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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

459 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 23.