(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

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29 July 2017

Lazar MA

series ordinal

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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

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29 July 2017

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

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A transcriptional co-repressor that interacts with nuclear hormone receptors

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A histone deacetylase corepressor complex regulates the Notch signal transduction pathway

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Unique forms of human and mouse nuclear receptor corepressor SMRT

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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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Alien, a highly conserved protein with characteristics of a corepressor for members of the nuclear hormone receptor superfamily

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Cloning and characterization of a corepressor and potential component of the nuclear hormone receptor repression complex

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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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7 January 2021

Stoichiometric and steric principles governing repression by nuclear hormone receptors

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7 January 2021

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

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7 January 2021

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

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7 January 2021

The nuclear receptor ligand-binding domain: structure and function

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Ligand binding and co-activator assembly of the peroxisome proliferator-activated receptor-gamma

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7 January 2021

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7 January 2021

Differential recognition of liganded and unliganded thyroid hormone receptor by retinoid X receptor regulates transcriptional repression

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7 January 2021

Crystal structure of the ligand-binding domain of the human nuclear receptor RXR-alpha

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Transcriptional Activation and Repression by ROR , an Orphan Nuclear Receptor Required for Cerebellar Development

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The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR or SMRT

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7 January 2021

Coactivator and corepressor regulation of the agonist/antagonist activity of the mixed antiestrogen, 4-hydroxytamoxifen.

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An estrogen receptor-selective coregulator that potentiates the effectiveness of antiestrogens and represses the activity of estrogens

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7 January 2021

A novel role for helix 12 of retinoid X receptor in regulating repression

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7 January 2021

Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression

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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

Nuclear receptor repression mediated by a complex containing SMRT, mSin3A, and histone deacetylase

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7 January 2021

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

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7 January 2021

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7 January 2021

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7 January 2021

Signaling by tyrosine kinases negatively regulates the interaction between transcription factors and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) corepressor

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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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7 January 2021

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Identifiers

DOI

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29 July 2017

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