The Muenke syndrome mutation (FgfR3P244R) causes cranial base shortening associated with growth plate dysfunction and premature perichondrial ossification in murine basicranial synchondroses-Reference-Cited by-同舟云学术

The Muenke syndrome mutation (FgfR3P244R) causes cranial base shortening associated with growth plate dysfunction and premature perichondrial ossification in murine basicranial synchondroses

Published:2011-10-05 Issue:11 Volume:240 Page:2584-2596
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Dev. Dyn.

Author:

Laurita Jason,Koyama Eiki,Chin Bianca,Taylor Jesse A.,Lakin Gregory E.,Hankenson Kurt D.,Bartlett Scott P.,Nah Hyun-Duck

Publisher

Wiley

Subject

Developmental Biology

Reference44 articles.

1. Achondroplasia is defined by recurrent G380R mutations of FGFR3;Bellus;Am J Hum Genet,1995a

2. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia;Bellus;Nat Genet,1995b

3. A Ser(365)→Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates Ihh/PTHrP signals and causes severe achondroplasia;Chen;Hum Mol Genet,2001

4. Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3;Colvin;Nat Genet,1996

5. Snail1 is a transcriptional effector of FGFR3 signaling during chondrogenesis and achondroplasias;de Frutos;Dev Cell,2007

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