BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 9753545)

  • 1. TOM1p, a yeast hect-domain protein which mediates transcriptional regulation through the ADA/SAGA coactivator complexes.
    Saleh A; Collart M; Martens JA; Genereaux J; Allard S; Cote J; Brandl CJ
    J Mol Biol; 1998 Oct; 282(5):933-46. PubMed ID: 9753545
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 22(21):7365-71. PubMed ID: 12370284
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inhibition of TATA-binding protein function by SAGA subunits Spt3 and Spt8 at Gcn4-activated promoters.
    Belotserkovskaya R; Sterner DE; Deng M; Sayre MH; Lieberman PM; Berger SL
    Mol Cell Biol; 2000 Jan; 20(2):634-47. PubMed ID: 10611242
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GCN5, a yeast transcriptional coactivator, induces chromatin reconfiguration of HIS3 promoter in vivo.
    Filetici P; Aranda C; Gonzàlez A; Ballario P
    Biochem Biophys Res Commun; 1998 Jan; 242(1):84-7. PubMed ID: 9439614
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Components of the SAGA histone acetyltransferase complex are required for repressed transcription of ARG1 in rich medium.
    Ricci AR; Genereaux J; Brandl CJ
    Mol Cell Biol; 2002 Jun; 22(12):4033-42. PubMed ID: 12024017
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of distinct yeast Not2 functional domains with components of Gcn5 histone acetylase and Ccr4 transcriptional regulatory complexes.
    Benson JD; Benson M; Howley PM; Struhl K
    EMBO J; 1998 Nov; 17(22):6714-22. PubMed ID: 9822614
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The S. cerevisiae SAGA complex functions in vivo as a coactivator for transcriptional activation by Gal4.
    Larschan E; Winston F
    Genes Dev; 2001 Aug; 15(15):1946-56. PubMed ID: 11485989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preferential accessibility of the yeast his3 promoter is determined by a general property of the DNA sequence, not by specific elements.
    Mai X; Chou S; Struhl K
    Mol Cell Biol; 2000 Sep; 20(18):6668-76. PubMed ID: 10958664
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo.
    Kuo MH; Zhou J; Jambeck P; Churchill ME; Allis CD
    Genes Dev; 1998 Mar; 12(5):627-39. PubMed ID: 9499399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SAGA is an essential in vivo target of the yeast acidic activator Gal4p.
    Bhaumik SR; Green MR
    Genes Dev; 2001 Aug; 15(15):1935-45. PubMed ID: 11485988
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Critical residues for histone acetylation by Gcn5, functioning in Ada and SAGA complexes, are also required for transcriptional function in vivo.
    Wang L; Liu L; Berger SL
    Genes Dev; 1998 Mar; 12(5):640-53. PubMed ID: 9499400
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transcription. Proteasome parts at gene promoters.
    Ottosen S; Herrera FJ; Triezenberg SJ
    Science; 2002 Apr; 296(5567):479-81. PubMed ID: 11964465
    [No Abstract]   [Full Text] [Related]  

  • 14. 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; 21(5):1101-11. PubMed ID: 11867538
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recruitment of chromatin remodelling factors during gene activation via the glucocorticoid receptor N-terminal domain.
    Wallberg AE; Flinn EM; Gustafsson JA; Wright AP
    Biochem Soc Trans; 2000; 28(4):410-4. PubMed ID: 10961930
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The E2 ubiquitin conjugase Rad6 is required for the ArgR/Mcm1 repression of ARG1 transcription.
    Turner SD; Ricci AR; Petropoulos H; Genereaux J; Skerjanc IS; Brandl CJ
    Mol Cell Biol; 2002 Jun; 22(12):4011-9. PubMed ID: 12024015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extragenic suppressors that rescue defects in the heat stress response of the budding yeast mutant tom1.
    Sasaki T; Toh-e A; Kikuchi Y
    Mol Gen Genet; 2000 Jan; 262(6):940-8. PubMed ID: 10660055
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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(9):1411-22. PubMed ID: 11857084
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation.
    Grant PA; Schieltz D; Pray-Grant MG; Steger DJ; Reese JC; Yates JR; Workman JL
    Cell; 1998 Jul; 94(1):45-53. PubMed ID: 9674426
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recruitment of HAT complexes by direct activator interactions with the ATM-related Tra1 subunit.
    Brown CE; Howe L; Sousa K; Alley SC; Carrozza MJ; Tan S; Workman JL
    Science; 2001 Jun; 292(5525):2333-7. PubMed ID: 11423663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.