Bile acids regulate gluconeogenic gene expression via small heterodimer partner-mediated repression of hepatocyte nuclear factor 4 and Foxo1.
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Hypoxia induces PDK4 gene expression through induction of the orphan nuclear receptor ERRγDAX-1 acts as a novel corepressor of orphan nuclear receptor HNF4alpha and negatively regulates gluconeogenic enzyme gene expressionTranscriptional corepressor SMILE recruits SIRT1 to inhibit nuclear receptor estrogen receptor-related receptor gamma transactivationThe role of bile after Roux-en-Y gastric bypass in promoting weight loss and improving glycaemic controlRole of bile acids in the regulation of the metabolic pathwaysInflammation Meets Metabolic Disease: Gut Feeling Mediated by GLP-1Bile acid receptors and nonalcoholic fatty liver diseaseOrphan nuclear receptors and the regulation of nutrient metabolism: understanding obesityIntestinal microbiota and type 2 diabetes: from mechanism insights to therapeutic perspectiveBile acid metabolism and signalingModulation of the transcriptional activity of peroxisome proliferator-activated receptor gamma by protein-protein interactions and post-translational modificationsBile acids, obesity, and the metabolic syndromeBile acid sequestration reduces plasma glucose levels in db/db mice by increasing its metabolic clearance rateBile Acids Promote the Expression of Hepatitis C Virus in Replicon-Harboring CellsThe interplay of the gut microbiome, bile acids, and volatile organic compoundsBile acid nuclear receptor FXR and digestive system diseasesThe nuclear receptor FXR is expressed in pancreatic beta-cells and protects human islets from lipotoxicityBile acid signaling in metabolic disease and drug therapyThe farnesoid X receptor modulates adiposity and peripheral insulin sensitivity in miceFarnesoid X receptor is essential for normal glucose homeostasisRole of nuclear receptor SHP in metabolism and cancer.Bile acids and metabolic regulation: mechanisms and clinical responses to bile acid sequestration.Orphan nuclear receptor small heterodimer partner inhibits angiotensin II- stimulated PAI-1 expression in vascular smooth muscle cells.Colesevelam lowers glucose and lipid levels in type 2 diabetes: the clinical evidence.Nuclear receptors: mediators and modifiers of inflammation-induced cholestasis.Bile acids regulate hepatic gluconeogenic genes and farnesoid X receptor via G(alpha)i-protein-coupled receptors and the AKT pathway.Bile acid metabolites in serum: intraindividual variation and associations with coronary heart disease, metabolic syndrome and diabetes mellitusAMPK-dependent repression of hepatic gluconeogenesis via disruption of CREB.CRTC2 complex by orphan nuclear receptor small heterodimer partner.Activation of the nuclear receptor FXR improves hyperglycemia and hyperlipidemia in diabetic mice.A comparative study of genome-wide transcriptional profiles of primary hepatocytes in collagen sandwich and monolayer cultures.Endocrine functions of bile acids.Sodium arsenite induces orphan nuclear receptor SHP gene expression via AMP-activated protein kinase to inhibit gluconeogenic enzyme gene expression.Feedback regulation of hepatic gluconeogenesis through modulation of SHP/Nr0b2 gene expression by Sirt1 and FoxO1.Deciphering the nuclear bile acid receptor FXR paradigm.Nonalcoholic fatty liver disease: molecular pathways and therapeutic strategiesRNAi screening in primary human hepatocytes of genes implicated in genome-wide association studies for roles in type 2 diabetes identifies roles for CAMK1D and CDKAL1, among others, in hepatic glucose regulation.Insulin regulation of cholesterol 7alpha-hydroxylase expression in human hepatocytes: roles of forkhead box O1 and sterol regulatory element-binding protein 1c.Bile Acid signaling in liver metabolism and diseases.Inhibitory effects of bile acids and synthetic farnesoid X receptor agonists on rotavirus replication.Characterization of novel peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) isoform in human liver.
P2860
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P2860
Bile acids regulate gluconeogenic gene expression via small heterodimer partner-mediated repression of hepatocyte nuclear factor 4 and Foxo1.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Bile acids regulate gluconeoge ...... te nuclear factor 4 and Foxo1.
@en
type
label
Bile acids regulate gluconeoge ...... te nuclear factor 4 and Foxo1.
@en
prefLabel
Bile acids regulate gluconeoge ...... te nuclear factor 4 and Foxo1.
@en
P2093
P2860
P356
P1476
Bile acids regulate gluconeoge ...... yte nuclear factor 4 and Foxo1
@en
P2093
Akiyoshi Fukamizu
Hiroaki Daitoku
Hitomi Matsuzaki
Junji Ishida
Keiko Hirota
Yoko Shimamoto
P2860
P304
23158-23165
P356
10.1074/JBC.M314322200
P407
P577
2004-03-26T00:00:00Z