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There are 4387 results for: content related to: Brain phenotypes in two FGFR2 mouse models for Apert syndrome

  1. 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

    Article first published online : 12 MAR 2013, DOI: 10.1002/ajmg.a.35805

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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

    Article first published online : 12 MAY 2010, DOI: 10.1002/dvdy.22314

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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

    Article first published online : 17 JUN 2010, DOI: 10.1111/j.1469-7580.2010.01248.x

  4. 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

    Article first published online : 5 JAN 2012, DOI: 10.1002/jcb.23368

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    Evidence that Fgf10 contributes to the skeletal and visceral defects of an apert syndrome mouse model

    Developmental Dynamics

    Volume 238, Issue 2, February 2009, Pages: 376–385, Mohammad K. Hajihosseini, Raquel Duarte, Jean Pegrum, Anne Donjacour, Eva Lana-Elola, David P. Rice, James Sharpe and Clive Dickson

    Article first published online : 4 SEP 2008, DOI: 10.1002/dvdy.21648

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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

    Article first published online : 14 SEP 2010, DOI: 10.1002/dvdy.22414

  7. 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

    Article first published online : 13 MAR 2015, DOI: 10.1002/wdev.176

  8. 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

    Article first published online : 17 MAY 2012, DOI: 10.1002/jcp.24021

  9. Facial suture synostosis of newborn Fgfr1P250R/+ and Fgfr2S252W/+ mouse models of Pfeiffer and Apert syndromes

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 91, Issue 7, July 2011, Pages: 603–609, Roopa Purushothaman, Timothy C. Cox, A. Murat Muga and Michael L. Cunningham

    Article first published online : 28 APR 2011, DOI: 10.1002/bdra.20811

  10. Phosphorylation and lipid raft association of fibroblast growth factor receptor-2 in oligodendrocytes

    Glia

    Volume 57, Issue 9, July 2009, Pages: 935–946, M. R. Bryant, C. B. Marta, F. S. Kim and R. Bansal

    Article first published online : 2 DEC 2008, DOI: 10.1002/glia.20818

  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

    Article first published online : 28 NOV 2006, DOI: 10.1002/jcp.20880

  12. 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

    Article first published online : 27 AUG 2002, DOI: 10.1002/ajmg.10775

  13. 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

    Article first published online : 28 JUN 2006, DOI: 10.1111/j.1600-0625.2006.00450.x

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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

    Article first published online : 17 JUL 2009, DOI: 10.1002/dvdy.22032

  15. 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

    Article first published online : 17 SEP 2012, DOI: 10.1002/ajmg.a.35598

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    Signaling through FGF receptor-2 is required for lens cell survival and for withdrawal from the cell cycle during lens fiber cell differentiation

    Developmental Dynamics

    Volume 233, Issue 2, June 2005, Pages: 516–527, Claudia M. Garcia, Kai Yu, Haotian Zhao, Ruth Ashery-Padan, David M. Ornitz, Michael L. Robinson and David C. Beebe

    Article first published online : 18 MAR 2005, DOI: 10.1002/dvdy.20356

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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

    Article first published online : 7 FEB 2014, DOI: 10.1002/dvdy.24095

  18. You have full text access to this OnlineOpen article
    Soluble form of FGFR2 with S252W partially prevents craniosynostosis of the apert mouse model

    Developmental Dynamics

    Volume 243, Issue 4, April 2014, Pages: 560–567, Jumpei Morita, Masataka Nakamura, Yukiho Kobayashi, Chu-Xia Deng, Noriko Funato and Keiji Moriyama

    Article first published online : 19 DEC 2013, DOI: 10.1002/dvdy.24099

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    Fibroblast growth factor receptor 2 (Fgfr2) plays an important role in eyelid and skin formation and patterning

    Developmental Dynamics

    Volume 222, Issue 3, November 2001, Pages: 471–483, Cuiling Li, Huimin Guo, Xiaoling Xu, Wendy Weinberg and Chu-Xia Deng

    Article first published online : 2 OCT 2001, DOI: 10.1002/dvdy.1205

  20. A Novel FGFR2 Mutation in Tyrosine Kinase II Domain, L617F, in Crouzon Syndrome

    Journal of Cellular Biochemistry

    Volume 115, Issue 1, January 2014, Pages: 102–110, Ye-Jin Suh, Han-Sol Bae, Jin-Young Choi, Jong-Ho Lee, Myung-Jin Kim, Sukwha Kim, Hyun-Mo Ryoo and Seung-Hak Baek

    Article first published online : 14 NOV 2013, DOI: 10.1002/jcb.24637