RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding - Wikidata - wikimedia - TriplyDB

RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding

RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding

http://www.wikidata.org/entity/Q28217579

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Regulation of IkappaBalpha function and NF-kappaB signaling: AEBP1 is a novel proinflammatory mediator in macrophages Altered subcellular distribution of MSK1 induced by glucocorticoids contributes to NF-kappaB inhibition.Corepressors: custom tailoring and alterations while you wait.The three-dimensional structures of antagonistic and agonistic forms of the glucocorticoid receptor ligand-binding domain: RU-486 induces a transconformation that leads to active antagonism Differential cytokine profiles upon comparing selective versus classic glucocorticoid receptor modulation in human peripheral blood mononuclear cells and inferior turbinate tissue Regulation of the rat UGT1A6 by glucocorticoids involves a cryptic glucocorticoid response element Dual role for glucocorticoids in cardiomyocyte hypertrophy and apoptosis All-trans retinoic acid-induced hypothalamus-pituitary-adrenal hyperactivity involves glucocorticoid receptor dysregulation.RU486 did not exacerbate cytokine release in mice challenged with LPS nor in db/db mice.A Quantitative Study of Internal and External Interactions of Homodimeric Glucocorticoid Receptor Using Fluorescence Cross-Correlation Spectroscopy in a Live Cell.Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids.Dexamethasone and corticosterone induce similar, but not identical, muscle wasting responses in cultured L6 and C2C12 myotubes Ethanol upregulates glucocorticoid-induced leucine zipper expression and modulates cellular inflammatory responses in lung epithelial cells The androgen receptor recruits nuclear receptor CoRepressor (N-CoR) in the presence of mifepristone via its N and C termini revealing a novel molecular mechanism for androgen receptor antagonists.Conformational changes of the glucocorticoid receptor ligand binding domain induced by ligand and cofactor binding, and the location of cofactor binding sites determined by hydrogen/deuterium exchange mass spectrometry Current and potential rodent screens and tests for thyroid toxicants.Differential targeting of brain stress circuits with a selective glucocorticoid receptor modulator.High activity of the stress promoter contributes to susceptibility to stress in the tree shrew Low concentrations of corticosterone exert stimulatory effects on macrophage function in a manner dependent on glucocorticoid receptors.Human glucocorticoid receptor isoform beta: recent understanding of its potential implications in physiology and pathophysiology.A novel principle for partial agonism of liver X receptor ligands. Competitive recruitment of activators and repressors.The Smad6-histone deacetylase 3 complex silences the transcriptional activity of the glucocorticoid receptor: potential clinical implications.Nuclear compartmentalization of N-CoR and its interactions with steroid receptors.Agonist-specific Protein Interactomes of Glucocorticoid and Androgen Receptor as Revealed by Proximity Mapping.The Interactome of the Glucocorticoid Receptor and Its Influence on the Actions of Glucocorticoids in Combatting Inflammatory and Infectious Diseases.Understanding how long-acting β2 -adrenoceptor agonists enhance the clinical efficacy of inhaled corticosteroids in asthma - an update.Antiandrogenic activity of anthranilic acid ester derivatives as novel lead structures to inhibit prostate cancer cell proliferation.Regulation of glucocorticoid receptor activity by a stress responsive transcriptional cofactor.The natural compound atraric acid is an antagonist of the human androgen receptor inhibiting cellular invasiveness and prostate cancer cell growth.Dual regulation of glucocorticoid-induced leucine zipper (GILZ) by the glucocorticoid receptor and the PI3-kinase/AKT pathways in multiple myeloma.Structural basis for nuclear receptor corepressor recruitment by antagonist-liganded androgen receptor.Protein kinase A phosphorylates NCoR to enhance its nuclear translocation and repressive function in human prostate cancer cells.Dexamethasone suppresses JMJD3 gene activation via a putative negative glucocorticoid response element and maintains integrity of tight junctions in brain microvascular endothelial cells.Probing Dominant Negative Behavior of Glucocorticoid Receptor β through a Hybrid Structural and Biochemical Approach.

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RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding

http://www.wikidata.org/entity/Q28217579

description

2002 nî lūn-bûn

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2002 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2002年の論文

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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Journal of Biological Chemistry

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RU486-induced glucocorticoid r ...... nus and by corepressor binding

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P2093

Anja Dostert

http://www.w3.org/2001/XMLSchema#string

Aria Baniahmad

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Martin Eggert

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Martin Schulz

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Rainer Renkawitz

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Thorsten Heinzel

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P2860

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

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

Sharp, an inducible cofactor that integrates nuclear receptor repression and activation

GRIP1, a transcriptional coactivator for the AF-2 transactivation domain of steroid, thyroid, retinoid, and vitamin D receptors

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

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

High-efficiency transformation of mammalian cells by plasmid DNA

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

The nuclear receptor superfamily: the second decade

What's up and down with histone deacetylation and transcription?

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26238-43

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scholarly article

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1993473

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10.1074/JBC.M203268200

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29

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277

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12011091

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