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hepatocytes

Carbon Tetrachloride Induced Mitochondrial Division, Respiratory Chain Damage, Abnormal Intracellular [H+] and Apoptosis Are Due to the Activation of 5-HT Degradation System in Hepatocytes

[Toxicology and Applied Pharmacology] The authors determined the role of the 5-HT degradation system in mitochondrial damage and apoptosis of hepatocytes.

Bile Acid and Receptors: Biology and Drug Discovery for Nonalcoholic Fatty Liver Disease

[Acta Pharmacologica Sinica] Scientists summarize the current knowledge on the role of bile acids and the receptors in the development of nonalcoholic fatty liver disease and nnonalcoholic steatohepatitis, especially the functions of farnesoid X receptor in different tissues including liver and intestine.

Differential Expression of HNF1A and HNF1A-AS1 in Colon Cancer Cells

[IUBMB Life] Scientists determined the epigenetic features of the HNF1A gene loci, and expression and cellular localization of HNF1A-AS1 RNA, HNF1A RNA, and HNF1A protein in colorectal cancer and normal colon epithelial cells.

Long Noncoding RNA SNHG1 Silencing Accelerates Hepatocyte-Like Cell Differentiation of Bone Marrow-Derived Mesenchymal Stem Cells to Alleviate Cirrhosis via the microRNA-15a/SMURF1/UVRAG Axis

[Cell Death Discovery] Researchers investigated whether long noncoding RNA SNHG1 was involved in cirrhosis by affecting hepatocyte-like cell differentiation of bone marrow-derived MSCs.

Resveratrol Induces the Fasting State and Alters Circadian Metabolism in Hepatocytes

[Plant Foods For Human Nutrition] Investigators studied the metabolic effect of resveratrol around the circadian clock in order to determine more accurately the hepatic signaling pathways involved. AML-12 hepatocytes were treated with resveratrol and clock and metabolic markers were measured around the clock.

Cell Adhesion Molecule KIRREL1 Is a Feedback Regulator of Hippo Signaling Recruiting SAV1 to Cell-Cell Contact Sites

[Nature Communications] The authors suggested that KIRREL1 functioned as a feedback regulator of the mammalian Hippo pathway through sensing cell-cell interaction and recruiting SAV1 to cell-cell contact sites.

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