BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

575 related articles for article (PubMed ID: 9139820)

  • 1. A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression.
    Heinzel T; Lavinsky RM; Mullen TM; Söderstrom M; Laherty CD; Torchia J; Yang WM; Brard G; Ngo SD; Davie JR; Seto E; Eisenman RN; Rose DW; Glass CK; Rosenfeld MG
    Nature; 1997 May; 387(6628):43-8. PubMed ID: 9139820
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression.
    Alland L; Muhle R; Hou H; Potes J; Chin L; Schreiber-Agus N; DePinho RA
    Nature; 1997 May; 387(6628):49-55. PubMed ID: 9139821
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transcriptional control. Sinful repression.
    Wolffe AP
    Nature; 1997 May; 387(6628):16-7. PubMed ID: 9139815
    [No Abstract]   [Full Text] [Related]  

  • 4. The functional relationship between co-repressor N-CoR and SMRT in mediating transcriptional repression by thyroid hormone receptor alpha.
    Choi KC; Oh SY; Kang HB; Lee YH; Haam S; Kim HI; Kim K; Ahn YH; Kim KS; Yoon HG
    Biochem J; 2008 Apr; 411(1):19-26. PubMed ID: 18052923
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Repression by the Mad(Mxi1)-Sin3 complex.
    Schreiber-Agus N; DePinho RA
    Bioessays; 1998 Oct; 20(10):808-18. PubMed ID: 9819568
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Modulation of thyroid hormone receptor silencing function by co-repressors and a synergizing transcription factor.
    Lutz M; Baniahmad A; Renkawitz R
    Biochem Soc Trans; 2000; 28(4):386-9. PubMed ID: 10961925
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Targeting of N-CoR and histone deacetylase 3 by the oncoprotein v-erbA yields a chromatin infrastructure-dependent transcriptional repression pathway.
    Urnov FD; Yee J; Sachs L; Collingwood TN; Bauer A; Beug H; Shi YB; Wolffe AP
    EMBO J; 2000 Aug; 19(15):4074-90. PubMed ID: 10921888
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor.
    Hörlein AJ; Näär AM; Heinzel T; Torchia J; Gloss B; Kurokawa R; Ryan A; Kamei Y; Söderström M; Glass CK
    Nature; 1995 Oct; 377(6548):397-404. PubMed ID: 7566114
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biological activity of mammalian transcriptional repressors.
    Thiel G; Lietz M; Bach K; Guethlein L; Cibelli G
    Biol Chem; 2001 Jun; 382(6):891-902. PubMed ID: 11501753
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Coactivator and corepressor complexes in nuclear receptor function.
    Xu L; Glass CK; Rosenfeld MG
    Curr Opin Genet Dev; 1999 Apr; 9(2):140-7. PubMed ID: 10322133
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SAP30, a component of the mSin3 corepressor complex involved in N-CoR-mediated repression by specific transcription factors.
    Laherty CD; Billin AN; Lavinsky RM; Yochum GS; Bush AC; Sun JM; Mullen TM; Davie JR; Rose DW; Glass CK; Rosenfeld MG; Ayer DE; Eisenman RN
    Mol Cell; 1998 Jul; 2(1):33-42. PubMed ID: 9702189
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Co-repressor SMRT and class II histone deacetylases promote Bach2 nuclear retention and formation of nuclear foci that are responsible for local transcriptional repression.
    Hoshino H; Nishino TG; Tashiro S; Miyazaki M; Ohmiya Y; Igarashi K; Horinouchi S; Yoshida M
    J Biochem; 2007 May; 141(5):719-27. PubMed ID: 17383980
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Histone deacetylase associated with mSin3A mediates repression by the acute promyelocytic leukemia-associated PLZF protein.
    David G; Alland L; Hong SH; Wong CW; DePinho RA; Dejean A
    Oncogene; 1998 May; 16(19):2549-56. PubMed ID: 9627120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. TEL contacts multiple co-repressors and specifically associates with histone deacetylase-3.
    Wang L; Hiebert SW
    Oncogene; 2001 Jun; 20(28):3716-25. PubMed ID: 11439334
    [TBL] [Abstract][Full Text] [Related]  

  • 15. FEV acts as a transcriptional repressor through its DNA-binding ETS domain and alanine-rich domain.
    Maurer P; T'Sas F; Coutte L; Callens N; Brenner C; Van Lint C; de Launoit Y; Baert JL
    Oncogene; 2003 May; 22(21):3319-29. PubMed ID: 12761502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prohibitin co-localizes with Rb in the nucleus and recruits N-CoR and HDAC1 for transcriptional repression.
    Wang S; Fusaro G; Padmanabhan J; Chellappan SP
    Oncogene; 2002 Dec; 21(55):8388-96. PubMed ID: 12466959
    [TBL] [Abstract][Full Text] [Related]  

  • 17. JMJD2A is a novel N-CoR-interacting protein and is involved in repression of the human transcription factor achaete scute-like homologue 2 (ASCL2/Hash2).
    Zhang D; Yoon HG; Wong J
    Mol Cell Biol; 2005 Aug; 25(15):6404-14. PubMed ID: 16024779
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 11(6):682-92. PubMed ID: 9171232
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor.
    Nomura T; Khan MM; Kaul SC; Dong HD; Wadhwa R; Colmenares C; Kohno I; Ishii S
    Genes Dev; 1999 Feb; 13(4):412-23. PubMed ID: 10049357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mad proteins contain a dominant transcription repression domain.
    Ayer DE; Laherty CD; Lawrence QA; Armstrong AP; Eisenman RN
    Mol Cell Biol; 1996 Oct; 16(10):5772-81. PubMed ID: 8816491
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 29.