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Results: 1 to 20 of 157

Similar articles for PubMed (Select 23804093)

1.

A novel activator of CBP/p300 acetyltransferases promotes neurogenesis and extends memory duration in adult mice.

Chatterjee S, Mizar P, Cassel R, Neidl R, Selvi BR, Mohankrishna DV, Vedamurthy BM, Schneider A, Bousiges O, Mathis C, Cassel JC, Eswaramoorthy M, Kundu TK, Boutillier AL.

J Neurosci. 2013 Jun 26;33(26):10698-712. doi: 10.1523/JNEUROSCI.5772-12.2013.

2.

E2A proteins enhance the histone acetyltransferase activity of the transcriptional co-activators CBP and p300.

Hyndman BD, Thompson P, Bayly R, Côté GP, LeBrun DP.

Biochim Biophys Acta. 2012 May;1819(5):446-53. doi: 10.1016/j.bbagrm.2012.02.009. Epub 2012 Feb 22.

PMID:
22387215
3.

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. doi: 10.1038/npp.2010.117. Epub 2010 Sep 1.

4.

Regulation of insulin gene transcription by multiple histone acetyltransferases.

Sampley ML, Ozcan S.

DNA Cell Biol. 2012 Jan;31(1):8-14. doi: 10.1089/dna.2011.1336. Epub 2011 Jul 20.

5.

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.

7.
8.

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. doi: 10.1371/journal.pone.0052810. Epub 2012 Dec 20.

9.

Dynamic acetylation of all lysine-4 trimethylated histone H3 is evolutionarily conserved and mediated by p300/CBP.

Crump NT, Hazzalin CA, Bowers EM, Alani RM, Cole PA, Mahadevan LC.

Proc Natl Acad Sci U S A. 2011 May 10;108(19):7814-9. doi: 10.1073/pnas.1100099108. Epub 2011 Apr 25.

10.

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 3;29(21):3660-72. doi: 10.1038/emboj.2010.235. Epub 2010 Sep 21.

11.

Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity.

Giralt A, Puigdellívol M, Carretón O, Paoletti P, Valero J, Parra-Damas A, Saura CA, Alberch J, Ginés S.

Hum Mol Genet. 2012 Mar 15;21(6):1203-16. doi: 10.1093/hmg/ddr552. Epub 2011 Nov 24.

12.

Ablation of CBP in forebrain principal neurons causes modest memory and transcriptional defects and a dramatic reduction of histone acetylation but does not affect cell viability.

Valor LM, Pulopulos MM, Jimenez-Minchan M, Olivares R, Lutz B, Barco A.

J Neurosci. 2011 Feb 2;31(5):1652-63. doi: 10.1523/JNEUROSCI.4737-10.2011.

13.

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.

14.

CREB-binding protein/p300 co-activation of crystallin gene expression.

Chen Q, Dowhan DH, Liang D, Moore DD, Overbeek PA.

J Biol Chem. 2002 Jul 5;277(27):24081-9. Epub 2002 Apr 9.

15.

Critical loss of CBP/p300 histone acetylase activity by caspase-6 during neurodegeneration.

Rouaux C, Jokic N, Mbebi C, Boutillier S, Loeffler JP, Boutillier AL.

EMBO J. 2003 Dec 15;22(24):6537-49.

16.

Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders.

Valor LM, Viosca J, Lopez-Atalaya JP, Barco A.

Curr Pharm Des. 2013;19(28):5051-64. Review.

17.

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 Jun 13;8(6):e66076. doi: 10.1371/journal.pone.0066076. Print 2013.

18.

The transcriptional regulator CBP has defined spatial associations within interphase nuclei.

McManus KJ, Stephens DA, Adams NM, Islam SA, Freemont PS, Hendzel MJ.

PLoS Comput Biol. 2006 Oct 20;2(10):e139. Epub 2006 Sep 8.

19.

CBP histone acetyltransferase activity is a critical component of memory consolidation.

Korzus E, Rosenfeld MG, Mayford M.

Neuron. 2004 Jun 24;42(6):961-72.

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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