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Fibroblast Growth Factor 8
Receptor, Fibroblast Growth Factor, Type 1
Receptor, Fibroblast Growth Factor, Type 2
Fibroblast Growth Factor 10
Fibroblast Growth Factor 1
Receptors, Fibroblast Growth Factor
Fibroblast Growth Factor 9
Fibroblast growth factor (FGF) homologous factors share structural but not functional homology with FGFs.
Insights into the molecular basis for fibroblast growth factor receptor autoinhibition and ligand-binding promiscuity.
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.
Structural basis for fibroblast growth factor receptor activation.
A protein canyon in the FGF-FGF receptor dimer selects from an ? la carte menu of heparan sulfate motifs.
Structural basis by which alternative splicing modulates the organizer activity of FGF8 in the brain.
Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family.
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members.
Homodimerization controls the fibroblast growth factor 9 subfamily's receptor binding and heparan sulfate-dependent diffusion in the extracellular matrix.
Plasticity in interactions of fibroblast growth factor 1 (FGF1) N terminus with FGF receptors underlies promiscuity of FGF1.
Fibroblast Growth Factor 4