The Thanatophoric Dysplasia Type II Mutation Hampers Complete Maturation of Fibroblast Growth Factor Receptor 3 (FGFR3), Which Activates Signal Transducer and Activator of Transcription 1 (STAT1) from the Endoplasmic Reticulum
Open Access
- 1 May 2003
- journal article
- Published by Elsevier
- Vol. 278 (19) , 17344-17349
- https://doi.org/10.1074/jbc.m212710200
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- FRS2α attenuates FGF receptor signaling by Grb2- mediated recruitment of the ubiquitin ligase CblProceedings of the National Academy of Sciences, 2002
- A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryosHuman Molecular Genetics, 2000
- Fibroblast Growth Factors as Multifunctional Signaling FactorsPublished by Elsevier ,1998
- FGFR activation in skeletal disorders: Too much of a good thingTrends in Genetics, 1997
- Profound Ligand-Independent Kinase Activation of Fibroblast Growth Factor Receptor 3 by the Activation Loop Mutation Responsible for a Lethal Skeletal Dysplasia, Thanatophoric Dysplasia Type IIMolecular and Cellular Biology, 1996
- Identification of Six Novel Autophosphorylation Sites on Fibroblast Growth Factor Receptor 1 and Elucidation of Their Importance in Receptor Activation and Signal TransductionMolecular and Cellular Biology, 1996
- Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3Nature Genetics, 1995
- Heparin-induced oligomerization of FGF molecules is responsible for FGF receptor dimerization, activation, and cell proliferationCell, 1994
- The Fgf Family of Growth Factors and OncogenesPublished by Elsevier ,1992
- Signal transduction by receptors with tyrosine kinase activityPublished by Elsevier ,1990