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Journal Abstract Search

345 related items for PubMed ID: 19013255

  • 1. Recruitment of HDAC4 by transcription factor YY1 represses HOXB13 to affect cell growth in AR-negative prostate cancers.
    Ren G, Zhang G, Dong Z, Liu Z, Li L, Feng Y, Su D, Zhang Y, Huang B, Lu J.
    Int J Biochem Cell Biol; 2009 May; 41(5):1094-101. PubMed ID: 19013255
    [Abstract] [Full Text] [Related]

  • 2. Recruitment of histone deacetylase 4 by transcription factors represses interleukin-5 transcription.
    Han S, Lu J, Zhang Y, Cheng C, Han L, Wang X, Li L, Liu C, Huang B.
    Biochem J; 2006 Dec 15; 400(3):439-48. PubMed ID: 16922677
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  • 3. HOXB13 induces growth suppression of prostate cancer cells as a repressor of hormone-activated androgen receptor signaling.
    Jung C, Kim RS, Zhang HJ, Lee SJ, Jeng MH.
    Cancer Res; 2004 Dec 15; 64(24):9185-92. PubMed ID: 15604291
    [Abstract] [Full Text] [Related]

  • 4. Binding of YY1 to the proximal region of the murine beta interferon promoter is essential to allow CBP recruitment and K8H4/K14H3 acetylation on the promoter region after virus infection.
    Mokrani H, Sharaf el Dein O, Mansuroglu Z, Bonnefoy E.
    Mol Cell Biol; 2006 Nov 15; 26(22):8551-61. PubMed ID: 16954376
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  • 5. Formation of AR-SMRT binding in prostate cancer cells treated with natural histone deacetylase inhibitor.
    Trtková K, Pašková L, Matiješčuková N, Kolář Z.
    Cancer Biomark; 2010 Nov 15; 7(2):79-90. PubMed ID: 21178266
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  • 7. Sodium butyrate regulates androgen receptor expression and cell cycle arrest in human prostate cancer cells.
    Kim J, Park H, Im JY, Choi WS, Kim HS.
    Anticancer Res; 2007 Nov 15; 27(5A):3285-92. PubMed ID: 17970072
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  • 8. HDAC4 represses p21(WAF1/Cip1) expression in human cancer cells through a Sp1-dependent, p53-independent mechanism.
    Mottet D, Pirotte S, Lamour V, Hagedorn M, Javerzat S, Bikfalvi A, Bellahcène A, Verdin E, Castronovo V.
    Oncogene; 2009 Jan 15; 28(2):243-56. PubMed ID: 18850004
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  • 10. The zinc finger repressor, ZBP-89, recruits histone deacetylase 1 to repress vimentin gene expression.
    Wu Y, Zhang X, Salmon M, Zehner ZE.
    Genes Cells; 2007 Aug 15; 12(8):905-18. PubMed ID: 17663720
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  • 12. De-repression of the p21 promoter in prostate cancer cells by an isothiocyanate via inhibition of HDACs and c-Myc.
    Wang LG, Liu XM, Fang Y, Dai W, Chiao FB, Puccio GM, Feng J, Liu D, Chiao JW.
    Int J Oncol; 2008 Aug 15; 33(2):375-80. PubMed ID: 18636159
    [Abstract] [Full Text] [Related]

  • 13. YY1 restrained cell senescence through repressing the transcription of p16.
    Wang X, Feng Y, Xu L, Chen Y, Zhang Y, Su D, Ren G, Lu J, Huang B.
    Biochim Biophys Acta; 2008 Oct 15; 1783(10):1876-83. PubMed ID: 18558095
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  • 15. FOXP1 is an androgen-responsive transcription factor that negatively regulates androgen receptor signaling in prostate cancer cells.
    Takayama K, Horie-Inoue K, Ikeda K, Urano T, Murakami K, Hayashizaki Y, Ouchi Y, Inoue S.
    Biochem Biophys Res Commun; 2008 Sep 19; 374(2):388-93. PubMed ID: 18640093
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  • 16. Inhibition of MAPK-signaling pathway promotes the interaction of the corepressor SMRT with the human androgen receptor and mediates repression of prostate cancer cell growth in the presence of antiandrogens.
    Eisold M, Asim M, Eskelinen H, Linke T, Baniahmad A.
    J Mol Endocrinol; 2009 May 19; 42(5):429-35. PubMed ID: 19223455
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  • 17. Statins increase p21 through inhibition of histone deacetylase activity and release of promoter-associated HDAC1/2.
    Lin YC, Lin JH, Chou CW, Chang YF, Yeh SH, Chen CC.
    Cancer Res; 2008 Apr 01; 68(7):2375-83. PubMed ID: 18381445
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  • 19. The Krüppel-like zinc-finger protein ZNF224 represses aldolase A gene transcription by interacting with the KAP-1 co-repressor protein.
    Medugno L, Florio F, De Cegli R, Grosso M, Lupo A, Costanzo P, Izzo P.
    Gene; 2005 Oct 10; 359():35-43. PubMed ID: 16150558
    [Abstract] [Full Text] [Related]

  • 20. Disruption of HDAC4/N-CoR complex by histone deacetylase inhibitors leads to inhibition of IL-2 gene expression.
    Matsuoka H, Fujimura T, Hayashi M, Matsuda K, Ishii Y, Aramori I, Mutoh S.
    Biochem Pharmacol; 2007 Aug 01; 74(3):465-76. PubMed ID: 17559812
    [Abstract] [Full Text] [Related]

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