503 related articles for article (PubMed ID: 9697775)
1. Transcriptional activators direct histone acetyltransferase complexes to nucleosomes.
Utley RT; Ikeda K; Grant PA; Côté J; Steger DJ; Eberharter A; John S; Workman JL
Nature; 1998 Jul; 394(6692):498-502. PubMed ID: 9697775
[TBL] [Abstract][Full Text] [Related]
2. Identification and analysis of yeast nucleosomal histone acetyltransferase complexes.
Eberharter A; John S; Grant PA; Utley RT; Workman JL
Methods; 1998 Aug; 15(4):315-21. PubMed ID: 9740719
[TBL] [Abstract][Full Text] [Related]
3. p300-mediated acetylation facilitates the transfer of histone H2A-H2B dimers from nucleosomes to a histone chaperone.
Ito T; Ikehara T; Nakagawa T; Kraus WL; Muramatsu M
Genes Dev; 2000 Aug; 14(15):1899-907. PubMed ID: 10921904
[TBL] [Abstract][Full Text] [Related]
4. Distribution of acetylated histones resulting from Gal4-VP16 recruitment of SAGA and NuA4 complexes.
Vignali M; Steger DJ; Neely KE; Workman JL
EMBO J; 2000 Jun; 19(11):2629-40. PubMed ID: 10835360
[TBL] [Abstract][Full Text] [Related]
5. GCN5 dependence of chromatin remodeling and transcriptional activation by the GAL4 and VP16 activation domains in budding yeast.
Stafford GA; Morse RH
Mol Cell Biol; 2001 Jul; 21(14):4568-78. PubMed ID: 11416135
[TBL] [Abstract][Full Text] [Related]
6. Histone acetyltransferase activity and interaction with ADA2 are critical for GCN5 function in vivo.
Candau R; Zhou JX; Allis CD; Berger SL
EMBO J; 1997 Feb; 16(3):555-65. PubMed ID: 9034338
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. Distinct GCN5/PCAF-containing complexes function as co-activators and are involved in transcription factor and global histone acetylation.
Nagy Z; Tora L
Oncogene; 2007 Aug; 26(37):5341-57. PubMed ID: 17694077
[TBL] [Abstract][Full Text] [Related]
12. Steroid receptor coactivator-1 is a histone acetyltransferase.
Spencer TE; Jenster G; Burcin MM; Allis CD; Zhou J; Mizzen CA; McKenna NJ; Onate SA; Tsai SY; Tsai MJ; O'Malley BW
Nature; 1997 Sep; 389(6647):194-8. PubMed ID: 9296499
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Snf1--a histone kinase that works in concert with the histone acetyltransferase Gcn5 to regulate transcription.
Lo WS; Duggan L; Emre NC; Belotserkovskya R; Lane WS; Shiekhattar R; Berger SL
Science; 2001 Aug; 293(5532):1142-6. PubMed ID: 11498592
[TBL] [Abstract][Full Text] [Related]
15. The CBP co-activator is a histone acetyltransferase.
Bannister AJ; Kouzarides T
Nature; 1996 Dec 19-26; 384(6610):641-3. PubMed ID: 8967953
[TBL] [Abstract][Full Text] [Related]
16. Remodeling chromatin structures for transcription: what happens to the histones?
Steger DJ; Workman JL
Bioessays; 1996 Nov; 18(11):875-84. PubMed ID: 8939065
[TBL] [Abstract][Full Text] [Related]
17. Evidence for distinct mechanisms facilitating transcript elongation through chromatin in vivo.
Kristjuhan A; Svejstrup JQ
EMBO J; 2004 Oct; 23(21):4243-52. PubMed ID: 15457216
[TBL] [Abstract][Full Text] [Related]
18. The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.
Sudarsanam P; Cao Y; Wu L; Laurent BC; Winston F
EMBO J; 1999 Jun; 18(11):3101-6. PubMed ID: 10357821
[TBL] [Abstract][Full Text] [Related]
19. Histone acetyltransferase activity is conserved between yeast and human GCN5 and is required for complementation of growth and transcriptional activation.
Wang L; Mizzen C; Ying C; Candau R; Barlev N; Brownell J; Allis CD; Berger SL
Mol Cell Biol; 1997 Jan; 17(1):519-27. PubMed ID: 8972232
[TBL] [Abstract][Full Text] [Related]
20. Histone H3 specific acetyltransferases are essential for cell cycle progression.
Howe L; Auston D; Grant P; John S; Cook RG; Workman JL; Pillus L
Genes Dev; 2001 Dec; 15(23):3144-54. PubMed ID: 11731478
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
