HDAC1 acetylation is linked to progressive modulation of steroid receptor-induced gene transcription (Q24292915)

positive regulation of transcription by RNA polymerase II

GOA release 2020-03-11

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GOA release 2020-03-11

Malgorzata Wiench

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Gordon L. Hager

object named as

Gordon L Hager

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Diana Stavreva

object named as

Diana A Stavreva

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author name string

Yi Qiu

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Yingming Zhao

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Matthias Becker

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Sam John

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Bhavin S Parekh

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Suming Huang

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Anindya Hendarwanto

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Elisabeth D Martinez

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Yue Chen

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Hanxin Lu

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Nicholas L Adkins

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Philippe T Georgel

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R Louis Schiltz

Regulation of histone deacetylase activities

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language of work or name

English

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publication date

9 June 2006

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669-79

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cites work

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Individual histone deacetylases in Drosophila modulate transcription of distinct genes.

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Coactivator and corepressor complexes in nuclear receptor function

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Transcriptional repression by nuclear hormone receptors

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Histone hyperacetylation does not alter the positioning or stability of phased nucleosomes on the mouse mammary tumor virus long terminal repeat

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Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

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Inhibition of MMTV transcription by HDAC inhibitors occurs independent of changes in chromatin remodeling and increased histone acetylation

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Multiple mechanisms induce transcriptional silencing of a subset of genes, including oestrogen receptor alpha, in response to deacetylase inhibition by valproic acid and trichostatin A.

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Transcriptional state of the mouse mammary tumor virus promoter can affect topological domain size in vivo

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SUMO-1 modification of histone deacetylase 1 (HDAC1) modulates its biological activities

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Two regions of the mouse mammary tumor virus long terminal repeat regulate the activity of its promoter in mammary cell lines

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Butyrate and trichostatin A effects on the proliferation/differentiation of human intestinal epithelial cells: induction of cyclin D3 and p21 expression

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