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Journal Abstract Search

267 related items for PubMed ID: 9488488

  • 1. 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]

  • 2. yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex.
    Natarajan K, Jackson BM, Rhee E, Hinnebusch AG.
    Mol Cell; 1998 Nov; 2(5):683-92. PubMed ID: 9844640
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. 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]

  • 7. 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]

  • 8. ADR1-mediated transcriptional activation requires the presence of an intact TFIID complex.
    Komarnitsky PB, Klebanow ER, Weil PA, Denis CL.
    Mol Cell Biol; 1998 Oct; 18(10):5861-7. PubMed ID: 9742103
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. An activator binding module of yeast RNA polymerase II holoenzyme.
    Lee YC, Park JM, Min S, Han SJ, Kim YJ.
    Mol Cell Biol; 1999 Apr; 19(4):2967-76. PubMed ID: 10082564
    [Abstract] [Full Text] [Related]

  • 11. Activator-independent functions of the yeast mediator sin4 complex in preinitiation complex formation and transcription reinitiation.
    Reeves WM, Hahn S.
    Mol Cell Biol; 2003 Jan; 23(1):349-58. PubMed ID: 12482986
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Dissecting the regulatory circuitry of a eukaryotic genome.
    Holstege FC, Jennings EG, Wyrick JJ, Lee TI, Hengartner CJ, Green MR, Golub TR, Lander ES, Young RA.
    Cell; 1998 Nov 25; 95(5):717-28. PubMed ID: 9845373
    [Abstract] [Full Text] [Related]

  • 14. Mutual targeting of mediator and the TFIIH kinase Kin28.
    Guidi BW, Bjornsdottir G, Hopkins DC, Lacomis L, Erdjument-Bromage H, Tempst P, Myers LC.
    J Biol Chem; 2004 Jul 09; 279(28):29114-20. PubMed ID: 15126497
    [Abstract] [Full Text] [Related]

  • 15. EWS, but not EWS-FLI-1, is associated with both TFIID and RNA polymerase II: interactions between two members of the TET family, EWS and hTAFII68, and subunits of TFIID and RNA polymerase II complexes.
    Bertolotti A, Melot T, Acker J, Vigneron M, Delattre O, Tora L.
    Mol Cell Biol; 1998 Mar 09; 18(3):1489-97. PubMed ID: 9488465
    [Abstract] [Full Text] [Related]

  • 16. 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 09; 22(21):7365-71. PubMed ID: 12370284
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Sfl1 functions via the co-repressor Ssn6-Tup1 and the cAMP-dependent protein kinase Tpk2.
    Conlan RS, Tzamarias D.
    J Mol Biol; 2001 Jun 22; 309(5):1007-15. PubMed ID: 11399075
    [Abstract] [Full Text] [Related]

  • 19. Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns.
    Kirschner DB, vom Baur E, Thibault C, Sanders SL, Gangloff YG, Davidson I, Weil PA, Tora L.
    Mol Cell Biol; 2002 May 22; 22(9):3178-93. PubMed ID: 11940675
    [Abstract] [Full Text] [Related]

  • 20. Transcriptional activation by yeast PDR1p is inhibited by its association with NGG1p/ADA3p.
    Martens JA, Genereaux J, Saleh A, Brandl CJ.
    J Biol Chem; 1996 Jul 05; 271(27):15884-90. PubMed ID: 8663102
    [Abstract] [Full Text] [Related]

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