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There are 45160 results for: content related to: Beyond the Closed Suture in Apert Syndrome Mouse Models: Evidence of Primary Effects of FGFR2 Signaling on Facial Shape at Birth

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    Beyond the closed suture in apert syndrome mouse models: Evidence of primary effects of FGFR2 signaling on facial shape at birth

    Developmental Dynamics

    Volume 239, Issue 11, November 2010, Pages: 3058–3071, Neus Martínez-Abadías, Christopher Percival, Kristina Aldridge, Cheryl A. Hill, Timothy Ryan, Satama Sirivunnabood, Yingli Wang, Ethylin Wang Jabs and Joan T. Richtsmeier

    Version of Record online : 14 SEP 2010, DOI: 10.1002/dvdy.22414

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    Tissue-specific responses to aberrant FGF signaling in complex head phenotypes

    Developmental Dynamics

    Volume 242, Issue 1, January 2013, Pages: 80–94, Neus Martínez-Abadías, Susan M. Motch, Talia L. Pankratz, Yingli Wang, Kristina Aldridge, Ethylin Wang Jabs and Joan T. Richtsmeier

    Version of Record online : 5 DEC 2012, DOI: 10.1002/dvdy.23903

  3. Postnatal brain and skull growth in an Apert syndrome mouse model

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 745–757, Cheryl A. Hill, Neus Martínez-Abadías, Susan M. Motch, Jordan R. Austin, Yingli Wang, Ethylin Wang Jabs, Joan T. Richtsmeier and Kristina Aldridge

    Version of Record online : 12 MAR 2013, DOI: 10.1002/ajmg.a.35805

  4. Fibroblast growth factor signaling in oligodendrocyte-lineage cells facilitates recovery of chronically demyelinated lesions but is redundant in acute lesions

    Glia

    Volume 63, Issue 10, October 2015, Pages: 1714–1728, Miki Furusho, Aude J. Roulois, Robin J. M. Franklin and Rashmi Bansal

    Version of Record online : 22 APR 2015, DOI: 10.1002/glia.22838

  5. Functional characterization of a novel FGFR2 mutation, E731K, in craniosynostosis

    Journal of Cellular Biochemistry

    Volume 113, Issue 2, February 2012, Pages: 457–464, Jounghyen Park, Ok-Jin Park, Won-Joon Yoon, Hyun-Jung Kim, Kang-Young Choi, Tae-Joon Cho and Hyun-Mo Ryoo

    Version of Record online : 5 JAN 2012, DOI: 10.1002/jcb.23368

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    The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling

    Developmental Dynamics

    Volume 239, Issue 6, June 2010, Pages: 1888–1900, S. Mai, K. Wei, A. Flenniken, S. L. Adamson, J. Rossant, J. E. Aubin and S.-G. Gong

    Version of Record online : 12 MAY 2010, DOI: 10.1002/dvdy.22314

  7. Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 4, April 2014, Pages: 250–259, Yann Heuzé, Neus Martínez-Abadías, Jennifer M. Stella, Eric Arnaud, Corinne Collet, Gemma García Fructuoso, Mariana Alamar, Lun-Jou Lo, Simeon A. Boyadjiev, Federico Di Rocco and Joan T. Richtsmeier

    Version of Record online : 27 FEB 2014, DOI: 10.1002/bdra.23228

  8. You have full text access to this OnlineOpen article
    The Fibroblast Growth Factor signaling pathway

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 4, Issue 3, May/June 2015, Pages: 215–266, David M. Ornitz and Nobuyuki Itoh

    Version of Record online : 13 MAR 2015, DOI: 10.1002/wdev.176

  9. Apert syndrome mutant FGFR2 and its soluble form reciprocally alter osteogenesis of primary calvarial osteoblasts

    Journal of Cellular Physiology

    Volume 227, Issue 9, September 2012, Pages: 3267–3277, Hiroyuki Suzuki, Naoto Suda, Momotoshi Shiga, Yukiho Kobayashi, Masataka Nakamura, Sachiko Iseki and Keiji Moriyama

    Version of Record online : 17 MAY 2012, DOI: 10.1002/jcp.24021

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    Embryonic craniofacial bone volume and bone mineral density in Fgfr2+/P253R and nonmutant mice

    Developmental Dynamics

    Volume 243, Issue 4, April 2014, Pages: 541–551, Christopher J. Percival, Yuan Huang, Ethylin Wang Jabs, Runze Li and Joan T. Richtsmeier

    Version of Record online : 7 FEB 2014, DOI: 10.1002/dvdy.24095

  11. Differential signal transduction of alternatively spliced FGFR2 variants expressed in human mammary epithelial cells

    Journal of Cellular Physiology

    Volume 210, Issue 3, March 2007, Pages: 720–731, Allison B. Moffa and Stephen P. Ethier

    Version of Record online : 28 NOV 2006, DOI: 10.1002/jcp.20880

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    Dynamic morphological changes in the skulls of mice mimicking human Apert syndrome resulting from gain-of-function mutation of FGFR2 (P253R)

    Journal of Anatomy

    Volume 217, Issue 2, August 2010, Pages: 97–105, Xiaolan Du, Tujun Weng, Qidi Sun, Nan Su, Zhi Chen, Huabing Qi, Ming Jin, Liangjun Yin, Qifen He and Lin Chen

    Version of Record online : 17 JUN 2010, DOI: 10.1111/j.1469-7580.2010.01248.x

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    Tissue-specific roles of FGF signaling in external genitalia development

    Developmental Dynamics

    Volume 244, Issue 6, June 2015, Pages: 759–773, Masayo Harada, Akiko Omori, Chiaki Nakahara, Naomi Nakagata, Keiichi Akita and Gen Yamada

    Version of Record online : 27 MAY 2015, DOI: 10.1002/dvdy.24277

  14. FGFs, their receptors, and human limb malformations: Clinical and molecular correlations

    American Journal of Medical Genetics

    Volume 112, Issue 3, 15 October 2002, Pages: 266–278, Andrew O.M. Wilkie, Susannah J. Patey, Shih-hsin Kan, Ans M.W. van den Ouweland and Ben C.J. Hamel

    Version of Record online : 27 AUG 2002, DOI: 10.1002/ajmg.10775

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    miR-223 Regulates Adipogenic and Osteogenic Differentiation of Mesenchymal Stem Cells Through a C/EBPs/miR-223/FGFR2 Regulatory Feedback Loop

    STEM CELLS

    Volume 33, Issue 5, May 2015, Pages: 1589–1600, Xiaohui Guan, Yifei Gao, Jie Zhou, Jun Wang, Fang Zheng, Fei Guo, Ailing Chang, Xiaoxia Li and Baoli Wang

    Version of Record online : 23 APR 2015, DOI: 10.1002/stem.1947

  16. The expression of keratinocyte growth factor receptor (FGFR2-IIIb) correlates with the high proliferative rate of HaCaT keratinocytes

    Experimental Dermatology

    Volume 15, Issue 8, August 2006, Pages: 596–605, Nikoletta Nagy, Zsuzsanna Bata-Csörgő, Norbert Kopasz, Csilla Szeg, Andor Pivarcsi, Andrea Koreck, Attila Dobozy, Lajos Kemény and Márta Széll

    Version of Record online : 28 JUN 2006, DOI: 10.1111/j.1600-0625.2006.00450.x

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    HPV16 E5 expression induces switching from FGFR2b to FGFR2c and epithelial-mesenchymal transition

    International Journal of Cancer

    Volume 137, Issue 1, 1 July 2015, Pages: 61–72, Danilo Ranieri, Francesca Belleudi, Alessandra Magenta and Maria Rosaria Torrisi

    Version of Record online : 13 DEC 2014, DOI: 10.1002/ijc.29373

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    Conditional gene inactivation reveals roles for Fgf10 and Fgfr2 in establishing a normal pattern of epithelial branching in the mouse lung

    Developmental Dynamics

    Volume 238, Issue 8, August 2009, Pages: 1999–2013, Lisa L. Abler, Suzanne L. Mansour and Xin Sun

    Version of Record online : 17 JUL 2009, DOI: 10.1002/dvdy.22032

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    Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

    Journal of Anatomy

    Volume 207, Issue 5, November 2005, Pages: 637–653, Gillian M. Morriss-Kay and Andrew O. M. Wilkie

    Version of Record online : 2 NOV 2005, DOI: 10.1111/j.1469-7580.2005.00475.x

  20. Central nervous system malformations and deformations in FGFR2-related craniosynostosis

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2797–2806, Roman Hossein Khonsari, Anne-Lise Delezoide, Wenfei Kang, Jean M. Hébert, Bettina Bessières, Valérie Bodiguel, Catherine Collet, Laurence Legeai-Mallet, Paul T. Sharpe and Catherine Fallet-Bianco

    Version of Record online : 17 SEP 2012, DOI: 10.1002/ajmg.a.35598