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4. Enhancers are activated by p300/CBP activity-dependent PIC assembly, RNAPII recruitment, and pause release. Narita T; Ito S; Higashijima Y; Chu WK; Neumann K; Walter J; Satpathy S; Liebner T; Hamilton WB; Maskey E; Prus G; Shibata M; Iesmantavicius V; Brickman JM; Anastassiadis K; Koseki H; Choudhary C Mol Cell; 2021 May; 81(10):2166-2182.e6. PubMed ID: 33765415 [TBL] [Abstract][Full Text] [Related]
5. Histone Acetyltransferase p300 Induces De Novo Super-Enhancers to Drive Cellular Senescence. Sen P; Lan Y; Li CY; Sidoli S; Donahue G; Dou Z; Frederick B; Chen Q; Luense LJ; Garcia BA; Dang W; Johnson FB; Adams PD; Schultz DC; Berger SL Mol Cell; 2019 Feb; 73(4):684-698.e8. PubMed ID: 30773298 [TBL] [Abstract][Full Text] [Related]
6. The histone acetyltransferase activity of PCAF cooperates with the brahma/SWI2-related protein BRG-1 in the activation of the enhancer A of the MHC class I promoter. Brockmann D; Lehmkühler O; Schmücker U; Esche H Gene; 2001 Oct; 277(1-2):111-20. PubMed ID: 11602348 [TBL] [Abstract][Full Text] [Related]
7. Loci-specific histone acetylation profiles associated with transcriptional coactivator p300 during early myoblast differentiation. Khilji S; Hamed M; Chen J; Li Q Epigenetics; 2018; 13(6):642-654. PubMed ID: 29927685 [TBL] [Abstract][Full Text] [Related]
8. Targeting histone acetylation dynamics and oncogenic transcription by catalytic P300/CBP inhibition. Hogg SJ; Motorna O; Cluse LA; Johanson TM; Coughlan HD; Raviram R; Myers RM; Costacurta M; Todorovski I; Pijpers L; Bjelosevic S; Williams T; Huskins SN; Kearney CJ; Devlin JR; Fan Z; Jabbari JS; Martin BP; Fareh M; Kelly MJ; Dupéré-Richer D; Sandow JJ; Feran B; Knight D; Khong T; Spencer A; Harrison SJ; Gregory G; Wickramasinghe VO; Webb AI; Taberlay PC; Bromberg KD; Lai A; Papenfuss AT; Smyth GK; Allan RS; Licht JD; Landau DA; Abdel-Wahab O; Shortt J; Vervoort SJ; Johnstone RW Mol Cell; 2021 May; 81(10):2183-2200.e13. PubMed ID: 34019788 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Differential contribution of p300 and CBP to regulatory element acetylation in mESCs. Martire S; Nguyen J; Sundaresan A; Banaszynski LA BMC Mol Cell Biol; 2020 Jul; 21(1):55. PubMed ID: 32690000 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. DUX4 recruits p300/CBP through its C-terminus and induces global H3K27 acetylation changes. Choi SH; Gearhart MD; Cui Z; Bosnakovski D; Kim M; Schennum N; Kyba M Nucleic Acids Res; 2016 Jun; 44(11):5161-73. PubMed ID: 26951377 [TBL] [Abstract][Full Text] [Related]
13. The human proliferating Cell nuclear antigen regulates transcriptional coactivator p300 activity and promotes transcriptional repression. Hong R; Chakravarti D J Biol Chem; 2003 Nov; 278(45):44505-13. PubMed ID: 12937166 [TBL] [Abstract][Full Text] [Related]
14. Time-Resolved Analysis Reveals Rapid Dynamics and Broad Scope of the CBP/p300 Acetylome. Weinert BT; Narita T; Satpathy S; Srinivasan B; Hansen BK; Schölz C; Hamilton WB; Zucconi BE; Wang WW; Liu WR; Brickman JM; Kesicki EA; Lai A; Bromberg KD; Cole PA; Choudhary C Cell; 2018 Jun; 174(1):231-244.e12. PubMed ID: 29804834 [TBL] [Abstract][Full Text] [Related]
15. Lysine acetyltransferases cyclic adenosine monophosphate response element-binding binding protein and acetyltransferase p300 attenuate transcriptional activity of the mineralocorticoid receptor through its acetylation. Seo M; Song M; Seok YM; Kang SH; Lee HA; Sohn UD; Kim IK Clin Exp Pharmacol Physiol; 2015 May; 42(5):559-66. PubMed ID: 25707758 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Roles of coactivators in hypoxic induction of the erythropoietin gene. Wang F; Zhang R; Wu X; Hankinson O PLoS One; 2010 Apr; 5(4):e10002. PubMed ID: 20368990 [TBL] [Abstract][Full Text] [Related]
18. The pioneer factor activity of c-Myb involves recruitment of p300 and induction of histone acetylation followed by acetylation-induced chromatin dissociation. Fuglerud BM; Ledsaak M; Rogne M; Eskeland R; Gabrielsen OS Epigenetics Chromatin; 2018 Jun; 11(1):35. PubMed ID: 29954426 [TBL] [Abstract][Full Text] [Related]
19. Acetylation of histone H2B marks active enhancers and predicts CBP/p300 target genes. Narita T; Higashijima Y; Kilic S; Liebner T; Walter J; Choudhary C Nat Genet; 2023 Apr; 55(4):679-692. PubMed ID: 37024579 [TBL] [Abstract][Full Text] [Related]
20. Is histone acetylation the most important physiological function for CBP and p300? Bedford DC; Brindle PK Aging (Albany NY); 2012 Apr; 4(4):247-55. PubMed ID: 22511639 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]