342 related articles for article (PubMed ID: 15715965)
1. GCN5: a supervisor in all-inclusive control of vertebrate cell cycle progression through transcription regulation of various cell cycle-related genes.
Kikuchi H; Takami Y; Nakayama T
Gene; 2005 Feb; 347(1):83-97. PubMed ID: 15715965
[TBL] [Abstract][Full Text] [Related]
2. Expression of PCAF, p300 and Gcn5 and more highly acetylated histone H4 in pediatric tumors.
Armas-Pineda C; Arenas-Huertero F; Pérezpeñia-Diazconti M; Chico-Ponce de León F; Sosa-Sáinz G; Lezama P; Recillas-Targa F
J Exp Clin Cancer Res; 2007 Jun; 26(2):269-76. PubMed ID: 17725108
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. HiNF-D (CDP-cut/CDC2/cyclin A/pRB-complex) influences the timing of IRF-2-dependent cell cycle activation of human histone H4 gene transcription at the G1/S phase transition.
Aziz F; van Wijnen AJ; Stein JL; Stein GS
J Cell Physiol; 1998 Dec; 177(3):453-64. PubMed ID: 9808153
[TBL] [Abstract][Full Text] [Related]
6. CBP/p300 histone acetyl-transferase activity is important for the G1/S transition.
Ait-Si-Ali S; Polesskaya A; Filleur S; Ferreira R; Duquet A; Robin P; Vervish A; Trouche D; Cabon F; Harel-Bellan A
Oncogene; 2000 May; 19(20):2430-7. PubMed ID: 10828885
[TBL] [Abstract][Full Text] [Related]
7. Human papillomavirus type 16 E7 protein increases acetylation of histone H3 in human foreskin keratinocytes.
Zhang B; Laribee RN; Klemsz MJ; Roman A
Virology; 2004 Nov; 329(1):189-98. PubMed ID: 15476886
[TBL] [Abstract][Full Text] [Related]
8. Down-regulation of p300/CBP histone acetyltransferase activates a senescence checkpoint in human melanocytes.
Bandyopadhyay D; Okan NA; Bales E; Nascimento L; Cole PA; Medrano EE
Cancer Res; 2002 Nov; 62(21):6231-9. PubMed ID: 12414652
[TBL] [Abstract][Full Text] [Related]
9. GCN5 regulates the superoxide-generating system in leukocytes via controlling gp91-phox gene expression.
Kikuchi H; Kuribayashi F; Kiwaki N; Takami Y; Nakayama T
J Immunol; 2011 Mar; 186(5):3015-22. PubMed ID: 21278346
[TBL] [Abstract][Full Text] [Related]
10. A mechanism for coordinating chromatin modification and preinitiation complex assembly.
Black JC; Choi JE; Lombardo SR; Carey M
Mol Cell; 2006 Sep; 23(6):809-18. PubMed ID: 16973433
[TBL] [Abstract][Full Text] [Related]
11. Human histone acetyltransferase GCN5 exists in a stable macromolecular complex lacking the adapter ADA2.
Forsberg EC; Lam LT; Yang XJ; Nakatani Y; Bresnick EH
Biochemistry; 1997 Dec; 36(50):15918-24. PubMed ID: 9398325
[TBL] [Abstract][Full Text] [Related]
12. GCN5 and p300 share essential functions during early embryogenesis.
Phan HM; Xu AW; Coco C; Srajer G; Wyszomierski S; Evrard YA; Eckner R; Dent SY
Dev Dyn; 2005 Aug; 233(4):1337-47. PubMed ID: 15937931
[TBL] [Abstract][Full Text] [Related]
13. Distinct but overlapping roles of histone acetylase PCAF and of the closely related PCAF-B/GCN5 in mouse embryogenesis.
Yamauchi T; Yamauchi J; Kuwata T; Tamura T; Yamashita T; Bae N; Westphal H; Ozato K; Nakatani Y
Proc Natl Acad Sci U S A; 2000 Oct; 97(21):11303-6. PubMed ID: 11027331
[TBL] [Abstract][Full Text] [Related]
14. A conserved central region of yeast Ada2 regulates the histone acetyltransferase activity of Gcn5 and interacts with phospholipids.
Hoke SM; Genereaux J; Liang G; Brandl CJ
J Mol Biol; 2008 Dec; 384(4):743-55. PubMed ID: 18950642
[TBL] [Abstract][Full Text] [Related]
15. E2F-dependent histone acetylation and recruitment of the Tip60 acetyltransferase complex to chromatin in late G1.
Taubert S; Gorrini C; Frank SR; Parisi T; Fuchs M; Chan HM; Livingston DM; Amati B
Mol Cell Biol; 2004 May; 24(10):4546-56. PubMed ID: 15121871
[TBL] [Abstract][Full Text] [Related]
16. Loss of Gcn5l2 leads to increased apoptosis and mesodermal defects during mouse development.
Xu W; Edmondson DG; Evrard YA; Wakamiya M; Behringer RR; Roth SY
Nat Genet; 2000 Oct; 26(2):229-32. PubMed ID: 11017084
[TBL] [Abstract][Full Text] [Related]
17. Epigenetic control of ovarian function: the emerging role of histone modifications.
LaVoie HA
Mol Cell Endocrinol; 2005 Nov; 243(1-2):12-8. PubMed ID: 16219412
[TBL] [Abstract][Full Text] [Related]
18. Gene profiling of cell cycle progression through S-phase reveals sequential expression of genes required for DNA replication and nucleosome assembly.
van der Meijden CM; Lapointe DS; Luong MX; Peric-Hupkes D; Cho B; Stein JL; van Wijnen AJ; Stein GS
Cancer Res; 2002 Jun; 62(11):3233-43. PubMed ID: 12036939
[TBL] [Abstract][Full Text] [Related]
19. P300 plays a role in p16(INK4a) expression and cell cycle arrest.
Wang X; Pan L; Feng Y; Wang Y; Han Q; Han L; Han S; Guo J; Huang B; Lu J
Oncogene; 2008 Mar; 27(13):1894-904. PubMed ID: 17906698
[TBL] [Abstract][Full Text] [Related]
20. H4 acetylation does not replace H3 acetylation in chromatin remodelling and transcription activation of Adr1-dependent genes.
Agricola E; Verdone L; Di Mauro E; Caserta M
Mol Microbiol; 2006 Dec; 62(5):1433-46. PubMed ID: 17121596
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
