Human hepatoblastoma cells (HepG2) and rat hepatoma cells are defective in important enzyme activities in the oxidation of the C27 steroid side chain in bile acid formation
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference48 articles.
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1. Predominance of human versus rat phenotype in the metabolic pathways for bile acid synthesis by hybrid WIF-B9 cells;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2001-11
2. Primary cultures of human hepatocytes but not HepG2 hepatoblastoma cells are suitable for the study of glycosidic conjugation of bile acids;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2001-02
3. Selective uptake of cholesteryl ester from low density lipoprotein is involved in HepG2 cell cholesterol homeostasis;European Journal of Biochemistry;1999-07-15
4. Maturation of peroxisomes in differentiating human hepatoblastoma cells (HepG2): possible involvement of the peroxisome proliferator-activated receptor α (PPARα);Differentiation;1998-11
5. Differences in hypolipidaemic effects of two statins on Hep G2 cells or human hepatocytes in primary culture;British Journal of Pharmacology;1996-08
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