Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB. (Q33779119)

29 July 2017

title

Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB. (English)

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29 July 2017

C W Wong

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29 July 2017

M L Privalsky

series ordinal

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29 July 2017

language of work or name

English

0 references

publication date

1 September 1998

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Molecular and Cellular Biology

29 July 2017

published in

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

5500-5510

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The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70.

29 July 2017

cites work

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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The tau 4 activation domain of the thyroid hormone receptor is required for release of a putative corepressor(s) necessary for transcriptional silencing

4 July 2018

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4 July 2018

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A transcriptional co-repressor that interacts with nuclear hormone receptors

4 July 2018

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4 July 2018

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Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor

4 July 2018

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RPD3 encodes a second factor required to achieve maximum positive and negative transcriptional states in Saccharomyces cerevisiae

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Protein encoded by v-erbA functions as a thyroid-hormone receptor antagonist

30 October 2018

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12 December 2020

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Stoichiometric and steric principles governing repression by nuclear hormone receptors

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Identifiers

DOI

10.1128/MCB.18.9.5500

1 reference

29 July 2017

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29 July 2017

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