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Similar articles for PubMed (Select 21742760)


Histone modifications influence mediator interactions with chromatin.

Zhu X, Zhang Y, Bjornsdottir G, Liu Z, Quan A, Costanzo M, Dávila López M, Westholm JO, Ronne H, Boone C, Gustafsson CM, Myers LC.

Nucleic Acids Res. 2011 Oct;39(19):8342-54. doi: 10.1093/nar/gkr551. Epub 2011 Jul 8.


Med5(Nut1) and Med17(Srb4) are direct targets of mediator histone H4 tail interactions.

Liu Z, Myers LC.

PLoS One. 2012;7(6):e38416. doi: 10.1371/journal.pone.0038416. Epub 2012 Jun 5.


Efficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation pattern.

Braunstein M, Sobel RE, Allis CD, Turner BM, Broach JR.

Mol Cell Biol. 1996 Aug;16(8):4349-56.


NuA4 links methylation of histone H3 lysines 4 and 36 to acetylation of histones H4 and H3.

Ginsburg DS, Anlembom TE, Wang J, Patel SR, Li B, Hinnebusch AG.

J Biol Chem. 2014 Nov 21;289(47):32656-70. doi: 10.1074/jbc.M114.585588. Epub 2014 Oct 9.


In vivo effects of histone H3 depletion on nucleosome occupancy and position in Saccharomyces cerevisiae.

Gossett AJ, Lieb JD.

PLoS Genet. 2012;8(6):e1002771. doi: 10.1371/journal.pgen.1002771. Epub 2012 Jun 21.


Regulation of NuA4 histone acetyltransferase activity in transcription and DNA repair by phosphorylation of histone H4.

Utley RT, Lacoste N, Jobin-Robitaille O, Allard S, Côté J.

Mol Cell Biol. 2005 Sep;25(18):8179-90.


Nuclear matrix, dynamic histone acetylation and transcriptionally active chromatin.

Davie JR.

Mol Biol Rep. 1997 Aug;24(3):197-207. Review.


Combined action of PHD and chromo domains directs the Rpd3S HDAC to transcribed chromatin.

Li B, Gogol M, Carey M, Lee D, Seidel C, Workman JL.

Science. 2007 May 18;316(5827):1050-4.


Splitting of H3-H4 tetramers at transcriptionally active genes undergoing dynamic histone exchange.

Katan-Khaykovich Y, Struhl K.

Proc Natl Acad Sci U S A. 2011 Jan 25;108(4):1296-301. doi: 10.1073/pnas.1018308108. Epub 2011 Jan 10.


The tail-module of yeast Mediator complex is required for telomere heterochromatin maintenance.

Peng J, Zhou JQ.

Nucleic Acids Res. 2012 Jan;40(2):581-93. doi: 10.1093/nar/gkr757. Epub 2011 Sep 19.


Differential contributions of histone H3 and H4 residues to heterochromatin structure.

Yu Q, Olsen L, Zhang X, Boeke JD, Bi X.

Genetics. 2011 Jun;188(2):291-308. doi: 10.1534/genetics.111.127886. Epub 2011 Mar 24.


Selective recognition of acetylated histones by bromodomains in transcriptional co-activators.

Hassan AH, Awad S, Al-Natour Z, Othman S, Mustafa F, Rizvi TA.

Biochem J. 2007 Feb 15;402(1):125-33.


Comprehensive structural analysis of mutant nucleosomes containing lysine to glutamine (KQ) substitutions in the H3 and H4 histone-fold domains.

Iwasaki W, Tachiwana H, Kawaguchi K, Shibata T, Kagawa W, Kurumizaka H.

Biochemistry. 2011 Sep 13;50(36):7822-32. doi: 10.1021/bi201021h. Epub 2011 Aug 17.


Histone H4 lysine 91 acetylation a core domain modification associated with chromatin assembly.

Ye J, Ai X, Eugeni EE, Zhang L, Carpenter LR, Jelinek MA, Freitas MA, Parthun MR.

Mol Cell. 2005 Apr 1;18(1):123-30.


Genome-wide integration on transcription factors, histone acetylation and gene expression reveals genes co-regulated by histone modification patterns.

Natsume-Kitatani Y, Shiga M, Mamitsuka H.

PLoS One. 2011;6(7):e22281. doi: 10.1371/journal.pone.0022281. Epub 2011 Jul 29.


Histone H3K4 and K36 methylation, Chd1 and Rpd3S oppose the functions of Saccharomyces cerevisiae Spt4-Spt5 in transcription.

Quan TK, Hartzog GA.

Genetics. 2010 Feb;184(2):321-34. doi: 10.1534/genetics.109.111526. Epub 2009 Nov 30.


Elongator is a histone H3 and H4 acetyltransferase important for normal histone acetylation levels in vivo.

Winkler GS, Kristjuhan A, Erdjument-Bromage H, Tempst P, Svejstrup JQ.

Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3517-22.

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