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Journal Abstract Search

273 related items for PubMed ID: 9106656

  • 1. Stoichiometric and steric principles governing repression by nuclear hormone receptors.
    Zamir I, Zhang J, Lazar MA.
    Genes Dev; 1997 Apr 01; 11(7):835-46. PubMed ID: 9106656
    [Abstract] [Full Text] [Related]

  • 2. Characterization of receptor interaction and transcriptional repression by the corepressor SMRT.
    Li H, Leo C, Schroen DJ, Chen JD.
    Mol Endocrinol; 1997 Dec 01; 11(13):2025-37. PubMed ID: 9415406
    [Abstract] [Full Text] [Related]

  • 3. N-CoR-HDAC corepressor complexes: roles in transcriptional regulation by nuclear hormone receptors.
    Jones PL, Shi YB.
    Curr Top Microbiol Immunol; 2003 Dec 01; 274():237-68. PubMed ID: 12596910
    [Abstract] [Full Text] [Related]

  • 4. The specificity of interactions between nuclear hormone receptors and corepressors is mediated by distinct amino acid sequences within the interacting domains.
    Cohen RN, Brzostek S, Kim B, Chorev M, Wondisford FE, Hollenberg AN.
    Mol Endocrinol; 2001 Jul 01; 15(7):1049-61. PubMed ID: 11435607
    [Abstract] [Full Text] [Related]

  • 5. Gene silencing by chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is mediated by transcriptional corepressors, nuclear receptor-corepressor (N-CoR) and silencing mediator for retinoic acid receptor and thyroid hormone receptor (SMRT).
    Shibata H, Nawaz Z, Tsai SY, O'Malley BW, Tsai MJ.
    Mol Endocrinol; 1997 Jun 01; 11(6):714-24. PubMed ID: 9171235
    [Abstract] [Full Text] [Related]

  • 6. Signaling by tyrosine kinases negatively regulates the interaction between transcription factors and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) corepressor.
    Hong SH, Wong CW, Privalsky ML.
    Mol Endocrinol; 1998 Aug 01; 12(8):1161-71. PubMed ID: 9717842
    [Abstract] [Full Text] [Related]

  • 7. The nuclear corepressors recognize distinct nuclear receptor complexes.
    Cohen RN, Putney A, Wondisford FE, Hollenberg AN.
    Mol Endocrinol; 2000 Jun 01; 14(6):900-14. PubMed ID: 10847591
    [Abstract] [Full Text] [Related]

  • 8. Differential effects of nuclear receptor corepressor (N-CoR) expression levels on retinoic acid receptor-mediated repression support the existence of dynamically regulated corepressor complexes.
    Söderström M, Vo A, Heinzel T, Lavinsky RM, Yang WM, Seto E, Peterson DA, Rosenfeld MG, Glass CK.
    Mol Endocrinol; 1997 Jun 01; 11(6):682-92. PubMed ID: 9171232
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Very strong correlation between dominant negative activities of mutant thyroid hormone receptors and their binding avidity for corepressor SMRT.
    Matsushita A, Misawa H, Andoh S, Natsume H, Nishiyama K, Sasaki S, Nakamura H.
    J Endocrinol; 2000 Dec 18; 167(3):493-503. PubMed ID: 11115777
    [Abstract] [Full Text] [Related]

  • 11. Transcriptional silencing is defined by isoform- and heterodimer-specific interactions between nuclear hormone receptors and corepressors.
    Wong CW, Privalsky ML.
    Mol Cell Biol; 1998 Oct 18; 18(10):5724-33. PubMed ID: 9742089
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Response of SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) and N-CoR (nuclear receptor corepressor) corepressors to mitogen-activated protein kinase kinase kinase cascades is determined by alternative mRNA splicing.
    Jonas BA, Varlakhanova N, Hayakawa F, Goodson M, Privalsky ML.
    Mol Endocrinol; 2007 Aug 15; 21(8):1924-39. PubMed ID: 17519355
    [Abstract] [Full Text] [Related]

  • 14. Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3.
    Li J, Wang J, Wang J, Nawaz Z, Liu JM, Qin J, Wong J.
    EMBO J; 2000 Aug 15; 19(16):4342-50. PubMed ID: 10944117
    [Abstract] [Full Text] [Related]

  • 15. SMRT and N-CoR corepressors are regulated by distinct kinase signaling pathways.
    Jonas BA, Privalsky ML.
    J Biol Chem; 2004 Dec 24; 279(52):54676-86. PubMed ID: 15491994
    [Abstract] [Full Text] [Related]

  • 16. Recruitment of N-CoR/SMRT-TBLR1 corepressor complex by unliganded thyroid hormone receptor for gene repression during frog development.
    Tomita A, Buchholz DR, Shi YB.
    Mol Cell Biol; 2004 Apr 24; 24(8):3337-46. PubMed ID: 15060155
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Oligomerization of ETO is obligatory for corepressor interaction.
    Zhang J, Hug BA, Huang EY, Chen CW, Gelmetti V, Maccarana M, Minucci S, Pelicci PG, Lazar MA.
    Mol Cell Biol; 2001 Jan 15; 21(1):156-63. PubMed ID: 11113190
    [Abstract] [Full Text] [Related]

  • 19. SMRT isoforms mediate repression and anti-repression of nuclear receptor heterodimers.
    Chen JD, Umesono K, Evans RM.
    Proc Natl Acad Sci U S A; 1996 Jul 23; 93(15):7567-71. PubMed ID: 8755515
    [Abstract] [Full Text] [Related]

  • 20. Characterization of the repressor function of the nuclear orphan receptor retinoid receptor-related testis-associated receptor/germ cell nuclear factor.
    Yan Z, Jetten AM.
    J Biol Chem; 2000 Nov 10; 275(45):35077-85. PubMed ID: 10940306
    [Abstract] [Full Text] [Related]

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