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Items: 1 to 20 of 159

1.

Interaction between acetylated MyoD and the bromodomain of CBP and/or p300.

Polesskaya A, Naguibneva I, Duquet A, Bengal E, Robin P, Harel-Bellan A.

Mol Cell Biol. 2001 Aug;21(16):5312-20.

2.

CREB-binding protein/p300 activates MyoD by acetylation.

Polesskaya A, Duquet A, Naguibneva I, Weise C, Vervisch A, Bengal E, Hucho F, Robin P, Harel-Bellan A.

J Biol Chem. 2000 Nov 3;275(44):34359-64.

3.
4.

Acetylation of MyoD by p300 requires more than its histone acetyltransferase domain.

Polesskaya A, Harel-Bellan A.

J Biol Chem. 2001 Nov 30;276(48):44502-3. Epub 2001 Sep 27.

5.

Differential role of p300 and CBP acetyltransferase during myogenesis: p300 acts upstream of MyoD and Myf5.

Roth JF, Shikama N, Henzen C, Desbaillets I, Lutz W, Marino S, Wittwer J, Schorle H, Gassmann M, Eckner R.

EMBO J. 2003 Oct 1;22(19):5186-96.

6.
7.

Acetylation of beta-catenin by p300 regulates beta-catenin-Tcf4 interaction.

Lévy L, Wei Y, Labalette C, Wu Y, Renard CA, Buendia MA, Neuveut C.

Mol Cell Biol. 2004 Apr;24(8):3404-14.

8.

Mechanisms of P/CAF auto-acetylation.

Santos-Rosa H, Valls E, Kouzarides T, Martínez-Balbás M.

Nucleic Acids Res. 2003 Aug 1;31(15):4285-92.

9.

Regulation of E2F1 activity by acetylation.

Martínez-Balbás MA, Bauer UM, Nielsen SJ, Brehm A, Kouzarides T.

EMBO J. 2000 Feb 15;19(4):662-71.

10.

MyoD stimulates RB promoter activity via the CREB/p300 nuclear transduction pathway.

Magenta A, Cenciarelli C, De Santa F, Fuschi P, Martelli F, Caruso M, Felsani A.

Mol Cell Biol. 2003 Apr;23(8):2893-906.

11.

Differential roles of p300 and PCAF acetyltransferases in muscle differentiation.

Puri PL, Sartorelli V, Yang XJ, Hamamori Y, Ogryzko VV, Howard BH, Kedes L, Wang JY, Graessmann A, Nakatani Y, Levrero M.

Mol Cell. 1997 Dec;1(1):35-45.

12.

Acetylation of importin-alpha nuclear import factors by CBP/p300.

Bannister AJ, Miska EA, Görlich D, Kouzarides T.

Curr Biol. 2000 Apr 20;10(8):467-70.

14.

In vitro transcription system delineates the distinct roles of the coactivators pCAF and p300 during MyoD/E47-dependent transactivation.

Dilworth FJ, Seaver KJ, Fishburn AL, Htet SL, Tapscott SJ.

Proc Natl Acad Sci U S A. 2004 Aug 10;101(32):11593-8. Epub 2004 Aug 2.

15.

Differential binding modes of the bromodomains of CREB-binding protein (CBP) and p300 with acetylated MyoD.

Wei L, Jamonnak N, Choy J, Wang Z, Zheng W.

Biochem Biophys Res Commun. 2008 Apr 4;368(2):279-84. doi: 10.1016/j.bbrc.2008.01.071. Epub 2008 Jan 28.

17.

p53 sites acetylated in vitro by PCAF and p300 are acetylated in vivo in response to DNA damage.

Liu L, Scolnick DM, Trievel RC, Zhang HB, Marmorstein R, Halazonetis TD, Berger SL.

Mol Cell Biol. 1999 Feb;19(2):1202-9.

18.

The histone acetyltransferase, hGCN5, interacts with and acetylates the HIV transactivator, Tat.

Col E, Caron C, Seigneurin-Berny D, Gracia J, Favier A, Khochbin S.

J Biol Chem. 2001 Jul 27;276(30):28179-84. Epub 2001 May 30.

19.

Acetylation by histone acetyltransferase CREB-binding protein/p300 of STAT6 is required for transcriptional activation of the 15-lipoxygenase-1 gene.

Shankaranarayanan P, Chaitidis P, Kühn H, Nigam S.

J Biol Chem. 2001 Nov 16;276(46):42753-60. Epub 2001 Aug 16.

20.

The transcriptional coactivators p300 and CBP are histone acetyltransferases.

Ogryzko VV, Schiltz RL, Russanova V, Howard BH, Nakatani Y.

Cell. 1996 Nov 29;87(5):953-9.

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