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Journal Abstract Search

283 related items for PubMed ID: 8755515

  • 21. Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB.
    Wong CW, Privalsky ML.
    Mol Cell Biol; 1998 Sep; 18(9):5500-10. PubMed ID: 9710634
    [Abstract] [Full Text] [Related]

  • 22. The silencing mediator of retinoic acid and thyroid hormone receptor (SMRT) corepressor is required for full estrogen receptor alpha transcriptional activity.
    Peterson TJ, Karmakar S, Pace MC, Gao T, Smith CL.
    Mol Cell Biol; 2007 Sep; 27(17):5933-48. PubMed ID: 17591692
    [Abstract] [Full Text] [Related]

  • 23. The corepressors silencing mediator of retinoid and thyroid hormone receptor and nuclear receptor corepressor are involved in agonist- and antagonist-regulated transcription by androgen receptor.
    Yoon HG, Wong J.
    Mol Endocrinol; 2006 May; 20(5):1048-60. PubMed ID: 16373395
    [Abstract] [Full Text] [Related]

  • 24. Corepressor SMRT functions as a coactivator for thyroid hormone receptor T3Ralpha from a negative hormone response element.
    Berghagen H, Ragnhildstveit E, Krogsrud K, Thuestad G, Apriletti J, Saatcioglu F.
    J Biol Chem; 2002 Dec 20; 277(51):49517-22. PubMed ID: 12388540
    [Abstract] [Full Text] [Related]

  • 25. The nuclear corepressors recognize distinct nuclear receptor complexes.
    Cohen RN, Putney A, Wondisford FE, Hollenberg AN.
    Mol Endocrinol; 2000 Jun 20; 14(6):900-14. PubMed ID: 10847591
    [Abstract] [Full Text] [Related]

  • 26. Transcriptional repression by thyroid hormone receptors. A role for receptor homodimers in the recruitment of SMRT corepressor.
    Yoh SM, Privalsky ML.
    J Biol Chem; 2001 May 18; 276(20):16857-67. PubMed ID: 11278601
    [Abstract] [Full Text] [Related]

  • 27. The interaction of the vitamin D receptor with nuclear receptor corepressors and coactivators.
    Tagami T, Lutz WH, Kumar R, Jameson JL.
    Biochem Biophys Res Commun; 1998 Dec 18; 253(2):358-63. PubMed ID: 9878542
    [Abstract] [Full Text] [Related]

  • 28. Neuroanatomical distribution and colocalisation of nuclear receptor corepressor (N-CoR) and silencing mediator of retinoid and thyroid receptors (SMRT) in rat brain.
    van der Laan S, Lachize SB, Schouten TG, Vreugdenhil E, de Kloet ER, Meijer OC.
    Brain Res; 2005 Oct 19; 1059(2):113-21. PubMed ID: 16212947
    [Abstract] [Full Text] [Related]

  • 29. Two receptor interaction domains in the corepressor, N-CoR/RIP13, are required for an efficient interaction with Rev-erbA alpha and RVR: physical association is dependent on the E region of the orphan receptors.
    Downes M, Burke LJ, Bailey PJ, Muscat GE.
    Nucleic Acids Res; 1996 Nov 15; 24(22):4379-86. PubMed ID: 8948627
    [Abstract] [Full Text] [Related]

  • 30. Competitive cofactor recruitment by orphan receptor hepatocyte nuclear factor 4alpha1: modulation by the F domain.
    Ruse MD, Privalsky ML, Sladek FM.
    Mol Cell Biol; 2002 Mar 15; 22(6):1626-38. PubMed ID: 11865043
    [Abstract] [Full Text] [Related]

  • 31. Silencing mediator for retinoid and thyroid hormone receptors interacts with octamer transcription factor-1 and acts as a transcriptional repressor.
    Kakizawa T, Miyamoto T, Ichikawa K, Takeda T, Suzuki S, Mori J, Kumagai M, Yamashita K, Hashizume K.
    J Biol Chem; 2001 Mar 30; 276(13):9720-5. PubMed ID: 11134019
    [Abstract] [Full Text] [Related]

  • 32. Characterization of a strong repression domain in the hinge region of orphan nuclear receptor hB1F/hLRH-1.
    Xu PL, Shan SF, Kong YY, Xie YH, Wang Y.
    Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai); 2003 Oct 30; 35(10):909-16. PubMed ID: 14515208
    [Abstract] [Full Text] [Related]

  • 33. Interactions that determine the assembly of a retinoid X receptor/corepressor complex.
    Ghosh JC, Yang X, Zhang A, Lambert MH, Li H, Xu HE, Chen JD.
    Proc Natl Acad Sci U S A; 2002 Apr 30; 99(9):5842-7. PubMed ID: 11972046
    [Abstract] [Full Text] [Related]

  • 34. Involvement of SMRT corepressor in transcriptional repression by the vitamin D receptor.
    Kim JY, Son YL, Lee YC.
    Mol Endocrinol; 2009 Feb 30; 23(2):251-64. PubMed ID: 19098224
    [Abstract] [Full Text] [Related]

  • 35. Alternative splicing determines the interaction of SMRT isoforms with nuclear receptor-DNA complexes.
    Faist F, Short S, Kneale GG, Sharpe CR.
    Biosci Rep; 2009 Jun 30; 29(3):143-9. PubMed ID: 18752469
    [Abstract] [Full Text] [Related]

  • 36. The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70.
    Muscat GE, Burke LJ, Downes M.
    Nucleic Acids Res; 1998 Jun 15; 26(12):2899-907. PubMed ID: 9611234
    [Abstract] [Full Text] [Related]

  • 37. Nuclear receptor coregulators differentially modulate induction and glucocorticoid receptor-mediated repression of the corticotropin-releasing hormone gene.
    van der Laan S, Lachize SB, Vreugdenhil E, de Kloet ER, Meijer OC.
    Endocrinology; 2008 Feb 15; 149(2):725-32. PubMed ID: 18006628
    [Abstract] [Full Text] [Related]

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