(Q33826663)

29 July 2017

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title

Transcriptional repression by nuclear hormone receptors (English)

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29 July 2017

Hu X

1

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29 July 2017

Lazar MA

series ordinal

2

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29 July 2017

publication date

1 January 2000

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Trends in Endocrinology and Metabolism

29 July 2017

published in

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29 July 2017

volume

11

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29 July 2017

issue

1

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29 July 2017

page(s)

6-10

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The nuclear receptor superfamily: the second decade

29 July 2017

cites work

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A transcriptional co-repressor that interacts with nuclear hormone receptors

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SMRTe, a silencing mediator for retinoid and thyroid hormone receptors-extended isoform that is more related to the nuclear receptor corepressor

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SMRTER, a Drosophila nuclear receptor coregulator, reveals that EcR-mediated repression is critical for development.

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A nuclear hormone receptor corepressor mediates transcriptional silencing by receptors with distinct repression domains.

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Two receptor interacting domains in the nuclear hormone receptor corepressor RIP13/N-CoR

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Transcriptional silencing is defined by isoform- and heterodimer-specific interactions between nuclear hormone receptors and corepressors

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The CoRNR motif controls the recruitment of corepressors by nuclear hormone receptors

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The nuclear receptor ligand-binding domain: structure and function

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7 January 2021

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7 January 2021

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7 January 2021

A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

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29 July 2017

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