These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


337 related items for PubMed ID: 12665580

  • 1. A multiplicity of coactivators is required by Gcn4p at individual promoters in vivo.
    Swanson MJ, Qiu H, Sumibcay L, Krueger A, Kim SJ, Natarajan K, Yoon S, Hinnebusch AG.
    Mol Cell Biol; 2003 Apr; 23(8):2800-20. PubMed ID: 12665580
    [Abstract] [Full Text] [Related]

  • 2. Recruitment of SWI/SNF by Gcn4p does not require Snf2p or Gcn5p but depends strongly on SWI/SNF integrity, SRB mediator, and SAGA.
    Yoon S, Qiu H, Swanson MJ, Hinnebusch AG.
    Mol Cell Biol; 2003 Dec; 23(23):8829-45. PubMed ID: 14612422
    [Abstract] [Full Text] [Related]

  • 3. 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; 25(13):5626-38. PubMed ID: 15964818
    [Abstract] [Full Text] [Related]

  • 4. An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p.
    Qiu H, Hu C, Yoon S, Natarajan K, Swanson MJ, Hinnebusch AG.
    Mol Cell Biol; 2004 May; 24(10):4104-17. PubMed ID: 15121833
    [Abstract] [Full Text] [Related]

  • 5. Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p.
    Qiu H, Hu C, Zhang F, Hwang GJ, Swanson MJ, Boonchird C, Hinnebusch AG.
    Mol Cell Biol; 2005 May; 25(9):3461-74. PubMed ID: 15831453
    [Abstract] [Full Text] [Related]

  • 6. A triad of subunits from the Gal11/tail domain of Srb mediator is an in vivo target of transcriptional activator Gcn4p.
    Zhang F, Sumibcay L, Hinnebusch AG, Swanson MJ.
    Mol Cell Biol; 2004 Aug; 24(15):6871-86. PubMed ID: 15254252
    [Abstract] [Full Text] [Related]

  • 7. The Gcn4p activation domain interacts specifically in vitro with RNA polymerase II holoenzyme, TFIID, and the Adap-Gcn5p coactivator complex.
    Drysdale CM, Jackson BM, McVeigh R, Klebanow ER, Bai Y, Kokubo T, Swanson M, Nakatani Y, Weil PA, Hinnebusch AG.
    Mol Cell Biol; 1998 Mar; 18(3):1711-24. PubMed ID: 9488488
    [Abstract] [Full Text] [Related]

  • 8. Activator Gcn4p and Cyc8p/Tup1p are interdependent for promoter occupancy at ARG1 in vivo.
    Kim SJ, Swanson MJ, Qiu H, Govind CK, Hinnebusch AG.
    Mol Cell Biol; 2005 Dec; 25(24):11171-83. PubMed ID: 16314536
    [Abstract] [Full Text] [Related]

  • 9. Transcriptional activation by Gcn4p involves independent interactions with the SWI/SNF complex and the SRB/mediator.
    Natarajan K, Jackson BM, Zhou H, Winston F, Hinnebusch AG.
    Mol Cell; 1999 Oct; 4(4):657-64. PubMed ID: 10549298
    [Abstract] [Full Text] [Related]

  • 10. A study of biochemical and functional interactions of Htl1p, a putative component of the Saccharomyces cerevisiae, Rsc chromatin-remodeling complex.
    Florio C, Moscariello M, Ederle S, Fasano R, Lanzuolo C, Pulitzer JF.
    Gene; 2007 Jun 15; 395(1-2):72-85. PubMed ID: 17400406
    [Abstract] [Full Text] [Related]

  • 11. Mediator, TATA-binding protein, and RNA polymerase II contribute to low histone occupancy at active gene promoters in yeast.
    Ansari SA, Paul E, Sommer S, Lieleg C, He Q, Daly AZ, Rode KA, Barber WT, Ellis LC, LaPorta E, Orzechowski AM, Taylor E, Reeb T, Wong J, Korber P, Morse RH.
    J Biol Chem; 2014 May 23; 289(21):14981-95. PubMed ID: 24727477
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. The activation specificities of wild-type and mutant Gcn4p in vivo can be different from the DNA binding specificities of the corresponding bZip peptides in vitro.
    Suckow M, Hollenberg CP.
    J Mol Biol; 1998 Mar 13; 276(5):887-902. PubMed ID: 9566194
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo.
    Bhaumik SR, Green MR.
    Mol Cell Biol; 2002 Nov 21; 22(21):7365-71. PubMed ID: 12370284
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Promoter occupancy is a major determinant of chromatin remodeling enzyme requirements.
    Dhasarathy A, Kladde MP.
    Mol Cell Biol; 2005 Apr 21; 25(7):2698-707. PubMed ID: 15767675
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 17.