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197 related items for PubMed ID: 15065872

  • 1. Distinct activation mechanisms of protein kinase B by growth-factor stimulation and heat-shock treatment.
    Matsuzaki H, Yamamoto T, Kikkawa U.
    Biochemistry; 2004 Apr 13; 43(14):4284-93. PubMed ID: 15065872
    [Abstract] [Full Text] [Related]

  • 2. Akt activation by growth factors is a multiple-step process: the role of the PH domain.
    Bellacosa A, Chan TO, Ahmed NN, Datta K, Malstrom S, Stokoe D, McCormick F, Feng J, Tsichlis P.
    Oncogene; 1998 Jul 23; 17(3):313-25. PubMed ID: 9690513
    [Abstract] [Full Text] [Related]

  • 3. Role of phosphatidylinositol 3,4,5-trisphosphate in regulating the activity and localization of 3-phosphoinositide-dependent protein kinase-1.
    Currie RA, Walker KS, Gray A, Deak M, Casamayor A, Downes CP, Cohen P, Alessi DR, Lucocq J.
    Biochem J; 1999 Feb 01; 337 ( Pt 3)(Pt 3):575-83. PubMed ID: 9895304
    [Abstract] [Full Text] [Related]

  • 4. The pleckstrin homology domains of protein kinase B and GRP1 (general receptor for phosphoinositides-1) are sensitive and selective probes for the cellular detection of phosphatidylinositol 3,4-bisphosphate and/or phosphatidylinositol 3,4,5-trisphosphate in vivo.
    Gray A, Van Der Kaay J, Downes CP.
    Biochem J; 1999 Dec 15; 344 Pt 3(Pt 3):929-36. PubMed ID: 10585883
    [Abstract] [Full Text] [Related]

  • 5. Growth factor-induced signaling of the pancreatic epithelium.
    Kayali AG, Stotland A, Gunst KV, Kritzik M, Liu G, Dabernat S, Zhang YQ, Wu W, Sarvetnick N.
    J Endocrinol; 2005 Apr 15; 185(1):45-56. PubMed ID: 15817826
    [Abstract] [Full Text] [Related]

  • 6. Binding of phosphatidylinositol 3,4,5-trisphosphate to the pleckstrin homology domain of protein kinase B induces a conformational change.
    Milburn CC, Deak M, Kelly SM, Price NC, Alessi DR, Van Aalten DM.
    Biochem J; 2003 Nov 01; 375(Pt 3):531-8. PubMed ID: 12964941
    [Abstract] [Full Text] [Related]

  • 7. The protein-tyrosine phosphatase DEP-1 modulates growth factor-stimulated cell migration and cell-matrix adhesion.
    Jandt E, Denner K, Kovalenko M, Ostman A, Böhmer FD.
    Oncogene; 2003 Jul 03; 22(27):4175-85. PubMed ID: 12833140
    [Abstract] [Full Text] [Related]

  • 8. Receptor association and tyrosine phosphorylation of S6 kinases.
    Rebholz H, Panasyuk G, Fenton T, Nemazanyy I, Valovka T, Flajolet M, Ronnstrand L, Stephens L, West A, Gout IT.
    FEBS J; 2006 May 03; 273(9):2023-36. PubMed ID: 16640565
    [Abstract] [Full Text] [Related]

  • 9. Inactivation and dephosphorylation of protein kinase Balpha (PKBalpha) promoted by hyperosmotic stress.
    Meier R, Thelen M, Hemmings BA.
    EMBO J; 1998 Dec 15; 17(24):7294-303. PubMed ID: 9857186
    [Abstract] [Full Text] [Related]

  • 10. Different cellular localization, translocation, and insulin-induced phosphorylation of PKBalpha in HepG2 cells and hepatocytes.
    Syed NA, Horner KN, Misra V, Khandelwal RL.
    J Cell Biochem; 2002 Dec 15; 86(1):118-27. PubMed ID: 12112022
    [Abstract] [Full Text] [Related]

  • 11. Phosphatidylinositol 3-kinase (PI-3K)/Akt but not PI-3K/p70 S6 kinase signaling mediates IGF-1-promoted lens epithelial cell survival.
    Chandrasekher G, Sailaja D.
    Invest Ophthalmol Vis Sci; 2004 Oct 15; 45(10):3577-88. PubMed ID: 15452065
    [Abstract] [Full Text] [Related]

  • 12. Regulation of protein kinase B.
    Meier R, Hemmings BA.
    J Recept Signal Transduct Res; 1999 Oct 15; 19(1-4):121-8. PubMed ID: 10071752
    [Abstract] [Full Text] [Related]

  • 13. Mitogen-activated protein kinases Erk1/2 and p38 are required for maximal regulation of TIMP-1 by oncostatin M in murine fibroblasts.
    Tong L, Smyth D, Kerr C, Catterall J, Richards CD.
    Cell Signal; 2004 Oct 15; 16(10):1123-32. PubMed ID: 15240007
    [Abstract] [Full Text] [Related]

  • 14. Two distinct regulatory mechanisms of neurotransmitter release by phosphatidylinositol 3-kinase.
    Itakura M, Yamamori S, Kuwahara R, Sekiguchi M, Takahashi M.
    J Neurochem; 2005 Jul 15; 94(2):502-9. PubMed ID: 15998300
    [Abstract] [Full Text] [Related]

  • 15. Cell-type specific phosphorylation of threonines T654 and T669 by PKD defines the signal capacity of the EGF receptor.
    Bagowski CP, Stein-Gerlach M, Choidas A, Ullrich A.
    EMBO J; 1999 Oct 15; 18(20):5567-76. PubMed ID: 10523301
    [Abstract] [Full Text] [Related]

  • 16. Requirement of the serine-threonine kinase Akt for heat treatment-induced activation of p70 S6 kinase.
    Kuroda S, Ogawa W, Kitamura T, Konishi H, Kikkawa U, Kasuga M.
    Biochem Biophys Res Commun; 1998 Aug 28; 249(3):781-5. PubMed ID: 9731213
    [Abstract] [Full Text] [Related]

  • 17. Carboxyl-terminal modulator protein (CTMP), a negative regulator of PKB/Akt and v-Akt at the plasma membrane.
    Maira SM, Galetic I, Brazil DP, Kaech S, Ingley E, Thelen M, Hemmings BA.
    Science; 2001 Oct 12; 294(5541):374-80. PubMed ID: 11598301
    [Abstract] [Full Text] [Related]

  • 18. Activation of serum- and glucocorticoid-regulated protein kinase by agonists that activate phosphatidylinositide 3-kinase is mediated by 3-phosphoinositide-dependent protein kinase-1 (PDK1) and PDK2.
    Kobayashi T, Cohen P.
    Biochem J; 1999 Apr 15; 339 ( Pt 2)(Pt 2):319-28. PubMed ID: 10191262
    [Abstract] [Full Text] [Related]

  • 19. Effect of overexpression and nuclear translocation of constitutively active PKB-alpha on cellular survival and proliferation in HepG2 cells.
    Gupta D, Syed NA, Roesler WJ, Khandelwal RL.
    J Cell Biochem; 2004 Oct 15; 93(3):513-25. PubMed ID: 15372623
    [Abstract] [Full Text] [Related]

  • 20. Mutations of critical amino acids affect the biological and biochemical properties of oncogenic A-Raf and Raf-1.
    Bosch E, Cherwinski H, Peterson D, McMahon M.
    Oncogene; 1997 Aug 28; 15(9):1021-33. PubMed ID: 9285556
    [Abstract] [Full Text] [Related]

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