Mechanism of corepressor binding and release from nuclear hormone receptors. - Wikidata - awgldk - TriplyDB

Mechanism of corepressor binding and release from nuclear hormone receptors.

Mechanism of corepressor binding and release from nuclear hormone receptors.

http://www.wikidata.org/entity/Q35210560

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9-cis-13,14-Dihydroretinoic Acid Is an Endogenous Retinoid Acting as RXR Ligand in Mice Evolution of a novel subfamily of nuclear receptors with members that each contain two DNA binding domains Receptor-interacting protein 140 directly recruits histone deacetylases for gene silencing A novel nuclear receptor corepressor complex, N-CoR, contains components of the mammalian SWI/SNF complex and the corepressor KAP-1 CIA, a novel estrogen receptor coactivator with a bifunctional nuclear receptor interacting determinant A transcriptional corepressor of Stat1 with an essential LXXLL signature motif Synergy between estrogen receptor alpha activation functions AF1 and AF2 mediated by transcription intermediary factor TIF2.RAP80, a novel nuclear protein that interacts with the retinoid-related testis-associated receptor Regulation of nuclear receptor transcriptional activity by a novel DEAD box RNA helicase (DP97)The peroxisome proliferator-activated receptor delta, an integrator of transcriptional repression and nuclear receptor signaling.Signaling disrupts mSin3A binding to the Mad1-like Sin3-interacting domain of TIEG2, an Sp1-like repressor Corepressors: custom tailoring and alterations while you wait.Nuclear receptor corepressors Ligand-specific allosteric regulation of coactivator functions of androgen receptor in prostate cancer cells Arsenic trioxide is a potent inhibitor of the interaction of SMRT corepressor with Its transcription factor partners, including the PML-retinoic acid receptor alpha oncoprotein found in human acute promyelocytic leukemia Oligomerization of ETO is obligatory for corepressor interaction Orphan nuclear receptor TLX recruits histone deacetylases to repress transcription and regulate neural stem cell proliferation The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor Sharp, an inducible cofactor that integrates nuclear receptor repression and activation SMRT repression of nuclear receptors controls the adipogenic set point and metabolic homeostasis The repressor DREAM acts as a transcriptional activator on Vitamin D and retinoic acid response elements Nuclear receptor corepressors and PPARgamma The structural basis for the specificity of retinoid-X receptor-selective agonists: new insights into the role of helix H12 Structural basis for antagonist-mediated recruitment of nuclear co-repressors by PPARalpha Identification of a potent synthetic FXR agonist with an unexpected mode of binding and activation Structure of Rev-erbα bound to N-CoR reveals a unique mechanism of nuclear receptor–co-repressor interaction Structural basis for a molecular allosteric control mechanism of cofactor binding to nuclear receptors Nuclear receptor Rev-erbalpha: a heme receptor that coordinates circadian rhythm and metabolism Identification of a novel testicular orphan receptor-4 (TR4)-associated protein as repressor for the selective suppression of TR4-mediated transactivation T:G mismatch-specific thymine-DNA glycosylase potentiates transcription of estrogen-regulated genes through direct interaction with estrogen receptor alpha Distinct effects of PIAS proteins on androgen-mediated gene activation in prostate cancer cells RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding The SMRT corepressor is a target of phosphorylation by protein kinase CK2 (casein kinase II)Corepressors selectively control the transcriptional activity of PPARgamma in adipocytes The nuclear corepressor, NCoR, regulates thyroid hormone action in vivo The histone-binding code of nuclear receptor co-repressors matches the substrate specificity of histone deacetylase 3 Ligand-dependent formation of retinoid receptors, receptor-interacting protein 140 (RIP140), and histone deacetylase complex is mediated by a novel receptor-interacting motif of RIP140 Isolation and characterization of mammalian HDAC10, a novel histone deacetylase Core LXXLL motif sequences in CREB-binding protein, SRC1, and RIP140 define affinity and selectivity for steroid and retinoid receptors.Mass-spectrometric analysis of agonist-induced retinoic acid receptor gamma conformational change.

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Mechanism of corepressor binding and release from nuclear hormone receptors.

http://www.wikidata.org/entity/Q35210560

description

1999 nî lūn-bûn

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1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1999年の論文

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1999年論文

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1999年論文

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1999年論文

@zh-hk

1999年論文

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1999年論文

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1999年论文

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name

Mechanism of corepressor binding and release from nuclear hormone receptors.

@ast

Mechanism of corepressor binding and release from nuclear hormone receptors.

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type

label

Mechanism of corepressor binding and release from nuclear hormone receptors.

@ast

Mechanism of corepressor binding and release from nuclear hormone receptors.

@en

prefLabel

Mechanism of corepressor binding and release from nuclear hormone receptors.

@ast

Mechanism of corepressor binding and release from nuclear hormone receptors.

@en

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Genes & Development

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Mechanism of corepressor binding and release from nuclear hormone receptors

@en

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C Li

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E Banayo

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H Y Kao

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J D Love

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J T Gooch

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K Chatterjee

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L Nagy

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V Krishna

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P2860

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

Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex

Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300

Two receptor interaction domains in the corepressor, N-CoR/RIP13, are required for an efficient interaction with Rev-erbA alpha and RVR: physical association is dependent on the E region of the orphan receptors

GRIP1, a novel mouse protein that serves as a transcriptional coactivator in yeast for the hormone binding domains of steroid receptors

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

Structure and specificity of nuclear receptor-coactivator interactions

The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen

Sequence and characterization of a coactivator for the steroid hormone receptor superfamily

A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors

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3209-3216

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scholarly article

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10.1101/GAD.13.24.3209

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24

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13

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Ronald M. Evans

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1999-12-01T00:00:00Z

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51363237

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10617570

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317208

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