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There are 10213 results for: content related to: FGFs, their receptors, and human limb malformations: Clinical and molecular correlations

  1. Skeletal Dysplasias: Craniosynostosis Syndromes and Skeletal Dysplasias Caused by Mutations in Fibroblast Growth Factor Receptor Genes

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects, Second Edition

    Clair A. Francomano, Maximilian Muenke, Pages: 961–991, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221929.ch23(iv)

  2. 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

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

  3. 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

  4. 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

  5. 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

  6. 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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    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

  8. Clinical spectrum of fibroblast growth factor receptor mutations

    Human Mutation

    Volume 14, Issue 2, 1999, Pages: 115–125, M.R. Passos-Bueno, W.R. Wilcox, E.W. Jabs, A.L. Sertié, L.G. Alonso and H. Kitoh

    Article first published online : 28 JUL 1999, DOI: 10.1002/(SICI)1098-1004(1999)14:2<115::AID-HUMU3>3.0.CO;2-2

  9. 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

  10. Genotypic and phenotypic analyses of Korean patients with syndromic craniosynostosis

    Clinical Genetics

    Volume 76, Issue 3, September 2009, Pages: 287–291, JE Yu, S-Y Jeong, J-A Yang, MS Park, HJ Kim and SH Yoon

    Article first published online : 17 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01201.x

  11. FGFR2-Signaltransduktionswege in der Pathogenese der Akne

    JDDG: Journal der Deutschen Dermatologischen Gesellschaft

    Volume 6, Issue 9, September 2008, Page: no, Bodo Melnik and Gerd Schmitz

    Article first published online : 25 AUG 2008, DOI: 10.1111/j.1610-0387.2008.06822_supp.x

  12. Clinical dividends from the molecular genetic diagnosis of craniosynostosis

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 23, 1 December 2006, Pages: 2631–2639, Andrew O.M. Wilkie, Elena G. Bochukova, Ruth M. S. Hansen, Indira B. Taylor, Sahan V. Rannan-Eliya, Jo C. Byren, Steven A. Wall, Lina Ramos, Margarida Venâncio, Jane A. Hurst, Anthony W. O'Rourke, Louise J. Williams, Anneke Seller and Tracy Lester

    Article first published online : 12 JUL 2006, DOI: 10.1002/ajmg.a.31366

  13. Clinical dividends from the molecular genetic diagnosis of craniosynostosis

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 16, 15 August 2007, Pages: 1941–1949, Andrew O.M. Wilkie, Elena G. Bochukova, Ruth M. S. Hansen, Indira B. Taylor, Sahan V. Rannan-Eliya, Jo C. Byren, Steven A. Wall, Lina Ramos, Margarida Venâncio, Jane A. Hurst, Anthony W. O'Rourke, Louise J. Williams, Anneke Seller and Tracy Lester

    Article first published online : 9 JUL 2007, DOI: 10.1002/ajmg.a.31905

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

    International Journal of Cancer

    Danilo Ranieri, Francesca Belleudi, Alessandra Magenta and Maria Rosaria Torrisi

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

  15. FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome

    American Journal of Medical Genetics

    Volume 77, Issue 3, 18 May 1998, Pages: 219–224, Kathy Chun, Jacqueline Siegel-Bartelt, David Chitayat, John Phillips and Peter N. Ray

    Article first published online : 7 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19980518)77:3<219::AID-AJMG6>3.0.CO;2-K

  16. Mutation in the FGFR2 gene in a Taiwanese patient with Beare–Stevenson cutis gyrata syndrome

    Clinical Genetics

    Volume 61, Issue 3, March 2002, Pages: 218–221, T-J Wang, C-B Huang, F-J Tsai, J-Y Wu, R-B Lai and M Hsiao

    Article first published online : 8 MAY 2002, DOI: 10.1034/j.1399-0004.2002.610309.x

  17. Abnormal sterol metabolism in a patient with Antley-Bixler syndrome and ambiguous genitalia

    American Journal of Medical Genetics

    Volume 110, Issue 2, 15 June 2002, Pages: 95–102, Richard I. Kelley, Lisa E. Kratz, Rivka L. Glaser, Michael L. Netzloff, Linda Miller Wolf and Ethylin W. Jabs

    Article first published online : 25 APR 2002, DOI: 10.1002/ajmg.10510

  18. Emergence of FGFR family gene fusions as therapeutic targets in a wide spectrum of solid tumours

    The Journal of Pathology

    Volume 232, Issue 1, January 2014, Pages: 4–15, Brittany C Parker, Manon Engels, Matti Annala and Wei Zhang

    Article first published online : 6 DEC 2013, DOI: 10.1002/path.4297

  19. Novel FGFR2 deletion in a patient with Beare–Stevenson-like syndrome

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 8, August 2009, Pages: 1814–1817, Anne Slavotinek, Howard Crawford, Mahin Golabi, Cathy Tao, Hazel Perry, Sneha Oberoi, Karin Vargervik and Michael Friez

    Article first published online : 16 JUL 2009, DOI: 10.1002/ajmg.a.32947

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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