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Journal Abstract Search


259 related items for PubMed ID: 12489981

  • 1. Heat-shock protein 90 and Cdc37 interact with LKB1 and regulate its stability.
    Boudeau J, Deak M, Lawlor MA, Morrice NA, Alessi DR.
    Biochem J; 2003 Mar 15; 370(Pt 3):849-57. PubMed ID: 12489981
    [Abstract] [Full Text] [Related]

  • 2. Stability of the Peutz-Jeghers syndrome kinase LKB1 requires its binding to the molecular chaperones Hsp90/Cdc37.
    Nony P, Gaude H, Rossel M, Fournier L, Rouault JP, Billaud M.
    Oncogene; 2003 Dec 11; 22(57):9165-75. PubMed ID: 14668798
    [Abstract] [Full Text] [Related]

  • 3. Molecular chaperone complexes with antagonizing activities regulate stability and activity of the tumor suppressor LKB1.
    Gaude H, Aznar N, Delay A, Bres A, Buchet-Poyau K, Caillat C, Vigouroux A, Rogon C, Woods A, Vanacker JM, Höhfeld J, Perret C, Meyer P, Billaud M, Forcet C.
    Oncogene; 2012 Mar 22; 31(12):1582-91. PubMed ID: 21860411
    [Abstract] [Full Text] [Related]

  • 4. Specific association of a set of molecular chaperones including HSP90 and Cdc37 with MOK, a member of the mitogen-activated protein kinase superfamily.
    Miyata Y, Ikawa Y, Shibuya M, Nishida E.
    J Biol Chem; 2001 Jun 15; 276(24):21841-8. PubMed ID: 11278794
    [Abstract] [Full Text] [Related]

  • 5. Akt forms an intracellular complex with heat shock protein 90 (Hsp90) and Cdc37 and is destabilized by inhibitors of Hsp90 function.
    Basso AD, Solit DB, Chiosis G, Giri B, Tsichlis P, Rosen N.
    J Biol Chem; 2002 Oct 18; 277(42):39858-66. PubMed ID: 12176997
    [Abstract] [Full Text] [Related]

  • 6. p50(cdc37) acting in concert with Hsp90 is required for Raf-1 function.
    Grammatikakis N, Lin JH, Grammatikakis A, Tsichlis PN, Cochran BH.
    Mol Cell Biol; 1999 Mar 18; 19(3):1661-72. PubMed ID: 10022854
    [Abstract] [Full Text] [Related]

  • 7. The heat shock protein 90 antagonist geldanamycin alters chaperone association with p210bcr-abl and v-src proteins before their degradation by the proteasome.
    An WG, Schulte TW, Neckers LM.
    Cell Growth Differ; 2000 Jul 18; 11(7):355-60. PubMed ID: 10939589
    [Abstract] [Full Text] [Related]

  • 8. Hsp90/p50cdc37 is required for mixed-lineage kinase (MLK) 3 signaling.
    Zhang H, Wu W, Du Y, Santos SJ, Conrad SE, Watson JT, Grammatikakis N, Gallo KA.
    J Biol Chem; 2004 May 07; 279(19):19457-63. PubMed ID: 15001580
    [Abstract] [Full Text] [Related]

  • 9. Hsp90 regulates p50(cdc37) function during the biogenesis of the activeconformation of the heme-regulated eIF2 alpha kinase.
    Shao J, Grammatikakis N, Scroggins BT, Uma S, Huang W, Chen JJ, Hartson SD, Matts RL.
    J Biol Chem; 2001 Jan 05; 276(1):206-14. PubMed ID: 11036079
    [Abstract] [Full Text] [Related]

  • 10. TNF-induced recruitment and activation of the IKK complex require Cdc37 and Hsp90.
    Chen G, Cao P, Goeddel DV.
    Mol Cell; 2002 Feb 05; 9(2):401-10. PubMed ID: 11864612
    [Abstract] [Full Text] [Related]

  • 11. Protein quality control of DYRK family protein kinases by the Hsp90-Cdc37 molecular chaperone.
    Miyata Y, Nishida E.
    Biochim Biophys Acta Mol Cell Res; 2021 Sep 05; 1868(10):119081. PubMed ID: 34147560
    [Abstract] [Full Text] [Related]

  • 12. Coordinated regulation of serum- and glucocorticoid-inducible kinase 3 by a C-terminal hydrophobic motif and Hsp90-Cdc37 chaperone complex.
    Wang Y, Xu W, Zhou D, Neckers L, Chen S.
    J Biol Chem; 2014 Feb 21; 289(8):4815-26. PubMed ID: 24379398
    [Abstract] [Full Text] [Related]

  • 13. Heat shock protein 90 modulates the unfolded protein response by stabilizing IRE1alpha.
    Marcu MG, Doyle M, Bertolotti A, Ron D, Hendershot L, Neckers L.
    Mol Cell Biol; 2002 Dec 21; 22(24):8506-13. PubMed ID: 12446770
    [Abstract] [Full Text] [Related]

  • 14. Specific regulation of noncanonical p38alpha activation by Hsp90-Cdc37 chaperone complex in cardiomyocyte.
    Ota A, Zhang J, Ping P, Han J, Wang Y.
    Circ Res; 2010 Apr 30; 106(8):1404-12. PubMed ID: 20299663
    [Abstract] [Full Text] [Related]

  • 15. L347P PINK1 mutant that fails to bind to Hsp90/Cdc37 chaperones is rapidly degraded in a proteasome-dependent manner.
    Moriwaki Y, Kim YJ, Ido Y, Misawa H, Kawashima K, Endo S, Takahashi R.
    Neurosci Res; 2008 May 30; 61(1):43-8. PubMed ID: 18359116
    [Abstract] [Full Text] [Related]

  • 16. Cdk2: a genuine protein kinase client of Hsp90 and Cdc37.
    Prince T, Sun L, Matts RL.
    Biochemistry; 2005 Nov 22; 44(46):15287-95. PubMed ID: 16285732
    [Abstract] [Full Text] [Related]

  • 17. Differential effects of Hsp90 inhibition on protein kinases regulating signal transduction pathways required for myoblast differentiation.
    Yun BG, Matts RL.
    Exp Cell Res; 2005 Jul 01; 307(1):212-23. PubMed ID: 15922741
    [Abstract] [Full Text] [Related]

  • 18. Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome.
    Loo MA, Jensen TJ, Cui L, Hou Y, Chang XB, Riordan JR.
    EMBO J; 1998 Dec 01; 17(23):6879-87. PubMed ID: 9843494
    [Abstract] [Full Text] [Related]

  • 19. Cdc37 goes beyond Hsp90 and kinases.
    MacLean M, Picard D.
    Cell Stress Chaperones; 2003 Dec 01; 8(2):114-9. PubMed ID: 14627196
    [Abstract] [Full Text] [Related]

  • 20. Identification of a DYRK1A Inhibitor that Induces Degradation of the Target Kinase using Co-chaperone CDC37 fused with Luciferase nanoKAZ.
    Sonamoto R, Kii I, Koike Y, Sumida Y, Kato-Sumida T, Okuno Y, Hosoya T, Hagiwara M.
    Sci Rep; 2015 Aug 03; 5():12728. PubMed ID: 26234946
    [Abstract] [Full Text] [Related]


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