Bile acid-induced Mallory body formation in drug-primed mouse liver. - Wikidata - awgldk - TriplyDB

Bile acid-induced Mallory body formation in drug-primed mouse liver.

Bile acid-induced Mallory body formation in drug-primed mouse liver.

http://www.wikidata.org/entity/Q35748180

about

Autophagy and apoptosis in liver injury Role of p62/SQSTM1 in liver physiology and pathogenesis A new xenobiotic-induced mouse model of sclerosing cholangitis and biliary fibrosis Hepatotoxin-induced changes in the adult murine liver promote MYC-induced tumorigenesis Epigenetic mechanisms regulate Mallory Denk body formation in the livers of drug-primed mice Intermediate filaments control the intracellular distribution of caspases during apoptosis.The keratin cytoskeleton in liver diseases.Comparison of murine cirrhosis models induced by hepatotoxin administration and common bile duct ligation.Expression and localization of sterile alpha motif domain containing 5 is associated with cell type and malignancy of biliary tree Intermediate filament cytoskeleton of the liver in health and disease Bile acids promote diethylnitrosamine-induced hepatocellular carcinoma via increased inflammatory signaling.Farnesoid X receptor critically determines the fibrotic response in mice but is expressed to a low extent in human hepatic stellate cells and periductal myofibroblasts.Xenobiotic-induced liver injury and fibrosis.Animal models of biliary injury and altered bile acid metabolism.The establishment and characterization of immortal hepatocyte cell lines from a mouse liver injury model.Cardiomyopathy reverses with recovery of liver injury, cholestasis and cholanemia in mouse model of biliary fibrosis Hypertrophic cardiomyopathy and dysregulation of cardiac energetics in a mouse model of biliary fibrosis Impaired bile acid handling and aggravated liver injury in mice expressing a hepatocyte-specific RXRα variant lacking the DNA-binding domain.Gene expression profiling in rat liver treated with compounds inducing elevation of bilirubin.Role of nuclear receptors and hepatocyte-enriched transcription factors for Ntcp repression in biliary obstruction in mouse liver.Degradation of the sodium taurocholate cotransporting polypeptide (NTCP) by the ubiquitin-proteasome system.Characterization of time-related changes after experimental bile duct ligation.Dysregulated Bile Transporters and Impaired Tight Junctions During Chronic Liver Injury in Mice

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P2860

Bile acid-induced Mallory body formation in drug-primed mouse liver.

http://www.wikidata.org/entity/Q35748180

description

2002 nî lūn-bûn

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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2002年论文

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2002年论文

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name

Bile acid-induced Mallory body formation in drug-primed mouse liver.

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Bile acid-induced Mallory body formation in drug-primed mouse liver.

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type

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Bile acid-induced Mallory body formation in drug-primed mouse liver.

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Bile acid-induced Mallory body formation in drug-primed mouse liver.

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Bile acid-induced Mallory body formation in drug-primed mouse liver.

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Bile acid-induced Mallory body formation in drug-primed mouse liver.

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S0002-9440(10)64480-X

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The American Journal of Pathology

P1476

Bile acid-induced Mallory body formation in drug-primed mouse liver.

@en

P2093

Andrea Fuchsbichler

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Conny Stumptner

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Helmut Denk

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Michael Trauner

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Peter Fickert

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P2860

Mutation of human keratin 18 in association with cryptogenic cirrhosis

The continuing importance of bile acids in liver and intestinal disease

Stress, apoptosis, and mitosis induce phosphorylation of human keratin 8 at Ser-73 in tissues and cultured cells

Conformational disease

The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells

Cytokeratin 8 protects from hepatotoxicity, and its ratio to cytokeratin 18 determines the ability of hepatocytes to form Mallory bodies

NF-kappaB is activated in cholestasis and functions to reduce liver injury

Susceptibility to hepatotoxicity in transgenic mice that express a dominant-negative human keratin 18 mutant

Keratin-dependent, epithelial resistance to tumor necrosis factor-induced apoptosis

The ubiquitin system for protein degradation

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2019-2026

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10.1016/S0002-9440(10)64480-X

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