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There are 9715 results for: content related to: The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling

  1. 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

  2. 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

  3. 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

  4. Screening of patients with craniosynostosis: Molecular strategy

    American Journal of Medical Genetics Part A

    Volume 120A, Issue 4, 1 August 2003, Pages: 470–473, Kathy Chun, Ahmad S. Teebi, Cyrus Azimi, Leslie Steele and Peter N. Ray

    Article first published online : 17 JUL 2003, DOI: 10.1002/ajmg.a.20258

  5. You have free access to this content
    Fibroblast growth factor 23 reduces expression of type IIa Na+/Pi co-transporter by signaling through a receptor functionally distinct from the known FGFRs in opossum kidney cells

    Genes to Cells

    Volume 10, Issue 5, May 2005, Pages: 489–502, Xiaomei Yan, Hideyuki Yokote, Xuefeng Jing, Li Yao, Takahiro Sawada, Yueqiang Zhang, Sitai Liang and Kazushige Sakaguchi

    Article first published online : 31 MAR 2005, DOI: 10.1111/j.1365-2443.2005.00853.x

  6. You have full text access to this OnlineOpen article
    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

    Article first published online : 13 DEC 2014, DOI: 10.1002/ijc.29373

  7. Distinct craniofacial-skeletal-dermatological dysplasia in a patient with W290C mutation in FGFR2

    American Journal of Medical Genetics

    Volume 113, Issue 1, 15 November 2002, Pages: 4–8, Vorasuk Shotelersuk, Chupong Ittiwut, Sumarlee Srivuthana, Charan Mahatumarat, Sukalaya Lerdlum and Suthipong Wacharasindhu

    Article first published online : 10 MAY 2002, DOI: 10.1002/ajmg.10449

  8. You have free access to this content
    Re-programming of expression of the KGFR and bek variants of fibroblast growth factor receptor 2 during limb regeneration in newts (Notophthalmus viridescens)

    Developmental Dynamics

    Volume 202, Issue 4, April 1995, Pages: 378–387, Matthew L. Poulin and Dr. Ing-Ming Chiu

    Article first published online : 3 FEB 2005, DOI: 10.1002/aja.1002020407

  9. Down-regulation of (IIIb) and (IIIc) isoforms of fibroblast growth factor receptor 2 (FGFR2) is associated with malignant progression in human prostate

    The Prostate

    Volume 52, Issue 3, 1 August 2002, Pages: 245–252, Benyoussef Naimi, Alain Latil, Georges Fournier, Philippe Mangin, Olivier Cussenot and Philippe Berthon

    Article first published online : 17 JUN 2002, DOI: 10.1002/pros.10104

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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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    Mutation analysis of Crouzon syndrome in Taiwanese patients

    Journal of Clinical Laboratory Analysis

    Volume 20, Issue 1, 2006, Pages: 23–26, Chin-Ping Chang, Lei Wan, Chang-Hai Tsai, Cheng-Chun Lee and Fuu-Jen Tsai

    Article first published online : 8 FEB 2006, DOI: 10.1002/jcla.20096

  12. 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

  13. Heparin Modulates the Mitogenic Activity of Fibroblast Growth Factor by Inducing Dimerization of its Receptor. A 3D View by Using NMR

    ChemBioChem

    Volume 14, Issue 14, September 23, 2013, Pages: 1732–1744, Dr. Lidia Nieto, Dr. Ángeles Canales, Dr. Israel S. Fernández, Dr. Elena Santillana, Dr. Rocío González-Corrochano, Dr. Mariano Redondo-Horcajo, Prof. F. Javier Cañada, Dr. Pedro Nieto, Prof. Manuel Martín-Lomas, Prof. Guillermo Giménez-Gallego and Prof. Jesús Jiménez-Barbero

    Article first published online : 12 AUG 2013, DOI: 10.1002/cbic.201300313

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    CCN2/CTGF binds to fibroblast growth factor receptor 2 and modulates its signaling

    FEBS Letters

    Volume 586, Issue 24, December 14, 2012, Pages: 4270–4275, Eriko Aoyama , Satoshi Kubota and Masaharu Takigawa

    Article first published online : 6 NOV 2012, DOI: 10.1016/j.febslet.2012.10.038

  15. Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses

    American Journal of Medical Genetics

    Volume 78, Issue 3, 7 July 1998, Pages: 237–241, Maria Rita Passos-Bueno, Andréa L. Sertié, Antonio Richieri-Costa, Luís G. Alonso, Mayana Zatz, Nivaldo Alonso, Décio Brunoni and Sandra F.M. Ribeiro

    Article first published online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980707)78:3<237::AID-AJMG5>3.0.CO;2-M

  16. Genetic Etiologies of Craniosynostosis

    Understanding Craniofacial Anomalies

    Mark P. Mooney, Michael I. Siegel, Pages: 125–146, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221953.ch6

  17. Epithelial–mesenchymal transition in keloid tissues and TGF-β1–induced hair follicle outer root sheath keratinocytes

    Wound Repair and Regeneration

    Volume 23, Issue 4, July/August 2015, Pages: 601–610, Li Yan, Rui Cao, Lianzhao Wang, Yuanbo Liu, Bo Pan, Yanhua Yin, Xiaoyan Lv, Qiang Zhuang, Xuejian Sun and Ran Xiao

    Article first published online : 14 JUL 2015, DOI: 10.1111/wrr.12320

  18. 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

  19. 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

    Article first published online : 22 APR 2015, DOI: 10.1002/glia.22838

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    Fibroblast growth factor receptor-2 mutation analysis in human prostate cancer

    BJU International

    Volume 86, Issue 6, October 2000, Pages: 681–685, P. Mehta, C.N. Robson, D.E. Neal and H.Y. Leung

    Article first published online : 24 DEC 2001, DOI: 10.1046/j.1464-410x.2000.00893.x