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169 related items for PubMed ID: 9365521

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Receptor chimeras indicate that the met tyrosine kinase mediates the motility and morphogenic responses of hepatocyte growth/scatter factor.
    Zhu H, Naujokas MA, Park M.
    Cell Growth Differ; 1994 Apr; 5(4):359-66. PubMed ID: 8043510
    [Abstract] [Full Text] [Related]

  • 3. Inhibition of junction assembly in cultured epithelial cells by hepatocyte growth factor/scatter factor is concomitant with increased stability and altered phosphorylation of the soluble junctional molecules.
    Pasdar M, Li Z, Marreli M, Nguyen BT, Park M, Wong K.
    Cell Growth Differ; 1997 Apr; 8(4):451-62. PubMed ID: 9101091
    [Abstract] [Full Text] [Related]

  • 4. Hepatocyte growth factor-induced scatter of Madin-Darby canine kidney cells requires phosphatidylinositol 3-kinase.
    Royal I, Park M.
    J Biol Chem; 1995 Nov 17; 270(46):27780-7. PubMed ID: 7499247
    [Abstract] [Full Text] [Related]

  • 5. Branching tubulogenesis but not scatter of madin-darby canine kidney cells requires a functional Grb2 binding site in the Met receptor tyrosine kinase.
    Fournier TM, Kamikura D, Teng K, Park M.
    J Biol Chem; 1996 Sep 06; 271(36):22211-7. PubMed ID: 8703035
    [Abstract] [Full Text] [Related]

  • 6. Regulation of the urokinase-type plasminogen activator gene by the oncogene Tpr-Met involves GRB2.
    Besser D, Bardelli A, Didichenko S, Thelen M, Comoglio PM, Ponzetto C, Nagamine Y.
    Oncogene; 1997 Feb 13; 14(6):705-11. PubMed ID: 9038378
    [Abstract] [Full Text] [Related]

  • 7. Tyrosine 1356 in the carboxyl-terminal tail of the HGF/SF receptor is essential for the transduction of signals for cell motility and morphogenesis.
    Zhu H, Naujokas MA, Fixman ED, Torossian K, Park M.
    J Biol Chem; 1994 Nov 25; 269(47):29943-8. PubMed ID: 7961992
    [Abstract] [Full Text] [Related]

  • 8. The cell dissociation and motility triggered by scatter factor/hepatocyte growth factor are mediated through the cytoplasmic domain of the c-Met receptor.
    Komada M, Kitamura N.
    Oncogene; 1993 Sep 25; 8(9):2381-90. PubMed ID: 7689722
    [Abstract] [Full Text] [Related]

  • 9. Efficient cell transformation by the Tpr-Met oncoprotein is dependent upon tyrosine 489 in the carboxy-terminus.
    Fixman ED, Naujokas MA, Rodrigues GA, Moran MF, Park M.
    Oncogene; 1995 Jan 19; 10(2):237-49. PubMed ID: 7838524
    [Abstract] [Full Text] [Related]

  • 10. Concomitant activation of pathways downstream of Grb2 and PI 3-kinase is required for MET-mediated metastasis.
    Bardelli A, Basile ML, Audero E, Giordano S, Wennström S, Ménard S, Comoglio PM, Ponzetto C.
    Oncogene; 1999 Feb 04; 18(5):1139-46. PubMed ID: 10022119
    [Abstract] [Full Text] [Related]

  • 11. Mechanisms of hepatocyte growth factor-induced retinal endothelial cell migration and growth.
    Cai W, Rook SL, Jiang ZY, Takahara N, Aiello LP.
    Invest Ophthalmol Vis Sci; 2000 Jun 04; 41(7):1885-93. PubMed ID: 10845613
    [Abstract] [Full Text] [Related]

  • 12. Hepatocyte growth factor exerts multiple biological functions on bovine mammary epithelial cells.
    Accornero P, Martignani E, Macchi E, Baratta M.
    J Dairy Sci; 2007 Sep 04; 90(9):4289-96. PubMed ID: 17699048
    [Abstract] [Full Text] [Related]

  • 13. Hepatocyte growth factor stimulates cell motility in cultures of the striatal progenitor cells ST14A.
    Cacci E, Salani M, Anastasi S, Perroteau I, Poiana G, Biagioni S, Augusti-Tocco G.
    J Neurosci Res; 2003 Dec 01; 74(5):760-8. PubMed ID: 14635227
    [Abstract] [Full Text] [Related]

  • 14. Structure, biosynthesis and biochemical properties of the HGF receptor in normal and malignant cells.
    Comoglio PM.
    EXS; 1993 Dec 01; 65():131-65. PubMed ID: 8380735
    [Abstract] [Full Text] [Related]

  • 15. MUC20 suppresses the hepatocyte growth factor-induced Grb2-Ras pathway by binding to a multifunctional docking site of met.
    Higuchi T, Orita T, Katsuya K, Yamasaki Y, Akiyama K, Li H, Yamamoto T, Saito Y, Nakamura M.
    Mol Cell Biol; 2004 Sep 01; 24(17):7456-68. PubMed ID: 15314156
    [Abstract] [Full Text] [Related]

  • 16. Sustained recruitment of phospholipase C-gamma to Gab1 is required for HGF-induced branching tubulogenesis.
    Gual P, Giordano S, Williams TA, Rocchi S, Van Obberghen E, Comoglio PM.
    Oncogene; 2000 Mar 16; 19(12):1509-18. PubMed ID: 10734310
    [Abstract] [Full Text] [Related]

  • 17. Adaptor molecule Crk is required for sustained phosphorylation of Grb2-associated binder 1 and hepatocyte growth factor-induced cell motility of human synovial sarcoma cell lines.
    Watanabe T, Tsuda M, Makino Y, Ichihara S, Sawa H, Minami A, Mochizuki N, Nagashima K, Tanaka S.
    Mol Cancer Res; 2006 Jul 16; 4(7):499-510. PubMed ID: 16849525
    [Abstract] [Full Text] [Related]

  • 18. HGF controls branched morphogenesis in tubular glands.
    Maffè A, Comoglio PM.
    Eur J Morphol; 1998 Aug 16; 36 Suppl():74-81. PubMed ID: 9825897
    [Abstract] [Full Text] [Related]

  • 19. HGF/SF-met signaling in the control of branching morphogenesis and invasion.
    Zhang YW, Vande Woude GF.
    J Cell Biochem; 2003 Feb 01; 88(2):408-17. PubMed ID: 12520544
    [Abstract] [Full Text] [Related]

  • 20. Hepatocyte growth factor and Madin-Darby canine kidney cells: in vitro models of epithelial cell movement and morphogenesis.
    Balkovetz DF.
    Microsc Res Tech; 1998 Dec 01; 43(5):456-63. PubMed ID: 9858342
    [Abstract] [Full Text] [Related]

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