Literature DB >> 11274381

Uncoupling fibroblast growth factor receptor 2 ligand binding specificity leads to Apert syndrome-like phenotypes.

K Yu1, D M Ornitz.   

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Year:  2001        PMID： 11274381      PMCID： PMC33332          DOI： 10.1073/pnas.081082498

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  33 in total

1.  Characterization of recombinant human fibroblast growth factor (FGF)-10 reveals functional similarities with keratinocyte growth factor (FGF-7).

Authors:  M Igarashi; P W Finch; S A Aaronson
Journal:  J Biol Chem       Date:  1998-05-22       Impact factor: 5.157

2.  Receptor specificity of the fibroblast growth factor family.

Authors:  D M Ornitz; J Xu; J S Colvin; D G McEwen; C A MacArthur; F Coulier; G Gao; M Goldfarb
Journal:  J Biol Chem       Date:  1996-06-21       Impact factor: 5.157

Review 3.  The heparan sulfate-fibroblast growth factor family: diversity of structure and function.

Authors:  W L McKeehan; F Wang; M Kan
Journal:  Prog Nucleic Acid Res Mol Biol       Date:  1998

4.  Targeted disruption of fibroblast growth factor (FGF) receptor 2 suggests a role for FGF signaling in pregastrulation mammalian development.

Authors:  E Arman; R Haffner-Krausz; Y Chen; J K Heath; P Lonai
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

Review 5.  Functions of fibroblast growth factors and their receptors.

Authors:  A O Wilkie; G M Morriss-Kay; E Y Jones; J K Heath
Journal:  Curr Biol       Date:  1995-05-01       Impact factor: 10.834

Review 6.  Fibroblast-growth-factor receptor mutations in human skeletal disorders.

Authors:  M Muenke; U Schell
Journal:  Trends Genet       Date:  1995-08       Impact factor: 11.639

7.  Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras.

Authors:  B D Galvin; K C Hart; A N Meyer; M K Webster; D J Donoghue
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-23       Impact factor: 11.205

8.  Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

Authors:  A O Wilkie; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland
Journal:  Nat Genet       Date:  1995-02       Impact factor: 38.330

9.  An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.

Authors:  L De Moerlooze; B Spencer-Dene; J M Revest; M Hajihosseini; I Rosewell; C Dickson
Journal:  Development       Date:  2000-02       Impact factor: 6.868

10.  Fibroblast growth factor receptor 2 (FGFR2)-mediated reciprocal regulation loop between FGF8 and FGF10 is essential for limb induction.

Authors:  X Xu; M Weinstein; C Li; M Naski; R I Cohen; D M Ornitz; P Leder; C Deng
Journal:  Development       Date:  1998-02       Impact factor: 6.868
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  18 in total

1.  Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family.

Authors:  Xiuqin Zhang; Omar A Ibrahimi; Shaun K Olsen; Hisashi Umemori; Moosa Mohammadi; David M Ornitz
Journal:  J Biol Chem       Date:  2006-04-04       Impact factor: 5.157

2.  Mouse models of Apert syndrome.

Authors:  Greg Holmes
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

Review 3.  Signaling networks in joint development.

Authors:  Joanna E Salva; Amy E Merrill
Journal:  Dev Dyn       Date:  2016-12-29       Impact factor: 3.780

Review 4.  FGF signaling in the developing endochondral skeleton.

Authors:  David M Ornitz
Journal:  Cytokine Growth Factor Rev       Date:  2005-04-01       Impact factor: 7.638

5.  Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia.

Authors:  Anne Goriely; Gilean A T McVean; Ans M M van Pelt; Anthony W O'Rourke; Steven A Wall; Dirk G de Rooij; Andrew O M Wilkie
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-19       Impact factor: 11.205

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

Authors:  Neus Martínez-Abadías; Christopher Percival; Kristina Aldridge; Cheryl A Hill; Timothy Ryan; Satama Sirivunnabood; Yingli Wang; Ethylin Wang Jabs; Joan T Richtsmeier
Journal:  Dev Dyn       Date:  2010-11       Impact factor: 3.780

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

Authors:  Cheryl A Hill; Neus Martínez-Abadías; Susan M Motch; Jordan R Austin; Yingli Wang; Ethylin Wang Jabs; Joan T Richtsmeier; Kristina Aldridge
Journal:  Am J Med Genet A       Date:  2013-03-12       Impact factor: 2.802

Review 8.  Molecular mechanisms of fibroblast growth factor signaling in physiology and pathology.

Authors:  Artur A Belov; Moosa Mohammadi
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-06-01       Impact factor: 10.005

9.  Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome.

Authors:  Caterina Tiozzo; Stijn De Langhe; Gianni Carraro; Denise Al Alam; Andre Nagy; Clarence Wigfall; Mohammad K Hajihosseini; David Warburton; Parviz Minoo; Saverio Bellusci
Journal:  Pediatr Res       Date:  2009-10       Impact factor: 3.756

Review 10.  A Genetic-Pathophysiological Framework for Craniosynostosis.

Authors:  Stephen R F Twigg; Andrew O M Wilkie
Journal:  Am J Hum Genet       Date:  2015-09-03       Impact factor: 11.025
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