Activation and repression by nuclear hormone receptors: hormone modulates an equilibrium between active and repressive states.
about
CIA, a novel estrogen receptor coactivator with a bifunctional nuclear receptor interacting determinantPSF is a novel corepressor that mediates its effect through Sin3A and the DNA binding domain of nuclear hormone receptorsActivation of the orphan receptor RIP14 by retinoidsNovel mechanisms of endothelial mechanotransductionNuclear receptor Rev-erbalpha: a heme receptor that coordinates circadian rhythm and metabolismFunctional localization and competition between the androgen receptor and T-cell factor for nuclear beta-catenin: a means for inhibition of the Tcf signaling axisThe SMRT corepressor is a target of phosphorylation by protein kinase CK2 (casein kinase II)Heterodimeric interaction between retinoid X receptor alpha and orphan nuclear receptor OR1 reveals dimerization-induced activation as a novel mechanism of nuclear receptor activationThe synergistic effect of dexamethasone and all-trans-retinoic acid on hepatic phosphoenolpyruvate carboxykinase gene expression involves the coactivator p300Mechanistic principles in NR box-dependent interaction between nuclear hormone receptors and the coactivator TIF2Identification of an autonomous transactivation domain in helix H3 of the vitamin D receptor.Nuclear receptors: the evolution of diversity.Transcriptional silencing is defined by isoform- and heterodimer-specific interactions between nuclear hormone receptors and corepressorsThe CoRNR motif controls the recruitment of corepressors by nuclear hormone receptors.Segmentation gene product Fushi tarazu is an LXXLL motif-dependent coactivator for orphan receptor FTZ-F1Functional diversification of vitamin D receptor paralogs in teleost fish after a whole genome duplication eventLigand binding was acquired during evolution of nuclear receptorsThe RXRalpha C-terminus T462 is a NMR sensor for coactivator peptide bindingRetinoid X receptor (RXR) within the RXR-retinoic acid receptor heterodimer binds its ligand and enhances retinoid-dependent gene expression.A conformational switch in nuclear hormone receptors is involved in coupling hormone binding to corepressor releaseCorepressor SMRT binds the BTB/POZ repressing domain of the LAZ3/BCL6 oncoproteinTranscriptional anti-repression. Thyroid hormone receptor beta-2 recruits SMRT corepressor but interferes with subsequent assembly of a functional corepressor complex.Vitamin D-dependent recruitment of corepressors to vitamin D/retinoid X receptor heterodimersFlow signaling and atherosclerosis.A novel role for helix 12 of retinoid X receptor in regulating repression.tau4/tau c/AF-2 of the thyroid hormone receptor relieves silencing of the retinoic acid receptor silencer core independent of both tau4 activation function and full dissociation of corepressors.Determinants of CoRNR-dependent repression complex assembly on nuclear hormone receptors.Ligand-dependent degradation of retinoid X receptors does not require transcriptional activity or coactivator interactions.Transactivation by retinoid X receptor-peroxisome proliferator-activated receptor gamma (PPARgamma) heterodimers: intermolecular synergy requires only the PPARgamma hormone-dependent activation functionDifferential recognition of liganded and unliganded thyroid hormone receptor by retinoid X receptor regulates transcriptional repression.Aberrant association of promyelocytic leukemia protein-retinoic acid receptor-alpha with coactivators contributes to its ability to regulate gene expression.Co-repressor release but not ligand binding is a prerequisite for transcription activation by human retinoid acid receptor alpha ligand-binding domain.Transcriptional repression by thyroid hormone receptors. A role for receptor homodimers in the recruitment of SMRT corepressor.Signaling by tyrosine kinases negatively regulates the interaction between transcription factors and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) corepressor.Mutations in the 1,25-dihydroxyvitamin D3 receptor identifying C-terminal amino acids required for transcriptional activation that are functionally dissociated from hormone binding, heterodimeric DNA binding, and interaction with basal transcriptionGenetic variability and evolution of two pharmacologically important classes of genes.Identification of a cDNA encoding a retinoid X receptor homologue from Schistosoma mansoni. Evidence for a role in female-specific gene expression.Ligand-Dependent Corepressor (LCoR) Is A Rexinoid-Inhibited PPARγ-RXRα Coactivator.Activity of the Nurr1 Carboxyl-terminal Domain Depends on Cell Type and Integrity of the Activation Function 2
P2860
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P2860
Activation and repression by nuclear hormone receptors: hormone modulates an equilibrium between active and repressive states.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Activation and repression by n ...... active and repressive states.
@ast
Activation and repression by n ...... active and repressive states.
@en
type
label
Activation and repression by n ...... active and repressive states.
@ast
Activation and repression by n ...... active and repressive states.
@en
prefLabel
Activation and repression by n ...... active and repressive states.
@ast
Activation and repression by n ...... active and repressive states.
@en
P2093
P2860
P356
P1476
Activation and repression by n ...... active and repressive states.
@en
P2093
H Juguilon
I G Schulman
P2860
P304
P356
10.1128/MCB.16.7.3807
P407
P577
1996-07-01T00:00:00Z