Search Results

There are 12584 results for: content related to: FGFR2 signaling and the pathogenesis of acne

  1. 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

  2. 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

  3. You have free access to this content
    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

  4. 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

  5. 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

  6. 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

  7. You have free access to this content
    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

  8. You have free access to this content
    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

  9. You have free access to this content
    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

    Version of Record online : 4 SEP 2008, DOI: 10.1002/dvdy.21648

  10. Reduces Bone Mass as in Human Apert Syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 5, May 2013, Pages: 983–992, Xia Zhou, Dongquan Pu, Ri Liu, Xiangjie Li, Xiujie Wen, Li Zhang, Lin Chen, Manjing Deng and Luchuan Liu

    Version of Record online : 13 MAR 2013, DOI: 10.1002/ajmg.a.35824

  11. You have free access to this content
    Brain phenotypes in two FGFR2 mouse models for Apert syndrome

    Developmental Dynamics

    Volume 239, Issue 3, March 2010, Pages: 987–997, Kristina Aldridge, Cheryl A. Hill, Jordan R. Austin, Christopher Percival, Neus Martinez-Abadias, Thomas Neuberger, Yingli Wang, Ethylin Wang Jabs and Joan T. Richtsmeier

    Version of Record online : 13 JAN 2010, DOI: 10.1002/dvdy.22218

  12. 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

    Version of Record online : 28 APR 2011, DOI: 10.1002/bdra.20811

  13. Genotype and clinical care correlations in craniosynostosis: Findings from a cohort of 630 Australian and New Zealand patients

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

    Volume 163, Issue 4, November 2013, Pages: 259–270, T. Roscioli, G. Elakis, T.C. Cox, D.J. Moon, H. Venselaar, A.M. Turner, T. Le, E. Hackett, E. Haan, A. Colley, D. Mowat, L. Worgan, E.P. Kirk, R. Sachdev, E. Thompson, M. Gabbett, J. McGaughran, K. Gibson, M. Gattas, M-L. Freckmann, J. Dixon, L. Hoefsloot, M. Field, A. Hackett, B. Kamien, M. Edwards, L.C. Adès, F.A. Collins, M.J. Wilson, R. Savarirayan, T.Y. Tan, D.J. Amor, G. McGIllivray, S.M. White, I.A. Glass, D.J. David, P.J. Anderson, M. Gianoutsos and M.F. Buckley

    Version of Record online : 11 OCT 2013, DOI: 10.1002/ajmg.c.31378

  14. Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing

    Human Mutation

    Volume 37, Issue 9, September 2016, Pages: 955–963, Christopher P. Barnett, Nathalie J. Nataren, Manuela Klingler-Hoffmann, Quenten Schwarz, Chan-Eng Chong, Young K. Lee, Damien L. Bruno, Jill Lipsett, Andrew J. McPhee, Andreas W. Schreiber, Jinghua Feng, Christopher N. Hahn and Hamish S. Scott

    Version of Record online : 11 JUL 2016, DOI: 10.1002/humu.23032

  15. Syndromic craniosynostosis: from history to hydrogen bonds

    Orthodontics & Craniofacial Research

    Volume 10, Issue 2, May 2007, Pages: 67–81, ML Cunningham, ML Seto, C Ratisoontorn, CL Heike and AV Hing

    Version of Record online : 5 JUN 2007, DOI: 10.1111/j.1601-6343.2007.00389.x

  16. You have free access to this content
    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

  17. You have free access to this content
    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

  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

    Version of Record online : 19 DEC 2013, DOI: 10.1002/dvdy.24099

  19. 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

  20. Acne-associated syndromes: models for better understanding of acne pathogenesis

    Journal of the European Academy of Dermatology and Venereology

    Volume 25, Issue 6, June 2011, Pages: 637–646, W Chen, B Obermayer-Pietsch, J-B Hong, BC Melnik, O Yamasaki, C Dessinioti, Q Ju, AI Liakou, S Al-Khuzaei, A Katsambas, J Ring and CC Zouboulis

    Version of Record online : 29 DEC 2010, DOI: 10.1111/j.1468-3083.2010.03937.x