341 related articles for article (PubMed ID: 12929931)
1. P300/CBP acts as a coactivator to cartilage homeoprotein-1 (Cart1), paired-like homeoprotein, through acetylation of the conserved lysine residue adjacent to the homeodomain.
Iioka T; Furukawa K; Yamaguchi A; Shindo H; Yamashita S; Tsukazaki T
J Bone Miner Res; 2003 Aug; 18(8):1419-29. PubMed ID: 12929931
[TBL] [Abstract][Full Text] [Related]
2. Histone acetyltransferase activity of p300 is required for transcriptional repression by the promyelocytic leukemia zinc finger protein.
Guidez F; Howell L; Isalan M; Cebrat M; Alani RM; Ivins S; Hormaeche I; McConnell MJ; Pierce S; Cole PA; Licht J; Zelent A
Mol Cell Biol; 2005 Jul; 25(13):5552-66. PubMed ID: 15964811
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. p300/CREB-binding protein enhances the prolactin-mediated transcriptional induction through direct interaction with the transactivation domain of Stat5, but does not participate in the Stat5-mediated suppression of the glucocorticoid response.
Pfitzner E; Jähne R; Wissler M; Stoecklin E; Groner B
Mol Endocrinol; 1998 Oct; 12(10):1582-93. PubMed ID: 9773981
[TBL] [Abstract][Full Text] [Related]
6. Regulation of activity of the transcription factor GATA-1 by acetylation.
Boyes J; Byfield P; Nakatani Y; Ogryzko V
Nature; 1998 Dec; 396(6711):594-8. PubMed ID: 9859997
[TBL] [Abstract][Full Text] [Related]
7. The CBP bromodomain and nucleosome targeting are required for Zta-directed nucleosome acetylation and transcription activation.
Deng Z; Chen CJ; Chamberlin M; Lu F; Blobel GA; Speicher D; Cirillo LA; Zaret KS; Lieberman PM
Mol Cell Biol; 2003 Apr; 23(8):2633-44. PubMed ID: 12665567
[TBL] [Abstract][Full Text] [Related]
8. Multiple roles for acetylation in the interaction of p300 HAT with ATF-2.
Karanam B; Wang L; Wang D; Liu X; Marmorstein R; Cotter R; Cole PA
Biochemistry; 2007 Jul; 46(28):8207-16. PubMed ID: 17590016
[TBL] [Abstract][Full Text] [Related]
9. Acetylation of estrogen receptor alpha by p300 at lysines 266 and 268 enhances the deoxyribonucleic acid binding and transactivation activities of the receptor.
Kim MY; Woo EM; Chong YT; Homenko DR; Kraus WL
Mol Endocrinol; 2006 Jul; 20(7):1479-93. PubMed ID: 16497729
[TBL] [Abstract][Full Text] [Related]
10. Stimulation of CREB binding protein nucleosomal histone acetyltransferase activity by a class of transcriptional activators.
Chen CJ; Deng Z; Kim AY; Blobel GA; Lieberman PM
Mol Cell Biol; 2001 Jan; 21(2):476-87. PubMed ID: 11134336
[TBL] [Abstract][Full Text] [Related]
11. Acetylation of importin-alpha nuclear import factors by CBP/p300.
Bannister AJ; Miska EA; Görlich D; Kouzarides T
Curr Biol; 2000 Apr; 10(8):467-70. PubMed ID: 10801418
[TBL] [Abstract][Full Text] [Related]
12. Regulation of E2F1 activity by acetylation.
Martínez-Balbás MA; Bauer UM; Nielsen SJ; Brehm A; Kouzarides T
EMBO J; 2000 Feb; 19(4):662-71. PubMed ID: 10675335
[TBL] [Abstract][Full Text] [Related]
13. p300/CBP acts as a coactivator of the cone-rod homeobox transcription factor.
Yanagi Y; Masuhiro Y; Mori M; Yanagisawa J; Kato S
Biochem Biophys Res Commun; 2000 Mar; 269(2):410-4. PubMed ID: 10708567
[TBL] [Abstract][Full Text] [Related]
14. p300 functions as a transcriptional coactivator for the TAL1/SCL oncoprotein.
Huang S; Qiu Y; Stein RW; Brandt SJ
Oncogene; 1999 Sep; 18(35):4958-67. PubMed ID: 10490830
[TBL] [Abstract][Full Text] [Related]
15. Smad-dependent stimulation of type I collagen gene expression in human skin fibroblasts by TGF-beta involves functional cooperation with p300/CBP transcriptional coactivators.
Ghosh AK; Yuan W; Mori Y; Varga J
Oncogene; 2000 Jul; 19(31):3546-55. PubMed ID: 10918613
[TBL] [Abstract][Full Text] [Related]
16. CBP/p300 and associated transcriptional co-activators exhibit distinct expression patterns during murine craniofacial and neural tube development.
Bhattacherjee V; Horn KH; Singh S; Webb CL; Pisano MM; Greene RM
Int J Dev Biol; 2009; 53(7):1097-104. PubMed ID: 19598128
[TBL] [Abstract][Full Text] [Related]
17. Interactions with p300 enhance transcriptional activation by the PDZ-domain coactivator Bridge-1.
Lee JH; Volinic JL; Banz C; Yao KM; Thomas MK
J Endocrinol; 2005 Nov; 187(2):283-92. PubMed ID: 16293776
[TBL] [Abstract][Full Text] [Related]
18. The transcriptional coactivators p300 and CBP are histone acetyltransferases.
Ogryzko VV; Schiltz RL; Russanova V; Howard BH; Nakatani Y
Cell; 1996 Nov; 87(5):953-9. PubMed ID: 8945521
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Activation of Smad1-mediated transcription by p300/CBP.
Pearson KL; Hunter T; Janknecht R
Biochim Biophys Acta; 1999 Dec; 1489(2-3):354-64. PubMed ID: 10673036
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
