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Journal Abstract Search

545 related items for PubMed ID: 10357821

  • 21. Histone acetyltransferase complexes stabilize swi/snf binding to promoter nucleosomes.
    Hassan AH, Neely KE, Workman JL.
    Cell; 2001 Mar 23; 104(6):817-27. PubMed ID: 11290320
    [Abstract] [Full Text] [Related]

  • 22. Histone H2A.Z regulats transcription and is partially redundant with nucleosome remodeling complexes.
    Santisteban MS, Kalashnikova T, Smith MM.
    Cell; 2000 Oct 27; 103(3):411-22. PubMed ID: 11081628
    [Abstract] [Full Text] [Related]

  • 23. Role for ADA/GCN5 products in antagonizing chromatin-mediated transcriptional repression.
    Pollard KJ, Peterson CL.
    Mol Cell Biol; 1997 Nov 27; 17(11):6212-22. PubMed ID: 9343382
    [Abstract] [Full Text] [Related]

  • 24. Swi/SNF-GCN5-dependent chromatin remodelling determines induced expression of GDH3, one of the paralogous genes responsible for ammonium assimilation and glutamate biosynthesis in Saccharomyces cerevisiae.
    Avendaño A, Riego L, DeLuna A, Aranda C, Romero G, Ishida C, Vázquez-Acevedo M, Rodarte B, Recillas-Targa F, Valenzuela L, Zonszein S, González A.
    Mol Microbiol; 2005 Jul 27; 57(1):291-305. PubMed ID: 15948967
    [Abstract] [Full Text] [Related]

  • 25. Global role for chromatin remodeling enzymes in mitotic gene expression.
    Krebs JE, Fry CJ, Samuels ML, Peterson CL.
    Cell; 2000 Sep 01; 102(5):587-98. PubMed ID: 11007477
    [Abstract] [Full Text] [Related]

  • 26. Nucleosome disruption and enhancement of activator binding by a human SW1/SNF complex.
    Kwon H, Imbalzano AN, Khavari PA, Kingston RE, Green MR.
    Nature; 1994 Aug 11; 370(6489):477-81. PubMed ID: 8047169
    [Abstract] [Full Text] [Related]

  • 27. Antagonistic remodelling by Swi-Snf and Tup1-Ssn6 of an extensive chromatin region forms the background for FLO1 gene regulation.
    Fleming AB, Pennings S.
    EMBO J; 2001 Sep 17; 20(18):5219-31. PubMed ID: 11566885
    [Abstract] [Full Text] [Related]

  • 28. SWI/SNF binding to the HO promoter requires histone acetylation and stimulates TATA-binding protein recruitment.
    Mitra D, Parnell EJ, Landon JW, Yu Y, Stillman DJ.
    Mol Cell Biol; 2006 Jun 17; 26(11):4095-110. PubMed ID: 16705163
    [Abstract] [Full Text] [Related]

  • 29. Histone acetyltransferase activity and interaction with ADA2 are critical for GCN5 function in vivo.
    Candau R, Zhou JX, Allis CD, Berger SL.
    EMBO J; 1997 Feb 03; 16(3):555-65. PubMed ID: 9034338
    [Abstract] [Full Text] [Related]

  • 30. Activation of Saccharomyces cerevisiae HIS3 results in Gcn4p-dependent, SWI/SNF-dependent mobilization of nucleosomes over the entire gene.
    Kim Y, McLaughlin N, Lindstrom K, Tsukiyama T, Clark DJ.
    Mol Cell Biol; 2006 Nov 03; 26(22):8607-22. PubMed ID: 16982689
    [Abstract] [Full Text] [Related]

  • 31. GCN5 dependence of chromatin remodeling and transcriptional activation by the GAL4 and VP16 activation domains in budding yeast.
    Stafford GA, Morse RH.
    Mol Cell Biol; 2001 Jul 03; 21(14):4568-78. PubMed ID: 11416135
    [Abstract] [Full Text] [Related]

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  • 34. Interplay of yeast global transcriptional regulators Ssn6p-Tup1p and Swi-Snf and their effect on chromatin structure.
    Gavin IM, Simpson RT.
    EMBO J; 1997 Oct 15; 16(20):6263-71. PubMed ID: 9321405
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  • 35. Adenovirus E1A requires the yeast SAGA histone acetyltransferase complex and associates with SAGA components Gcn5 and Tra1.
    Kulesza CA, Van Buskirk HA, Cole MD, Reese JC, Smith MM, Engel DA.
    Oncogene; 2002 Feb 21; 21(9):1411-22. PubMed ID: 11857084
    [Abstract] [Full Text] [Related]

  • 36. Functional interaction between GCN5 and polyamines: a new role for core histone acetylation.
    Pollard KJ, Samuels ML, Crowley KA, Hansen JC, Peterson CL.
    EMBO J; 1999 Oct 15; 18(20):5622-33. PubMed ID: 10523306
    [Abstract] [Full Text] [Related]

  • 37. Evidence that Swi/Snf directly represses transcription in S. cerevisiae.
    Martens JA, Winston F.
    Genes Dev; 2002 Sep 01; 16(17):2231-6. PubMed ID: 12208846
    [Abstract] [Full Text] [Related]

  • 38. The core histone N-terminal domains are required for multiple rounds of catalytic chromatin remodeling by the SWI/SNF and RSC complexes.
    Logie C, Tse C, Hansen JC, Peterson CL.
    Biochemistry; 1999 Feb 23; 38(8):2514-22. PubMed ID: 10029546
    [Abstract] [Full Text] [Related]

  • 39. SWI/SNF-dependent chromatin remodeling of RNR3 requires TAF(II)s and the general transcription machinery.
    Sharma VM, Li B, Reese JC.
    Genes Dev; 2003 Feb 15; 17(4):502-15. PubMed ID: 12600943
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