FGFR2b mutant-binding FGFs

Stable Identifier
R-HSA-2065925
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
11121055 Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome

Yu, K, Herr, AB, Waksman, G, Ornitz, DM

Proc Natl Acad Sci U S A 2000
15282208 Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities

Ibrahimi, OA, Zhang, F, Eliseenkova, AV, Itoh, N, Linhardt, RJ, Mohammadi, M

Hum Mol Genet 2004
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