Gene interactions and pathways from curated databases and text-mining

◀ Back to FGFR3

FGF10 — FGFR3

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Wang et al., Growth Factors 2000 : The biological activities of fibroblast growth factors ( FGF ) are mediated by specific cell membrane receptors ( FGFR ), which have three immunoglobulin-like IgG domains in the extracellular region
Pellegrini et al., Curr Opin Struct Biol 2001 : Fibroblast growth factors ( FGFs ) are among the best studied heparin binding proteins, and heparan sulfate proteoglycans regulate FGF signalling by direct molecular association with FGF and its tyrosine kinase receptor, FGFR
Anderson et al., J Neurochem 2005 : Dendrimeric FRM peptide was 125-fold more active and stimulated FGFR activation, FGFR dependent and FGF-mimetic neurite outgrowth and cell survival ( but not proliferation )
Buratini et al., Biol Reprod 2007 : Whereas many FGFs activate several FGF receptors, FGF7 and FGF10 primarily activate only one, FGFR2B
Li et al., Mol Cell Endocrinol 2012 : In hepatocyte, FGF-21 up-regulation reduced HMGR and PEPCK mRNA expression and increased ß-klotho, FGFR4 and LDLr expression ( p < 0.05 ), whereas down-regulation had the opposite effects
Ahmad et al., Biochim Biophys Acta 2012 (Cell Transformation, Neoplastic...) : FGF signalling mediated by FGFR follows a classic receptor tyrosine kinase signalling pathway and its deregulation at various points of its cascade could result in malignancy
Itoh et al., Development 1996 : These results suggest that the FGFR mediated FGF signaling ( 1 ) blocks terminal differentiation of myogenic cells within the somite and ( 2 ) sustains myoblast migration to limb buds from the somite, and that ( 3 ) down-regulation of FGFRs or FGFR signaling is involved in mechanisms triggering terminal differentiation of the limb muscle mass during avian embryogenesis
Santos-Ocampo et al., J Biol Chem 1996 : Significantly, FGF-9 also binds to and activates the `` b '' splice form of FGFR3 , thus becoming the first FGF ligand besides FGF-1 to activate this highly specific member of the FGF receptor family
McKeehan et al., Prog Nucleic Acid Res Mol Biol 1998 : Divalent cations cooperate with the FGFRHS to conformationally restrict FGFRTK trans-phosphorylation, which causes depression of kinase activity and facilitates appropriate activation of the FGFR complex by FGF