A multifunctional docking site mediates signaling and transformation by the hepatocyte growth factor/scatter factor receptor family
about
Ligand-regulated binding of FAP68 to the hepatocyte growth factor receptorUse of signal specific receptor tyrosine kinase oncoproteins reveals that pathways downstream from Grb2 or Shc are sufficient for cell transformation and metastasisA quantitative protein interaction network for the ErbB receptors using protein microarraysInterplay between scatter factor receptors and B plexins controls invasive growthInteraction of phospholipase C-gamma1 with villin regulates epithelial cell migrationStructural characterization of autoinhibited c-Met kinase produced by coexpression in bacteria with phosphatase.Identification of six novel autophosphorylation sites on fibroblast growth factor receptor 1 and elucidation of their importance in receptor activation and signal transductionStructural determinants of the interaction between the erbB2 receptor and the Src homology 2 domain of Grb7The evolutionarily conserved EBR module of RALT/MIG6 mediates suppression of the EGFR catalytic activityConstruction of an SH2 domain-binding site with mixed specificityA family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptorThe cytoplasmic tyrosine kinase FER is associated with the catenin-like substrate pp120 and is activated by growth factors.HGF receptor associates with the anti-apoptotic protein BAG-1 and prevents cell deathHepatocyte growth factor receptor tyrosine kinase met is a substrate of the receptor protein-tyrosine phosphatase DEP-1The beta-subunit of the hepatocyte growth factor/scatter factor (HGF/SF) receptor phosphorylates and associates with CrkII: expression of CrkII enhances HGF/SF-induced mitogenesisAb-induced ectodomain shedding mediates hepatocyte growth factor receptor down-regulation and hampers biological activityMet-HGF/SF signal transduction induces mimp, a novel mitochondrial carrier homologue, which leads to mitochondrial depolarizationThe Gab1 PH domain is required for localization of Gab1 at sites of cell-cell contact and epithelial morphogenesis downstream from the met receptor tyrosine kinaseSTK/RON receptor tyrosine kinase mediates both apoptotic and growth signals via the multifunctional docking site conserved among the HGF receptor familyRON is a heterodimeric tyrosine kinase receptor activated by the HGF homologue MSPWiskott-Aldrich syndrome protein is associated with the adapter protein Grb2 and the epidermal growth factor receptor in living cellsThe MET axis as a therapeutic target.An overview of the c-MET signaling pathwayCrystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-Met and its complex with the microbial alkaloid K-252aScatter factor/hepatocyte growth factor in brain tumor growth and angiogenesisEssential role of Gab1 for signaling by the c-Met receptor in vivoBiomarker development in MET-targeted therapyProstate cancer metastasis: roles of recruitment and reprogramming, cell signal network and three-dimensional growth characteristicsc-Met as a Target for Personalized TherapyPathogenesis of RON receptor tyrosine kinase in cancer cells: activation mechanism, functional crosstalk, and signaling addictionSAMe and HuR in liver physiology: usefulness of stem cells in hepatic differentiation researchTargeting the epithelial to mesenchymal transition in glioblastoma: the emerging role of MET signalingNormal morphogenesis of epithelial tissues and progression of epithelial tumors.IKKβ acts as a tumor suppressor in cancer-associated fibroblasts during intestinal tumorigenesis.Evidence for SH2 domain-containing 5'-inositol phosphatase-2 (SHIP2) contributing to a lymphatic dysfunctionBiology of MET: a double life between normal tissue repair and tumor progressionSustained recruitment of phospholipase C-gamma to Gab1 is required for HGF-induced branching tubulogenesisMet receptor tyrosine kinase: enhanced signaling through adapter proteinsThe SH2 inositol 5-phosphatase Ship1 is recruited in an SH2-dependent manner to the erythropoietin receptorHGF/SF-met signaling in the control of branching morphogenesis and invasion
P2860
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P2860
A multifunctional docking site mediates signaling and transformation by the hepatocyte growth factor/scatter factor receptor family
description
1994 nî lūn-bûn
@nan
1994 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
A multifunctional docking site ...... scatter factor receptor family
@ast
A multifunctional docking site ...... scatter factor receptor family
@en
A multifunctional docking site ...... scatter factor receptor family
@nl
type
label
A multifunctional docking site ...... scatter factor receptor family
@ast
A multifunctional docking site ...... scatter factor receptor family
@en
A multifunctional docking site ...... scatter factor receptor family
@nl
prefLabel
A multifunctional docking site ...... scatter factor receptor family
@ast
A multifunctional docking site ...... scatter factor receptor family
@en
A multifunctional docking site ...... scatter factor receptor family
@nl
P2093
P3181
P1433
P1476
A multifunctional docking site ...... scatter factor receptor family
@en
P2093
A Bardelli
A Graziani
C Ponzetto
G Panayotou
P M Comoglio
P dalla Zonca
S Giordano
P304
P3181
P356
10.1016/0092-8674(94)90318-2
P407
P577
1994-04-22T00:00:00Z