A novel tyrosine kinase inhibitor restores chondrocyte differentiation and promotes bone growth in a gain-of-function Fgfr3 mouse model

By Jonquoy Aurélie   Mugniery Emilie   Benoist-Lasselin Catherine   Kaci Nabil   Le Corre Laurent   Barbault Florent   Girard Anne-Lise   Le Merrer Yves   Busca Patricia   Schibler Laurent   Munnich Arnold   Legeai-Mallet Laurence  

Human Molecular Genetics, Vol. 21, Iss. 4, 2012-02 ,pp. : 841-851

Oxford University Press

Access to resources Recommend Favorite

Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA ( NTRK1 ) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor

By Mardy S.   Miura Y.   Endo F.   Matsuda I.   Indo Y.  

Human Molecular Genetics, Vol. 10, Iss. 3, 2001-02 ,pp. : 179-188

Oxford University Press

Access to resources Recommend Favorite

Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis

By Rannan-Eliya Sahan   Taylor Indira   Heer I.   Ouweland Ans   Wall Steven   Wilkie Andrew  

Human Genetics, Vol. 115, Iss. 3, 2004-08 ,pp. : 200-207

Springer Publishing Company

Access to resources Recommend Favorite

Mutations in TITF-1 are associated with benign hereditary chorea

By Joosse M.  

Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 971-979

Oxford University Press

Access to resources Recommend Favorite

A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors

By Iwata T.  

Human Molecular Genetics, Vol. 8, Iss. 1, 1999-01 ,pp. : 35-44

Oxford University Press

Access to resources Recommend Favorite