about
Crosstalk of HNF4α with extracellular and intracellular signaling pathways in the regulation of hepatic metabolism of drugs and lipidsGATA4 Is Sufficient to Establish Jejunal Versus Ileal Identity in the Small Intestine.Non-cell-autonomous activation of IL-6/STAT3 signaling mediates FGF19-driven hepatocarcinogenesis.An Intestinal Microbiota-Farnesoid X Receptor Axis Modulates Metabolic Disease.Short bowel syndrome results in increased gene expression associated with proliferation, inflammation, bile acid synthesis and immune system activation: RNA sequencing a zebrafish SBS modelPostnatal Deletion of Fat Storage-inducing Transmembrane Protein 2 (FIT2/FITM2) Causes Lethal Enteropathy.Liver ChIP-seq analysis in FGF19-treated mice reveals SHP as a global transcriptional partner of SREBP-2.FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho.Targeting Bile Acid Receptors: Discovery of a Potent and Selective Farnesoid X Receptor Agonist as a New Lead in the Pharmacological Approach to Liver Diseases.Role of farnesoid X receptor in cholestasis.Bile acids and cardiovascular function in cirrhosis.Nutrient-sensing nuclear receptors PPARα and FXR control liver energy balance.A Randomized Trial of Obeticholic Acid Monotherapy in Patients with Primary Biliary Cholangitis.RNA-binding protein ZFP36L1 maintains posttranscriptional regulation of bile acid metabolism.Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System.Nonalcoholic Fatty Liver Disease as a Nexus of Metabolic and Hepatic Diseases.A gut-brain axis regulating glucose metabolism mediated by bile acids and competitive fibroblast growth factor actions at the hypothalamus.Complex interaction between circadian rhythm and diet on bile acid homeostasis in male rats.Targeting the brain as a cure for type 2 diabetes.Development and Characterization of a Human and Mouse Intestinal Epithelial Cell Monolayer Platform.AhR and SHP regulate phosphatidylcholine and S-adenosylmethionine levels in the one-carbon cycle.Effects of supplemented isoenergetic diets varying in cereal fiber and protein content on the bile acid metabolic signature and relation to insulin resistance.Gut Microbes and Health: A Focus on the Mechanisms Linking Microbes, Obesity, and Related Disorders.Engineered FGF19 eliminates bile acid toxicity and lipotoxicity leading to resolution of steatohepatitis and fibrosis in mice.MAFB mediates the therapeutic effect of sleeve gastrectomy for obese diabetes mellitus by activation of FXR expression.Postprandial FGF19-induced phosphorylation by Src is critical for FXR function in bile acid homeostasis.NGM282 for Treatment of Patients With Primary Biliary Cholangitis: A Multicenter, Randomized, Double-Blind, Placebo-Controlled TrialThe exercise-inducible bile acid receptor Tgr5 improves skeletal muscle function in miceEssential roles of bile acids and their nuclear receptors, FXR and PXR, in the cholestatic liver disease
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@ast
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@en
type
label
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@ast
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@en
prefLabel
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@ast
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@en
P2860
P356
P1433
P1476
Bile Acids as Hormones: The FXR-FGF15/19 Pathway
@en
P2093
Steven A Kliewer
P2860
P304
P356
10.1159/000371670
P577
2015-05-27T00:00:00Z