319 related articles for article (PubMed ID: 21774670)
1. Regulation of insulin gene transcription by multiple histone acetyltransferases.
Sampley ML; Ozcan S
DNA Cell Biol; 2012 Jan; 31(1):8-14. PubMed ID: 21774670
[TBL] [Abstract][Full Text] [Related]
2. Distinct roles of GCN5/PCAF-mediated H3K9ac and CBP/p300-mediated H3K18/27ac in nuclear receptor transactivation.
Jin Q; Yu LR; Wang L; Zhang Z; Kasper LH; Lee JE; Wang C; Brindle PK; Dent SY; Ge K
EMBO J; 2011 Jan; 30(2):249-62. PubMed ID: 21131905
[TBL] [Abstract][Full Text] [Related]
3. Glucose regulation of insulin gene expression requires the recruitment of p300 by the beta-cell-specific transcription factor Pdx-1.
Mosley AL; Corbett JA; Ozcan S
Mol Endocrinol; 2004 Sep; 18(9):2279-90. PubMed ID: 15166251
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. CBP/p300 double null cells reveal effect of coactivator level and diversity on CREB transactivation.
Kasper LH; Lerach S; Wang J; Wu S; Jeevan T; Brindle PK
EMBO J; 2010 Nov; 29(21):3660-72. PubMed ID: 20859256
[TBL] [Abstract][Full Text] [Related]
9. Differential Effects of Histone Acetyltransferase GCN5 or PCAF Knockdown on Urothelial Carcinoma Cells.
Koutsogiannouli EA; Wagner N; Hader C; Pinkerneil M; Hoffmann MJ; Schulz WA
Int J Mol Sci; 2017 Jul; 18(7):. PubMed ID: 28678170
[TBL] [Abstract][Full Text] [Related]
10. Involvement of p300/CBP and epigenetic histone acetylation in TGF-β1-mediated gene transcription in mesangial cells.
Yuan H; Reddy MA; Sun G; Lanting L; Wang M; Kato M; Natarajan R
Am J Physiol Renal Physiol; 2013 Mar; 304(5):F601-13. PubMed ID: 23235480
[TBL] [Abstract][Full Text] [Related]
11. The HSP90 molecular chaperone cycle regulates cyclical transcriptional dynamics of the glucocorticoid receptor and its coregulatory molecules CBP/p300 during ultradian ligand treatment.
Conway-Campbell BL; George CL; Pooley JR; Knight DM; Norman MR; Hager GL; Lightman SL
Mol Endocrinol; 2011 Jun; 25(6):944-54. PubMed ID: 21511880
[TBL] [Abstract][Full Text] [Related]
12. Distinct embryonic expression and localization of CBP and p300 histone acetyltransferases at the mouse alphaA-crystallin locus in lens.
Yang Y; Wolf LV; Cvekl A
J Mol Biol; 2007 Jun; 369(4):917-26. PubMed ID: 17467007
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Glucose regulates insulin gene transcription by hyperacetylation of histone h4.
Mosley AL; Ozcan S
J Biol Chem; 2003 May; 278(22):19660-6. PubMed ID: 12665509
[TBL] [Abstract][Full Text] [Related]
17. 5-Fluorouracil targets histone acetyltransferases p300/CBP in the treatment of colorectal cancer.
Du C; Huang D; Peng Y; Yao Y; Zhao Y; Yang Y; Wang H; Cao L; Zhu WG; Gu J
Cancer Lett; 2017 Aug; 400():183-193. PubMed ID: 28465257
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Trichostatin A induces transforming growth factor beta type II receptor promoter activity and acetylation of Sp1 by recruitment of PCAF/p300 to a Sp1.NF-Y complex.
Huang W; Zhao S; Ammanamanchi S; Brattain M; Venkatasubbarao K; Freeman JW
J Biol Chem; 2005 Mar; 280(11):10047-54. PubMed ID: 15647279
[TBL] [Abstract][Full Text] [Related]
20. Dynamic histone acetylation/deacetylation with progesterone receptor-mediated transcription.
Aoyagi S; Archer TK
Mol Endocrinol; 2007 Apr; 21(4):843-56. PubMed ID: 17227884
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
