Analysis of mutations in fibroblast growth factor (FGF) and a pathogenic mutation in FGF receptor (FGFR) provides direct evidence for the symmetric two-end model for FGFR dimerization.

Analysis of mutations in fibroblast growth factor (FGF) and a pathogenic mutation in FGF receptor (FGFR) provides direct evidence for the symmetric two-end model for FGFR dimerization. Mol Cell Biol. 2005 Jan; 25(2):671-84.

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subject areas

Animals
Cells, Cultured
Dimerization
Fibroblast Growth Factor 10
Fibroblast Growth Factors
Heparin
Humans
Models, Molecular
Mutation
Protein Structure, Quaternary
Protein Structure, Secondary
Receptor, Fibroblast Growth Factor, Type 2
Receptors, Fibroblast Growth Factor
Signal Transduction
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Surface Plasmon Resonance

authors with profiles

Shaun K. Olsen