Regulation of adipogenesis by natural and synthetic REV-ERB ligands. - Wikidata - awgldk - TriplyDB

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

http://www.wikidata.org/entity/Q33993896

about

DBC1 (Deleted in Breast Cancer 1) modulates the stability and function of the nuclear receptor Rev-erbα Regulation of circadian behaviour and metabolism by synthetic REV-ERB agonists Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer Orphan nuclear receptors and the regulation of nutrient metabolism: understanding obesity Road to exercise mimetics: targeting nuclear receptors in skeletal muscle Circadian regulation of adipose function Structure of REV-ERB Ligand-binding Domain Bound to a Porphyrin Antagonist Direct regulation of CLOCK expression by REV-ERB.Endocrine disrupting chemicals and the developmental programming of adipogenesis and obesity Therapeutic Effect of a Synthetic RORα/γ Agonist in an Animal Model of Autism Examination of nuclear receptor expression in osteoblasts reveals Rorβ as an important regulator of osteogenesis Novel role of nuclear receptor Rev-erbα in hepatic stellate cell activation: potential therapeutic target for liver injury Characteristics of the heme catabolic pathway in mild unconjugated hyperbilirubinemia and their associations with inflammation and disease prevention REV-ERB-ALPHA circadian gene variant associates with obesity in two independent populations: Mediterranean and North American.Rev-Erb co-regulates muscle regeneration via tethered interaction with the NF-Y cistrome Translational Significance of Heme Oxygenase in Obesity and Metabolic Syndrome Increased adipose tissue heme levels and exportation are associated with altered systemic glucose metabolism.HO-1 Upregulation Attenuates Adipocyte Dysfunction, Obesity, and Isoprostane Levels in Mice Fed High Fructose Diets.Regulation of circadian behaviour and metabolism by REV-ERB-α and REV-ERB-β.Rev-erbα and Rev-erbβ coordinately protect the circadian clock and normal metabolic function REV-ERB and ROR nuclear receptors as drug targets.Identification of SR1078, a synthetic agonist for the orphan nuclear receptors RORα and RORγ.Identification of SR8278, a synthetic antagonist of the nuclear heme receptor REV-ERB.Identification of SR3335 (ML-176): a synthetic RORα selective inverse agonist Administration of heme arginate ameliorates murine type 2 diabetes independently of heme oxygenase activity.The REV-ERBs and RORs: molecular links between circadian rhythms and lipid homeostasis.Current methods of adipogenic differentiation of mesenchymal stem cells Alternative mRNA splicing of corepressors generates variants that play opposing roles in adipocyte differentiation.The nuclear receptor REV-ERBα mediates circadian regulation of innate immunity through selective regulation of inflammatory cytokines.Novel Function of Rev-erbα in Promoting Brown Adipogenesis Anti-proliferative actions of a synthetic REV-ERBα/β agonist in breast cancer cells.Impact of 3-Amino-1,2,4-Triazole (3-AT)-Derived Increase in Hydrogen Peroxide Levels on Inflammation and Metabolism in Human Differentiated Adipocytes High Affinity Heme Binding to a Heme Regulatory Motif on the Nuclear Receptor Rev-erbβ Leads to Its Degradation and Indirectly Regulates Its Interaction with Nuclear Receptor Corepressor Dual inhibition of REV-ERBβ and autophagy as a novel pharmacological approach to induce cytotoxicity in cancer cells Biological aging alters circadian mechanisms in murine adipose tissue depots Epoxyeicosatrienoic Acids Regulate Adipocyte Differentiation of Mouse 3T3 Cells, Via PGC-1α Activation, Which Is Required for HO-1 Expression and Increased Mitochondrial Function Increased atherosclerotic lesions in LDL receptor deficient mice with hematopoietic nuclear receptor Rev-erbα knock- down.Increased HO-1 levels ameliorate fatty liver development through a reduction of heme and recruitment of FGF21.How to fix a broken clock.REV-ERBα influences the stability and nuclear localization of the glucocorticoid receptor.

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Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

http://www.wikidata.org/entity/Q33993896

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

@ast

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

@en

type

label

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

@ast

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

@en

prefLabel

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

@ast

Regulation of adipogenesis by natural and synthetic REV-ERB ligands.

@en

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Regulation of adipogenesis by natural and synthetic REV-ERB ligands

@en

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Christine Crumbley

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

Gargi Bhattacharyya

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

Jeffrey M Gimble

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Keith R Stayrook

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

Laura A Solt

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

Naresh Kumar

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Pamela M Rogers

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Patrick R Griffin

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

Theodore M Kamenecka

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

Yongjun Wang

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P2860

Rev-erbalpha, a heme sensor that coordinates metabolic and circadian pathways

Identification of heme as the ligand for the orphan nuclear receptors REV-ERBalpha and REV-ERBbeta.

Ligand modulation of REV-ERBalpha function resets the peripheral circadian clock in a phasic manner

Bifunctional role of Rev-erbalpha in adipocyte differentiation

Adipocyte differentiation from the inside out

PGC-1alpha negatively regulates hepatic FGF21 expression by modulating the heme/Rev-Erb(alpha) axis.

The nuclear hormone receptor family round the clock.

Nuclear hormone receptors for heme: REV-ERBalpha and REV-ERBbeta are ligand-regulated components of the mammalian clock.

The 26S proteasome is required for estrogen receptor-alpha and coactivator turnover and for efficient estrogen receptor-alpha transactivation.

NPAS2: a gas-responsive transcription factor.

P304

3015-3025

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scholarly article

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10.1210/EN.2009-0800

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7

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151

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Z. Elizabeth Floyd

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2010-04-28T00:00:00Z

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43351535

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20427485

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2903944

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