Dose-response of five bile acids on serum and liver bile Acid concentrations and hepatotoxicty in mice.
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Functional Intestinal Bile Acid 7α-Dehydroxylation by Clostridium scindens Associated with Protection from Clostridium difficile Infection in a Gnotobiotic Mouse ModelLithocholic acid feeding results in direct hepato-toxicity independent of neutrophil function in miceGender-divergent profile of bile acid homeostasis during aging of mice.Bile acid dysregulation, gut dysbiosis, and gastrointestinal cancer.Assessment of benzene-induced hematotoxicity using a human-like hematopoietic lineage in NOD/Shi-scid/IL-2Rγnull micePotency of individual bile acids to regulate bile acid synthesis and transport genes in primary human hepatocyte cultures.Bile acids regulate nuclear receptor (Nur77) expression and intracellular location to control proliferation and apoptosis.Imaging of whole zebra fish (Danio rerio) by desorption electrospray ionization mass spectrometry.Cholic acid induces a Cftr dependent biliary secretion and liver growth response in mice.TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice.Bile Acids and Dysbiosis in Non-Alcoholic Fatty Liver Disease.Importance of Large Intestine in Regulating Bile Acids and Glucagon-Like Peptide-1 in Germ-Free Mice.Dose-response effect of berberine on bile acid profile and gut microbiota in mice.Preference of Conjugated Bile Acids over Unconjugated Bile Acids as Substrates for OATP1B1 and OATP1B3.Hepatotoxicity due to chenodeoxycholic acid supplementation in an infant with cerebrotendinous xanthomatosis: implications for treatment.Metabolomics reveals an essential role for peroxisome proliferator-activated receptor α in bile acid homeostasis.Decreased hepatotoxic bile acid composition and altered synthesis in progressive human nonalcoholic fatty liver disease.Activation of Constitutive Androstane Receptor (CAR) in Mice Results in Maintained Biliary Excretion of Bile Acids Despite a Marked Decrease of Bile Acids in LiverRole of glucuronidation for hepatic detoxification and urinary elimination of toxic bile acids during biliary obstruction.Sex-dependent effects on gut microbiota regulate hepatic carcinogenic outcomes.Linking physiology to toxicity using DILIsym®, a mechanistic mathematical model of drug-induced liver injury.Modulation of the gut microbiota impacts nonalcoholic fatty liver disease: a potential role for bile acids.L-arginine conjugates of bile acids-a possible treatment for non-alcoholic fatty liver disease.Hepatitis B virus surface proteins accelerate cholestatic injury and tumor progression in Abcb4-knockout mice.Effect of various antibiotics on modulation of intestinal microbiota and bile acid profile in miceBile acid: a potential inducer of colon cancer stem cells.Atypical clinical presentation and successful treatment with oral cholic acid of a child with defective bile acid synthesis due to a novel mutation in the HSD3B7 geneUrinary bile acids as biomarkers for liver diseases II. Signature profiles in patients.IL-17A synergistically enhances bile acid-induced inflammation during obstructive cholestasis.The receptor TGR5 protects the liver from bile acid overload during liver regeneration in mice.Modulation of the intestinal bile acid-FXR-FGF15 axis improves alcoholic liver disease in mice.Bile acids induce activation of alveolar epithelial cells and lung fibroblasts through farnesoid X receptor-dependent and independent pathways.A gut-brain axis regulating glucose metabolism mediated by bile acids and competitive fibroblast growth factor actions at the hypothalamus.Reduction in hepatic secondary bile acids caused by short-term antibiotic-induced dysbiosis decreases mouse serum glucose and triglyceride levels.A fermented sorghum/millet-based beverage, Obiolor, extenuates high-fat diet-induced dyslipidaemia and redox imbalance in the livers of rats.Bile acid-induced expression of farnesoid X receptor as the basis for superiority of internal biliary drainage in experimental biliary obstructionHigh Dose and Delayed Treatment with Bile Acids Ineffective in RML Prion-Infected Mice
P2860
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P2860
Dose-response of five bile acids on serum and liver bile Acid concentrations and hepatotoxicty in mice.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@ast
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@en
type
label
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@ast
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@en
prefLabel
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@ast
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@en
P2093
P2860
P356
P1476
Dose-response of five bile aci ...... ons and hepatotoxicty in mice.
@en
P2093
Curtis D Klaassen
Peizhen Song
Youcai Zhang
P2860
P304
P356
10.1093/TOXSCI/KFR177
P577
2011-07-11T00:00:00Z