Reactome | Mohammadi, M

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Mohammadi, M Show undefined attributes

dbId	111044
displayName	Mohammadi, M
firstname	Moosa
initial	M
modified	[InstanceEdit:1237406] D'Eustachio, P, 2011-03-30
publications	[LiteratureReference:2045057] Crystal structure of an angiogenesis inhibitor bound to the FGF receptor tyrosine kinase domain [LiteratureReference:191518] Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism [LiteratureReference:201396] Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors [LiteratureReference:190942] Identification of six novel autophosphorylation sites on fibroblast growth factor receptor 1 and elucidation of their importance in receptor activation and signal transduction [LiteratureReference:1295588] Point mutation in FGF receptor eliminates phosphatidylinositol hydrolysis without affecting mitogenesis [LiteratureReference:191025] A tyrosine-phosphorylated carboxy-terminal peptide of the fibroblast growth factor receptor (Flg) is a binding site for the SH2 domain of phospholipase C-gamma 1 [LiteratureReference:191519] Structural basis for fibroblast growth factor receptor activation [LiteratureReference:1307948] The FGF family: biology, pathophysiology and therapy [LiteratureReference:2059896] Structural basis for FGF receptor dimerization and activation [LiteratureReference:2011820] Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity [LiteratureReference:190251] Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family. [LiteratureReference:2029802] Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities [LiteratureReference:110026] The function of GRB2 in linking the insulin receptor to Ras signaling pathways. [LiteratureReference:1637891] Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes [LiteratureReference:1307951] Tissue-specific expression of betaKlotho and fibroblast growth factor (FGF) receptor isoforms determines metabolic activity of FGF19 and FGF21 [LiteratureReference:2033243] A molecular brake in the kinase hinge region regulates the activity of receptor tyrosine kinases [LiteratureReference:5577124] Crystal structure of a fibroblast growth factor homologous factor (FHF) defines a conserved surface on FHFs for binding and modulation of voltage-gated sodium channels [LiteratureReference:5654103] Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes [LiteratureReference:2033242] Loss-of-function fibroblast growth factor receptor-2 mutations in melanoma [LiteratureReference:1307940] Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members
schemaClass	Person
surname	Mohammadi

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