326 related articles for article (PubMed ID: 25446993)
21. 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]
22. 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]
23. Change in post-translational modifications of histone H3, heat-shock protein-27 and MAP kinase p38 expression by curcumin in streptozotocin-induced type I diabetic nephropathy.
Tikoo K; Meena RL; Kabra DG; Gaikwad AB
Br J Pharmacol; 2008 Mar; 153(6):1225-31. PubMed ID: 18204486
[TBL] [Abstract][Full Text] [Related]
24. p300-mediated histone acetylation is essential for the regulation of GATA4 and MEF2C by BMP2 in H9c2 cells.
Zheng M; Zhu J; Lu T; Liu L; Sun H; Liu Z; Tian J
Cardiovasc Toxicol; 2013 Dec; 13(4):316-22. PubMed ID: 23632743
[TBL] [Abstract][Full Text] [Related]
25. Curcumin-mediated cardiac defects in mouse is associated with a reduced histone H3 acetylation and reduced expression of cardiac transcription factors.
Sun H; Zhu J; Lu T; Huang X; Tian J
Cardiovasc Toxicol; 2014 Jun; 14(2):162-9. PubMed ID: 24323078
[TBL] [Abstract][Full Text] [Related]
26. p300/CBP acetyl transferases interact with and acetylate the nucleotide excision repair factor XPG.
Tillhon M; Cazzalini O; Nardo T; Necchi D; Sommatis S; Stivala LA; Scovassi AI; Prosperi E
DNA Repair (Amst); 2012 Oct; 11(10):844-52. PubMed ID: 22954786
[TBL] [Abstract][Full Text] [Related]
27. Curcumin analogue C66 attenuates obesity-induced renal injury by inhibiting chronic inflammation.
Ye L; Hu X; Hu X; Yin S; Chen J; He H; Hong S; Yang B; Singh KK; Feng J; Wang Y; Luo W; Liang G
Biomed Pharmacother; 2021 May; 137():111418. PubMed ID: 33761621
[TBL] [Abstract][Full Text] [Related]
28. Curcumin-induced histone hypoacetylation: the role of reactive oxygen species.
Kang J; Chen J; Shi Y; Jia J; Zhang Y
Biochem Pharmacol; 2005 Apr; 69(8):1205-13. PubMed ID: 15794941
[TBL] [Abstract][Full Text] [Related]
29. C-peptide prevents NF-κB from recruiting p300 and binding to the inos promoter in diabetic nephropathy.
Li Y; Li X; He K; Li B; Liu K; Qi J; Wang H; Wang Y; Luo W
FASEB J; 2018 Apr; 32(4):2269-2279. PubMed ID: 29229684
[TBL] [Abstract][Full Text] [Related]
30. Sp1, acetylated histone-3 and p300 regulate TRAIL transcription: mechanisms of PDGF-BB-mediated VSMC proliferation and migration.
Azahri NS; Di Bartolo BA; Khachigian LM; Kavurma MM
J Cell Biochem; 2012 Aug; 113(8):2597-606. PubMed ID: 22415975
[TBL] [Abstract][Full Text] [Related]
31. Curcumin analogue C66 ameliorates mouse cardiac dysfunction and structural disorders after acute myocardial infarction via suppressing JNK activation.
Hao H; Yuan T; Li Z; Zhang C; Liu J; Liang G; Feng L; Pan Y
Eur J Pharmacol; 2023 May; 946():175629. PubMed ID: 36868294
[TBL] [Abstract][Full Text] [Related]
32. Critical role of histone acetylation by p300 in human placental 11β-HSD2 expression.
Li J; Wang W; Liu C; Wang W; Li W; Shu Q; Chen ZJ; Sun K
J Clin Endocrinol Metab; 2013 Jul; 98(7):E1189-97. PubMed ID: 23714681
[TBL] [Abstract][Full Text] [Related]
33. JNK signaling-dependent regulation of histone acetylation are involved in anacardic acid alleviates cardiomyocyte hypertrophy induced by phenylephrine.
Peng B; Peng C; Luo X; Wu S; Mao Q; Zhang H; Han X
PLoS One; 2021; 16(12):e0261388. PubMed ID: 34914791
[TBL] [Abstract][Full Text] [Related]
34. The role of p300 histone acetyltransferase in UV-induced histone modifications and MMP-1 gene transcription.
Kim MK; Shin JM; Eun HC; Chung JH
PLoS One; 2009; 4(3):e4864. PubMed ID: 19287485
[TBL] [Abstract][Full Text] [Related]
35. [Relationship between histone acetylation modification in spleen CD4+T cells and diabetic nephropathy of nonobese diabetic mice].
Hou C; Ouyang L; Wang Y; Zhou Z
Zhonghua Yi Xue Za Zhi; 2015 Apr; 95(14):1061-5. PubMed ID: 26081204
[TBL] [Abstract][Full Text] [Related]
36. RNA Binding to CBP Stimulates Histone Acetylation and Transcription.
Bose DA; Donahue G; Reinberg D; Shiekhattar R; Bonasio R; Berger SL
Cell; 2017 Jan; 168(1-2):135-149.e22. PubMed ID: 28086087
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Inhibitor of CBP Histone Acetyltransferase Downregulates p53 Activation and Facilitates Methylation at Lysine 27 on Histone H3.
Vincek AS; Patel J; Jaganathan A; Green A; Pierre-Louis V; Arora V; Rehmann J; Mezei M; Zhou MM; Ohlmeyer M; Mujtaba S
Molecules; 2018 Aug; 23(8):. PubMed ID: 30072621
[TBL] [Abstract][Full Text] [Related]
39. Curcumin prevents diabetes-associated abnormalities in the kidneys by inhibiting p300 and nuclear factor-kappaB.
Chiu J; Khan ZA; Farhangkhoee H; Chakrabarti S
Nutrition; 2009 Sep; 25(9):964-72. PubMed ID: 19268536
[TBL] [Abstract][Full Text] [Related]
40. Histone acetylation by CBP and p300 at double-strand break sites facilitates SWI/SNF chromatin remodeling and the recruitment of non-homologous end joining factors.
Ogiwara H; Ui A; Otsuka A; Satoh H; Yokomi I; Nakajima S; Yasui A; Yokota J; Kohno T
Oncogene; 2011 May; 30(18):2135-46. PubMed ID: 21217779
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
