Increased EFG- and PDGF-receptor signaling by mutant FGF-receptor 2 contributes to osteoblast dysfunction in Apert craniosynostosis

By Miraoui Hichem   Ringe Jochen   Hupl Thomas   Marie Pierre J.  

Human Molecular Genetics, Vol. 19, Iss. 9, 2010-05 ,pp. : 1678-1689

Oxford University Press

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A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre–Chotzen syndrome

By Guenou Hind   Kaabeche Karim   Mée Sandrine Le   Marie Pierre J.  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1429-1439

Oxford University Press

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Defects in articular cartilage metabolism and early arthritis in fibroblast growth factor receptor 3 deficient mice

By Valverde-Franco G.   Binette J.S.   Li W.   Wang H.   Chai S.   Laflamme F.   Tran-Khanh N.   Quenneville E.   Meijers T.   Poole A.R.   Mort J.S.   Buschmann M.D.   Henderson J.E.  

Human Molecular Genetics, Vol. 15, Iss. 11, 2006-06 ,pp. : 1783-1792

Oxford University Press

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Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity

By Ibrahimi Omar A.  

Human Molecular Genetics, Vol. 13, Iss. 1, 2004-01 ,pp. : 69-78

Oxford University Press

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Natural mutations of the anti-Mllerian hormone type II receptor found in persistent Mllerian duct syndrome affect ligand binding, signal transduction and cellular transport

By Belville Corinne   Marchal Jean-Didier   Pennetier Sophie   Carmillo Paul   Masgrau Laura   Messika-Zeitoun Liza   Galey Julie   Machado Gabrielle   Treton Dominique   Gonzals Jacques   Picard Jean-Yves   Josso Nathalie   Cate Richard L.   di Clemente Nathalie  

Human Molecular Genetics, Vol. 18, Iss. 16, 2009-08 ,pp. : 3002-3013

Oxford University Press

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