.a.36578

  20. You have free access to this content
    Pax6 regulates craniofacial form through its control of an essential cephalic ectodermal patterning center


    Volume 49, Issue 4, April 2011, Pages: 307–325, Claudia Compagnucci, Jennifer L. Fish, Manuela Schwark, Victor Tarabykin and Michael J. Depew

    Version of Record online : 14 APR 2011, DOI: 10.1002/dvg.20724