882 related articles for article (PubMed ID: 21131905)
41. 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]
42. CBP and p300 histone acetyltransferases contribute to homologous recombination by transcriptionally activating the BRCA1 and RAD51 genes.
Ogiwara H; Kohno T
PLoS One; 2012; 7(12):e52810. PubMed ID: 23285190
[TBL] [Abstract][Full Text] [Related]
43. Acetyltransferase p300/CBP associated Factor (PCAF) regulates crosstalk-dependent acetylation of histone H3 by distal site recognition.
Kornacki JR; Stuparu AD; Mrksich M
ACS Chem Biol; 2015 Jan; 10(1):157-64. PubMed ID: 25203060
[TBL] [Abstract][Full Text] [Related]
44. Recruitment of nuclear factor Y to the inverted CCAAT element (ICE) by c-Jun and E1A stimulates basal transcription of the bone sialoprotein gene in osteosarcoma cells.
Su M; Bansal AK; Mantovani R; Sodek J
J Biol Chem; 2005 Nov; 280(46):38365-75. PubMed ID: 16087680
[TBL] [Abstract][Full Text] [Related]
45. The histone acetyltransferase activity of human GCN5 and PCAF is stabilized by coenzymes.
Herrera JE; Bergel M; Yang XJ; Nakatani Y; Bustin M
J Biol Chem; 1997 Oct; 272(43):27253-8. PubMed ID: 9341171
[TBL] [Abstract][Full Text] [Related]
46. Application of a fluorescent histone acetyltransferase assay to probe the substrate specificity of the human p300/CBP-associated factor.
Trievel RC; Li FY; Marmorstein R
Anal Biochem; 2000 Dec; 287(2):319-28. PubMed ID: 11112280
[TBL] [Abstract][Full Text] [Related]
47. Upregulation of OATP1A2 in human oesophageal squamous cell carcinoma cells via the HDAC6-GCN5/PCAF-H3K9Ac axis.
Zheng X; Zhang JV; Bai Y; Wang J; Jiang M; Zeng S; Wang L
Xenobiotica; 2021 Dec; 51(12):1453-1462. PubMed ID: 34823432
[TBL] [Abstract][Full Text] [Related]
48. Stimulation of DNA replication from the polyomavirus origin by PCAF and GCN5 acetyltransferases: acetylation of large T antigen.
Xie AY; Bermudez VP; Folk WR
Mol Cell Biol; 2002 Nov; 22(22):7907-18. PubMed ID: 12391158
[TBL] [Abstract][Full Text] [Related]
49. A viral mechanism for inhibition of p300 and PCAF acetyltransferase activity.
Chakravarti D; Ogryzko V; Kao HY; Nash A; Chen H; Nakatani Y; Evans RM
Cell; 1999 Feb; 96(3):393-403. PubMed ID: 10025405
[TBL] [Abstract][Full Text] [Related]
50. Genome-wide and single-cell analyses reveal a context dependent relationship between CBP recruitment and gene expression.
Kasper LH; Qu C; Obenauer JC; McGoldrick DJ; Brindle PK
Nucleic Acids Res; 2014 Oct; 42(18):11363-82. PubMed ID: 25249627
[TBL] [Abstract][Full Text] [Related]
51. Histone acetyltransferase promotes fluoride toxicity in LS8 cells.
Deng H; Fujiwara N; Cui H; Whitford GM; Bartlett JD; Suzuki M
Chemosphere; 2020 May; 247():125825. PubMed ID: 31927229
[TBL] [Abstract][Full Text] [Related]
52. Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation.
Peng GH; Chen S
Hum Mol Genet; 2007 Oct; 16(20):2433-52. PubMed ID: 17656371
[TBL] [Abstract][Full Text] [Related]
53. HIPK2 contributes to PCAF-mediated p53 acetylation and selective transactivation of p21Waf1 after nonapoptotic DNA damage.
Di Stefano V; Soddu S; Sacchi A; D'Orazi G
Oncogene; 2005 Aug; 24(35):5431-42. PubMed ID: 15897882
[TBL] [Abstract][Full Text] [Related]
54. Coordination of a transcriptional switch by HMGI(Y) acetylation.
Munshi N; Agalioti T; Lomvardas S; Merika M; Chen G; Thanos D
Science; 2001 Aug; 293(5532):1133-6. PubMed ID: 11498590
[TBL] [Abstract][Full Text] [Related]
55. Transcriptional activation of human matrix metalloproteinase-9 gene expression by multiple co-activators.
Zhao X; Benveniste EN
J Mol Biol; 2008 Nov; 383(5):945-56. PubMed ID: 18790699
[TBL] [Abstract][Full Text] [Related]
56. CBP/p300 is a cell type-specific modulator of CLOCK/BMAL1-mediated transcription.
Hosoda H; Kato K; Asano H; Ito M; Kato H; Iwamoto T; Suzuki A; Masushige S; Kida S
Mol Brain; 2009 Nov; 2():34. PubMed ID: 19922678
[TBL] [Abstract][Full Text] [Related]
57. Dynamic acetylation of all lysine-4 trimethylated histone H3 is evolutionarily conserved and mediated by p300/CBP.
Crump NT; Hazzalin CA; Bowers EM; Alani RM; Cole PA; Mahadevan LC
Proc Natl Acad Sci U S A; 2011 May; 108(19):7814-9. PubMed ID: 21518915
[TBL] [Abstract][Full Text] [Related]
58. The metazoan ATAC and SAGA coactivator HAT complexes regulate different sets of inducible target genes.
Nagy Z; Riss A; Fujiyama S; Krebs A; Orpinell M; Jansen P; Cohen A; Stunnenberg HG; Kato S; Tora L
Cell Mol Life Sci; 2010 Feb; 67(4):611-28. PubMed ID: 19936620
[TBL] [Abstract][Full Text] [Related]
59. Non-histone protein acetylation by the evolutionarily conserved GCN5 and PCAF acetyltransferases.
Downey M
Biochim Biophys Acta Gene Regul Mech; 2021 Feb; 1864(2):194608. PubMed ID: 32711095
[TBL] [Abstract][Full Text] [Related]
60. IL-1β-specific recruitment of GCN5 histone acetyltransferase induces the release of PAF1 from chromatin for the de-repression of inflammatory response genes.
Kim N; Sun HY; Youn MY; Yoo JY
Nucleic Acids Res; 2013 Apr; 41(8):4495-506. PubMed ID: 23502002
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
