Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice

By Li C-L.   Deng C-X.   Iwata T.   Francomano C.A.  

Human Molecular Genetics, Vol. 10, Iss. 12, 2001-06 ,pp. : 1255-1264

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

A Ser 365 →Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates Ihh/PTHrP signals and causes severe achondroplasia

By Chen L.   Li C.   Qiao W.   Xu X.   Deng C.  

Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 457-465

Oxford University Press

Access to resources Recommend Favorite

Activating mutations of the tyrosine kinase receptor FGFR3 are associated with benign skin tumors in mice and humans

By Logié Armelle  

Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1153-1160

Oxford University Press

Access to resources Recommend Favorite

Restrained chondrocyte proliferation and maturation with abnormal growth plate vascularization and ossification in human FGFR-3 G380R transgenic mice

By Segev Orit  

Human Molecular Genetics, Vol. 9, Iss. 2, 2000-01 ,pp. : 249-258

Oxford University Press

Access to resources Recommend Favorite