Identification of a chemical tool for the orphan nuclear receptor FXR.
about
Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesisIdentification of farnesoid X receptor beta as a novel mammalian nuclear receptor sensing lanosterolInvolvement of corepressor complex subunit GPS2 in transcriptional pathways governing human bile acid biosynthesisPeroxisome proliferator-activated receptor-gamma coactivator 1alpha (PGC-1alpha) regulates triglyceride metabolism by activation of the nuclear receptor FXRFXR signaling in the enterohepatic systemIdentification of a potent synthetic FXR agonist with an unexpected mode of binding and activationBile acid nuclear receptor FXR and digestive system diseasesRole of farnesoid X receptor and bile acids in alcoholic liver diseaseDiacylglycerol kinase θ couples farnesoid X receptor-dependent bile acid signalling to Akt activation and glucose homoeostasis in hepatocytesSyndecan-1 expression is regulated in an isoform-specific manner by the farnesoid-X receptorThe farnesoid X receptor controls gene expression in a ligand- and promoter-selective fashionThe human apolipoprotein AV gene is regulated by peroxisome proliferator-activated receptor-alpha and contains a novel farnesoid X-activated receptor response elementFarnesoid X receptor regulates bile acid-amino acid conjugationMAFG is a transcriptional repressor of bile acid synthesis and metabolismFarnesoid X receptor agonists attenuate colonic epithelial secretory function and prevent experimental diarrhoea in vivoRegulation of antibacterial defense in the small intestine by the nuclear bile acid receptorFXR-mediated regulation of eNOS expression in vascular endothelial cellsThe farnesoid X receptor modulates adiposity and peripheral insulin sensitivity in miceFarnesoid X Receptor an Emerging Target to Combat Obesity.Structural overview of the nuclear receptor superfamily: insights into physiology and therapeutics.The Concise Guide to PHARMACOLOGY 2013/14: nuclear hormone receptors.LXR ligand lowers LDL cholesterol in primates, is lipid neutral in hamster, and reduces atherosclerosis in mouseExposure to the synthetic FXR agonist GW4064 causes alterations in gene expression and sublethal hepatotoxicity in eleutheroembryo medaka (Oryzias latipes)NSAIDs Ibuprofen, Indometacin, and Diclofenac do not interact with Farnesoid X Receptor.Bile acid receptor agonist GW4064 regulates PPARγ coactivator-1α expression through estrogen receptor-related receptor αFarnesoid X receptor protects liver cells from apoptosis induced by serum deprivation in vitro and fasting in vivo.Identification of novel pathways that control farnesoid X receptor-mediated hypocholesterolemia.Clinical application of transcriptional activators of bile salt transporters.Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1cTwo farnesoid X receptor alpha isoforms in Japanese medaka (Oryzias latipes) are differentially activated in vitro.The hypolipidemic agent guggulsterone regulates the expression of human bile salt export pump: dominance of transactivation over farsenoid X receptor-mediated antagonismBile acids regulate hepatic gluconeogenic genes and farnesoid X receptor via G(alpha)i-protein-coupled receptors and the AKT pathway.Farnesoid X receptor activation mediates head-to-tail chromatin looping in the Nr0b2 gene encoding small heterodimer partner.Identification of trisubstituted-pyrazol carboxamide analogs as novel and potent antagonists of farnesoid X receptor.Activation of the farnesoid X receptor provides protection against acetaminophen-induced hepatic toxicity.Activation of the nuclear receptor FXR improves hyperglycemia and hyperlipidemia in diabetic mice.Orphan nuclear receptors as eLiXiRs and FiXeRs of sterol metabolism.Synthetic FXR agonist GW4064 prevents diet-induced hepatic steatosis and insulin resistance.Chemical genomics: functional analysis of orphan nuclear receptors in the regulation of bile acid metabolism.Tissue specific induction of p62/Sqstm1 by farnesoid X receptor.
P2860
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P2860
Identification of a chemical tool for the orphan nuclear receptor FXR.
description
2000 nî lūn-bûn
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2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Identification of a chemical tool for the orphan nuclear receptor FXR.
@ast
Identification of a chemical tool for the orphan nuclear receptor FXR.
@en
type
label
Identification of a chemical tool for the orphan nuclear receptor FXR.
@ast
Identification of a chemical tool for the orphan nuclear receptor FXR.
@en
prefLabel
Identification of a chemical tool for the orphan nuclear receptor FXR.
@ast
Identification of a chemical tool for the orphan nuclear receptor FXR.
@en
P2093
P356
P1476
Identification of a chemical tool for the orphan nuclear receptor FXR.
@en
P2093
Haffner CD
Maloney PR
Plunket KD
P304
P356
10.1021/JM0002127
P407
P577
2000-08-01T00:00:00Z