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Journal Abstract Search

460 related items for PubMed ID: 9674426

  • 41. The novel SLIK histone acetyltransferase complex functions in the yeast retrograde response pathway.
    Pray-Grant MG, Schieltz D, McMahon SJ, Wood JM, Kennedy EL, Cook RG, Workman JL, Yates JR, Grant PA.
    Mol Cell Biol; 2002 Dec; 22(24):8774-86. PubMed ID: 12446794
    [Abstract] [Full Text] [Related]

  • 42. The SANT domain of Ada2 is required for normal acetylation of histones by the yeast SAGA complex.
    Sterner DE, Wang X, Bloom MH, Simon GM, Berger SL.
    J Biol Chem; 2002 Mar 08; 277(10):8178-86. PubMed ID: 11777910
    [Abstract] [Full Text] [Related]

  • 43. Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo.
    Govind CK, Yoon S, Qiu H, Govind S, Hinnebusch AG.
    Mol Cell Biol; 2005 Jul 08; 25(13):5626-38. PubMed ID: 15964818
    [Abstract] [Full Text] [Related]

  • 44. 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]

  • 45. Transcriptional activators direct histone acetyltransferase complexes to nucleosomes.
    Utley RT, Ikeda K, Grant PA, Côté J, Steger DJ, Eberharter A, John S, Workman JL.
    Nature; 1998 Jul 30; 394(6692):498-502. PubMed ID: 9697775
    [Abstract] [Full Text] [Related]

  • 46. Function and selectivity of bromodomains in anchoring chromatin-modifying complexes to promoter nucleosomes.
    Hassan AH, Prochasson P, Neely KE, Galasinski SC, Chandy M, Carrozza MJ, Workman JL.
    Cell; 2002 Nov 01; 111(3):369-79. PubMed ID: 12419247
    [Abstract] [Full Text] [Related]

  • 47. Stimulation of CREB binding protein nucleosomal histone acetyltransferase activity by a class of transcriptional activators.
    Chen CJ, Deng Z, Kim AY, Blobel GA, Lieberman PM.
    Mol Cell Biol; 2001 Jan 01; 21(2):476-87. PubMed ID: 11134336
    [Abstract] [Full Text] [Related]

  • 48. Robust mRNA transcription in chicken DT40 cells depleted of TAF(II)31 suggests both functional degeneracy and evolutionary divergence.
    Chen Z, Manley JL.
    Mol Cell Biol; 2000 Jul 01; 20(14):5064-76. PubMed ID: 10866663
    [Abstract] [Full Text] [Related]

  • 49. Acetylation of histones and transcription-related factors.
    Sterner DE, Berger SL.
    Microbiol Mol Biol Rev; 2000 Jun 01; 64(2):435-59. PubMed ID: 10839822
    [Abstract] [Full Text] [Related]

  • 50. Hyperacetylation of chromatin at the ADH2 promoter allows Adr1 to bind in repressed conditions.
    Verdone L, Wu J, van Riper K, Kacherovsky N, Vogelauer M, Young ET, Grunstein M, Di Mauro E, Caserta M.
    EMBO J; 2002 Mar 01; 21(5):1101-11. PubMed ID: 11867538
    [Abstract] [Full Text] [Related]

  • 51. Conformational flexibility and subunit arrangement of the modular yeast Spt-Ada-Gcn5 acetyltransferase complex.
    Setiaputra D, Ross JD, Lu S, Cheng DT, Dong MQ, Yip CK.
    J Biol Chem; 2015 Apr 17; 290(16):10057-70. PubMed ID: 25713136
    [Abstract] [Full Text] [Related]

  • 52. Role for Nhp6, Gcn5, and the Swi/Snf complex in stimulating formation of the TATA-binding protein-TFIIA-DNA complex.
    Biswas D, Imbalzano AN, Eriksson P, Yu Y, Stillman DJ.
    Mol Cell Biol; 2004 Sep 17; 24(18):8312-21. PubMed ID: 15340090
    [Abstract] [Full Text] [Related]

  • 53. The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.
    Sudarsanam P, Cao Y, Wu L, Laurent BC, Winston F.
    EMBO J; 1999 Jun 01; 18(11):3101-6. PubMed ID: 10357821
    [Abstract] [Full Text] [Related]

  • 54. Differential requirement of SAGA subunits for Mot1p and Taf1p recruitment in gene activation.
    van Oevelen CJ, van Teeffelen HA, Timmers HT.
    Mol Cell Biol; 2005 Jun 01; 25(12):4863-72. PubMed ID: 15923605
    [Abstract] [Full Text] [Related]

  • 55. A transient histone hyperacetylation signal marks nucleosomes for remodeling at the PHO8 promoter in vivo.
    Reinke H, Gregory PD, Hörz W.
    Mol Cell; 2001 Mar 01; 7(3):529-38. PubMed ID: 11463378
    [Abstract] [Full Text] [Related]

  • 56. Histone acetyltransferase activity is conserved between yeast and human GCN5 and is required for complementation of growth and transcriptional activation.
    Wang L, Mizzen C, Ying C, Candau R, Barlev N, Brownell J, Allis CD, Berger SL.
    Mol Cell Biol; 1997 Jan 01; 17(1):519-27. PubMed ID: 8972232
    [Abstract] [Full Text] [Related]

  • 57. A human SPT3-TAFII31-GCN5-L acetylase complex distinct from transcription factor IID.
    Martinez E, Kundu TK, Fu J, Roeder RG.
    J Biol Chem; 1998 Sep 11; 273(37):23781-5. PubMed ID: 9726987
    [Abstract] [Full Text] [Related]

  • 58. Molecular architecture of the S. cerevisiae SAGA complex.
    Wu PY, Ruhlmann C, Winston F, Schultz P.
    Mol Cell; 2004 Jul 23; 15(2):199-208. PubMed ID: 15260971
    [Abstract] [Full Text] [Related]

  • 59. Overlapping roles for the histone acetyltransferase activities of SAGA and elongator in vivo.
    Wittschieben BO, Fellows J, Du W, Stillman DJ, Svejstrup JQ.
    EMBO J; 2000 Jun 15; 19(12):3060-8. PubMed ID: 10856249
    [Abstract] [Full Text] [Related]

  • 60. TAFII55 binding to TAFII250 inhibits its acetyltransferase activity.
    Gegonne A, Weissman JD, Singer DS.
    Proc Natl Acad Sci U S A; 2001 Oct 23; 98(22):12432-7. PubMed ID: 11592977
    [Abstract] [Full Text] [Related]

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