Nuclear histone acetylases and deacetylases and transcriptional regulation: HATs off to HDACs.
暂无分享,去创建一个
[1] D. Reinberg,et al. Histone Deacetylases and SAP18, a Novel Polypeptide, Are Components of a Human Sin3 Complex , 1997, Cell.
[2] Wen‐Ming Yang,et al. Histone Deacetylases Associated with the mSin3 Corepressor Mediate Mad Transcriptional Repression , 1997, Cell.
[3] S. Schreiber,et al. Nuclear Receptor Repression Mediated by a Complex Containing SMRT, mSin3A, and Histone Deacetylase , 1997, Cell.
[4] K. Struhl,et al. Repression by Ume6 Involves Recruitment of a Complex Containing Sin3 Corepressor and Rpd3 Histone Deacetylase to Target Promoters , 1997, Cell.
[5] Stuart L Schreiber,et al. Histone Deacetylase Activity Is Required for Full Transcriptional Repression by mSin3A , 1997, Cell.
[6] M. Pazin,et al. What's Up and Down with Histone Deacetylation and Transcription? , 1997, Cell.
[7] A. Wolffe. Sinful repression , 1997, nature.
[8] L. Chin,et al. Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression , 1997, nature.
[9] C. Glass,et al. A complex containing N-CoR, mSln3 and histone deacetylase mediates transcriptional repression , 1997, nature.
[10] C. Glass,et al. Peroxisome proliferator-activated receptors and retinoic acid receptors differentially control the interactions of retinoid X receptor heterodimers with ligands, coactivators, and corepressors , 1997, Molecular and cellular biology.
[11] Andrew J. Bannister,et al. The TAFII250 Subunit of TFIID Has Histone Acetyltransferase Activity , 1996, Cell.
[12] K. Struhl,et al. The histone deacetylase RPD3 counteracts genomic silencing in Drosophila and yeast , 1996, Nature.
[13] M. Grunstein,et al. HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[14] B. Howard,et al. The Transcriptional Coactivators p300 and CBP Are Histone Acetyltransferases , 1996, Cell.
[15] D M Schmatz,et al. Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[16] Wen‐Ming Yang,et al. Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[17] C. Allis,et al. Histone Acetylation and Chromatin Assembly: A Single Escort, Multiple Dances? , 1996, Cell.
[18] Jonathan Widom,et al. The Major Cytoplasmic Histone Acetyltransferase in Yeast: Links to Chromatin Replication and Histone Metabolism , 1996, Cell.
[19] R. Kobayashi,et al. Nucleosome Assembly by a Complex of CAF-1 and Acetylated Histones H3/H4 , 1996, Cell.
[20] C. Allis,et al. Transcription-linked acetylation by Gcn5p of histones H3 and H4 at specific lysines , 1996, Nature.
[21] T. Hunter,et al. A growing coactivator network , 1996, Nature.
[22] B M Turner,et al. Efficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation pattern , 1996, Molecular and cellular biology.
[23] B. Howard,et al. A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A , 1996, Nature.
[24] M. Vettese-Dadey,et al. Acetylation of histone H4 plays a primary role in enhancing transcription factor binding to nucleosomal DNA in vitro. , 1996, The EMBO journal.
[25] A. Wolffe,et al. Histone Deacetylase--A Regulator of Transcription , 1996, Science.
[26] S. Schreiber,et al. A Mammalian Histone Deacetylase Related to the Yeast Transcriptional Regulator Rpd3p , 1996, Science.
[27] C. Allis,et al. Special HATs for special occasions: linking histone acetylation to chromatin assembly and gene activation. , 1996, Current opinion in genetics & development.
[28] C. Allis,et al. Tetrahymena Histone Acetyltransferase A: A Homolog to Yeast Gcn5p Linking Histone Acetylation to Gene Activation , 1996, Cell.
[29] S. Berger,et al. Structural and Functional Analysis of Yeast Putative Adaptors , 1996, The Journal of Biological Chemistry.
[30] D. Shore,et al. Suppressors of defective silencing in yeast: effects on transcriptional repression at the HMR locus, cell growth and telomere structure. , 1995, Genetics.
[31] J. Walton,et al. Inhibition of maize histone deacetylases by HC toxin, the host-selective toxin of Cochliobolus carbonum. , 1995, The Plant cell.
[32] R. Sternglanz,et al. Identification of a Gene Encoding a Yeast Histone H4 Acetyltransferase (*) , 1995, The Journal of Biological Chemistry.
[33] B. Turner,et al. Histone H4 acetylation distinguishes coding regions of the human genome from heterochromatin in a differentiation‐dependent but transcription‐independent manner. , 1995, The EMBO journal.
[34] R. Bernards. Transcriptional Regulation: Flipping the Myc switch , 1995, Current Biology.
[35] E. Moran,et al. Relief of YY1 transcriptional repression by adenovirus E1A is mediated by E1A-associated protein p300. , 1995, Genes & development.
[36] S. Horinouchi,et al. Trichostatin A and trapoxin: Novel chemical probes for the role of histone acetylation in chromatin structure and function , 1995, BioEssays : news and reviews in molecular, cellular and developmental biology.
[37] R. Eisenman,et al. Mad-max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3 , 1995, Cell.
[38] L. Chin,et al. An amino-terminal domain of Mxi1 mediates anti-myc oncogenic activity and interacts with a homolog of the Yeast Transcriptional Repressor SIN3 , 1995, Cell.
[39] C. Allis,et al. Conservation of deposition-related acetylation sites in newly synthesized histones H3 and H4. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[40] D. Wechsler,et al. Differential binding of c-Myc and Max to nucleosomal DNA. , 1994, Molecular and cellular biology.
[41] S. Dorland,et al. Epistasis analysis of suppressor mutations that allow HO expression in the absence of the yeast SW15 transcriptional activator. , 1994, Genetics.
[42] M. Yoshida,et al. Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase. , 1993, The Journal of biological chemistry.
[43] B. Turner. Decoding the nucleosome , 1993, Cell.
[44] B. Turner,et al. The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression , 1993, Cell.
[45] A. Mitchell,et al. Bipartite structure of an early meiotic upstream activation sequence from Saccharomyces cerevisiae , 1993, Molecular and cellular biology.
[46] Alan P. Wolffe,et al. A positive role for histone acetylation in transcription factor access to nucleosomal DNA , 1993, Cell.
[47] M. Grunstein,et al. Histone H3 N‐terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo. , 1992, The EMBO journal.
[48] B. Turner,et al. Histone H4 isoforms acetylated at specific lysine residues define individual chromosomes and chromatin domains in Drosophila polytene nuclei , 1992, Cell.
[49] K. Sugita,et al. A Novel Tetracyclic Peptide, Trapoxin, Induces Phenotypic Change from Transformed to Normal in sis‐Oncogene‐transformed NIH3T3 Cells , 1992, Japanese journal of cancer research : Gann.
[50] M. Vidal,et al. RPD3 encodes a second factor required to achieve maximum positive and negative transcriptional states in Saccharomyces cerevisiae , 1991, Molecular and cellular biology.
[51] M. Grunstein,et al. Yeast histone H4 N-terminal sequence is required for promoter activation in vivo , 1991, Cell.
[52] M. Yoshida,et al. Reversible arrest of proliferation of rat 3Y1 fibroblasts in both the G1 and G2 phases by trichostatin A. , 1988, Experimental cell research.
[53] D. Rich,et al. Analogues of the cytostatic and antimitogenic agents chlamydocin and HC-toxin: synthesis and biological activity of chloromethyl ketone and diazomethyl ketone functionalized cyclic tetrapeptides. , 1987, Journal of medicinal chemistry.
[54] V. Allfrey,et al. Studies of acetylation and deacetylation in high mobility group proteins. Identification of the sites of acetylation in high mobility group proteins 14 and 17. , 1981, The Journal of biological chemistry.
[55] V. Ingram,et al. n-Butyrate causes histone modification in HeLa and Friend erythroleukaemia cells , 1977, Nature.
[56] M. Kuroda,et al. Acetylated histone H4 on the male X chromosome is associated with dosage compensation in Drosophila. , 1994, Genes & development.