BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

464 related articles for article (PubMed ID: 9674426)

  • 1. 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]  

  • 2. Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex.
    Grant PA; Duggan L; Côté J; Roberts SM; Brownell JE; Candau R; Ohba R; Owen-Hughes T; Allis CD; Winston F; Berger SL; Workman JL
    Genes Dev; 1997 Jul; 11(13):1640-50. PubMed ID: 9224714
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The TAF(II)250 subunit of TFIID has histone acetyltransferase activity.
    Mizzen CA; Yang XJ; Kokubo T; Brownell JE; Bannister AJ; Owen-Hughes T; Workman J; Wang L; Berger SL; Kouzarides T; Nakatani Y; Allis CD
    Cell; 1996 Dec; 87(7):1261-70. PubMed ID: 8980232
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Redundant roles for the TFIID and SAGA complexes in global transcription.
    Lee TI; Causton HC; Holstege FC; Shen WC; Hannett N; Jennings EG; Winston F; Green MR; Young RA
    Nature; 2000 Jun; 405(6787):701-4. PubMed ID: 10864329
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Role of the Ada2 and Ada3 transcriptional coactivators in histone acetylation.
    Balasubramanian R; Pray-Grant MG; Selleck W; Grant PA; Tan S
    J Biol Chem; 2002 Mar; 277(10):7989-95. PubMed ID: 11773077
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. IFN-Stimulated transcription through a TBP-free acetyltransferase complex escapes viral shutoff.
    Paulson M; Press C; Smith E; Tanese N; Levy DE
    Nat Cell Biol; 2002 Feb; 4(2):140-7. PubMed ID: 11802163
    [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. The ADA complex is a distinct histone acetyltransferase complex in Saccharomyces cerevisiae.
    Eberharter A; Sterner DE; Schieltz D; Hassan A; Yates JR; Berger SL; Workman JL
    Mol Cell Biol; 1999 Oct; 19(10):6621-31. PubMed ID: 10490601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Gcn5 bromodomain co-ordinates nucleosome remodelling.
    Syntichaki P; Topalidou I; Thireos G
    Nature; 2000 Mar; 404(6776):414-7. PubMed ID: 10746732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dissection of coactivator requirement at RNR3 reveals unexpected contributions from TFIID and SAGA.
    Zhang H; Kruk JA; Reese JC
    J Biol Chem; 2008 Oct; 283(41):27360-27368. PubMed ID: 18682387
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Post-TATA binding protein recruitment clearance of Gcn5-dependent histone acetylation within promoter nucleosomes.
    Topalidou I; Papamichos-Chronakis M; Thireos G
    Mol Cell Biol; 2003 Nov; 23(21):7809-17. PubMed ID: 14560024
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A histone fold TAF octamer within the yeast TFIID transcriptional coactivator.
    Selleck W; Howley R; Fang Q; Podolny V; Fried MG; Buratowski S; Tan S
    Nat Struct Biol; 2001 Aug; 8(8):695-700. PubMed ID: 11473260
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Gcn5.Ada complex potentiates the histone acetyltransferase activity of Gcn5.
    Syntichaki P; Thireos G
    J Biol Chem; 1998 Sep; 273(38):24414-9. PubMed ID: 9733731
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The yeast histone acetyltransferase A2 complex, but not free Gcn5p, binds stably to nucleosomal arrays.
    Sendra R; Tse C; Hansen JC
    J Biol Chem; 2000 Aug; 275(32):24928-34. PubMed ID: 10825174
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 24.