483 related articles for article (PubMed ID: 22511639)
21. Structure-activity relationship and antitumor activity of 1,4-pyrazine-containing inhibitors of histone acetyltransferases P300/CBP.
Nie S; Wu F; Wu J; Li X; Zhou C; Yao Y; Song Y
Eur J Med Chem; 2022 Jul; 237():114407. PubMed ID: 35512565
[TBL] [Abstract][Full Text] [Related]
22. Histone Acetyltransferases p300 and CBP Coordinate Distinct Chromatin Remodeling Programs in Vascular Smooth Muscle Plasticity.
Chakraborty R; Ostriker AC; Xie Y; Dave JM; Gamez-Mendez A; Chatterjee P; Abu Y; Valentine J; Lezon-Geyda K; Greif DM; Schulz VP; Gallagher PG; Sessa WC; Hwa J; Martin KA
Circulation; 2022 Jun; 145(23):1720-1737. PubMed ID: 35502657
[TBL] [Abstract][Full Text] [Related]
23. Dual regulation of c-Myc by p300 via acetylation-dependent control of Myc protein turnover and coactivation of Myc-induced transcription.
Faiola F; Liu X; Lo S; Pan S; Zhang K; Lymar E; Farina A; Martinez E
Mol Cell Biol; 2005 Dec; 25(23):10220-34. PubMed ID: 16287840
[TBL] [Abstract][Full Text] [Related]
24. Histone deacetylase inhibitors synergize p300 autoacetylation that regulates its transactivation activity and complex formation.
Stiehl DP; Fath DM; Liang D; Jiang Y; Sang N
Cancer Res; 2007 Mar; 67(5):2256-2264. PubMed ID: 17332356
[TBL] [Abstract][Full Text] [Related]
25. Histone acetylation by p300 is involved in CREB-mediated transcription on chromatin.
Yuan LW; Gambee JE
Biochim Biophys Acta; 2001 Dec; 1541(3):161-9. PubMed ID: 11755210
[TBL] [Abstract][Full Text] [Related]
26. Structure and chemistry of the p300/CBP and Rtt109 histone acetyltransferases: implications for histone acetyltransferase evolution and function.
Wang L; Tang Y; Cole PA; Marmorstein R
Curr Opin Struct Biol; 2008 Dec; 18(6):741-7. PubMed ID: 18845255
[TBL] [Abstract][Full Text] [Related]
27. Spatial memory consolidation is associated with induction of several lysine-acetyltransferase (histone acetyltransferase) expression levels and H2B/H4 acetylation-dependent transcriptional events in the rat hippocampus.
Bousiges O; Vasconcelos AP; Neidl R; Cosquer B; Herbeaux K; Panteleeva I; Loeffler JP; Cassel JC; Boutillier AL
Neuropsychopharmacology; 2010 Dec; 35(13):2521-37. PubMed ID: 20811339
[TBL] [Abstract][Full Text] [Related]
28. Acetylation of nucleosomal histones by p300 facilitates transcription from tax-responsive human T-cell leukemia virus type 1 chromatin template.
Lu H; Pise-Masison CA; Fletcher TM; Schiltz RL; Nagaich AK; Radonovich M; Hager G; Cole PA; Brady JN
Mol Cell Biol; 2002 Jul; 22(13):4450-62. PubMed ID: 12052856
[TBL] [Abstract][Full Text] [Related]
29. Roles of HIPK1 and HIPK2 in AML1- and p300-dependent transcription, hematopoiesis and blood vessel formation.
Aikawa Y; Nguyen LA; Isono K; Takakura N; Tagata Y; Schmitz ML; Koseki H; Kitabayashi I
EMBO J; 2006 Sep; 25(17):3955-65. PubMed ID: 16917507
[TBL] [Abstract][Full Text] [Related]
30. Transcriptional deregulation of the keratin 18 gene in human colon carcinoma cells results from an altered acetylation mechanism.
Prochasson P; Delouis C; Brison O
Nucleic Acids Res; 2002 Aug; 30(15):3312-22. PubMed ID: 12140315
[TBL] [Abstract][Full Text] [Related]
31. Acetylation of HIV-1 Tat by CBP/P300 increases transcription of integrated HIV-1 genome and enhances binding to core histones.
Deng L; de la Fuente C; Fu P; Wang L; Donnelly R; Wade JD; Lambert P; Li H; Lee CG; Kashanchi F
Virology; 2000 Nov; 277(2):278-95. PubMed ID: 11080476
[TBL] [Abstract][Full Text] [Related]
32. Binding of YY1 to the proximal region of the murine beta interferon promoter is essential to allow CBP recruitment and K8H4/K14H3 acetylation on the promoter region after virus infection.
Mokrani H; Sharaf el Dein O; Mansuroglu Z; Bonnefoy E
Mol Cell Biol; 2006 Nov; 26(22):8551-61. PubMed ID: 16954376
[TBL] [Abstract][Full Text] [Related]
33. Inhibition of different histone acetyltransferases (HATs) uncovers transcription-dependent and -independent acetylation-mediated mechanisms in memory formation.
Merschbaecher K; Hatko L; Folz J; Mueller U
Learn Mem; 2016 Feb; 23(2):83-9. PubMed ID: 26773101
[TBL] [Abstract][Full Text] [Related]
34. Valproic acid exposure decreases Cbp/p300 protein expression and histone acetyltransferase activity in P19 cells.
Lamparter CL; Winn LM
Toxicol Appl Pharmacol; 2016 Sep; 306():69-78. PubMed ID: 27381264
[TBL] [Abstract][Full Text] [Related]
35. Epigenetic mechanisms to propagate histone acetylation by p300/CBP.
Kikuchi M; Morita S; Wakamori M; Sato S; Uchikubo-Kamo T; Suzuki T; Dohmae N; Shirouzu M; Umehara T
Nat Commun; 2023 Jul; 14(1):4103. PubMed ID: 37460559
[TBL] [Abstract][Full Text] [Related]
36. Influenza A virus nucleoprotein is acetylated by histone acetyltransferases PCAF and GCN5.
Hatakeyama D; Shoji M; Yamayoshi S; Yoh R; Ohmi N; Takenaka S; Saitoh A; Arakaki Y; Masuda A; Komatsu T; Nagano R; Nakano M; Noda T; Kawaoka Y; Kuzuhara T
J Biol Chem; 2018 May; 293(19):7126-7138. PubMed ID: 29555684
[TBL] [Abstract][Full Text] [Related]
37. Distinct roles for CBP and p300 on the RA-mediated expression of the meiosis commitment gene Stra8 in mouse embryonic stem cells.
Chen W; Jia W; Wang K; Si X; Zhu S; Duan T; Kang J
PLoS One; 2013; 8(6):e66076. PubMed ID: 23785470
[TBL] [Abstract][Full Text] [Related]
38. The histone acetyltransferase PCAF regulates p21 transcription through stress-induced acetylation of histone H3.
Love IM; Sekaric P; Shi D; Grossman SR; Androphy EJ
Cell Cycle; 2012 Jul; 11(13):2458-66. PubMed ID: 22713239
[TBL] [Abstract][Full Text] [Related]
39. Glucocorticoid receptor recruitment of histone deacetylase 2 inhibits interleukin-1beta-induced histone H4 acetylation on lysines 8 and 12.
Ito K; Barnes PJ; Adcock IM
Mol Cell Biol; 2000 Sep; 20(18):6891-903. PubMed ID: 10958685
[TBL] [Abstract][Full Text] [Related]
40. Transcriptional/epigenetic regulator CBP/p300 in tumorigenesis: structural and functional versatility in target recognition.
Wang F; Marshall CB; Ikura M
Cell Mol Life Sci; 2013 Nov; 70(21):3989-4008. PubMed ID: 23307074
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
