Effect of 3- and 4-thia-substituted fatty acids on glycerolipid metabolism and mitochondrial beta-oxidation in rat liver.

[1]  A. Svardal,et al.  Fatty acid metabolism in liver of rats treated with hypolipidemic sulphur-substituted fatty acid analogues. , 1990, Biochimica et biophysica acta.

[2]  R. Berge,et al.  Alkylthio acetic acids (3-thia fatty acids)--a new group of non-beta-oxidizable peroxisome-inducing fatty acid analogues--II. Dose-response studies on hepatic peroxisomal- and mitochondrial changes and long-chain fatty acid metabolizing enzymes in rats. , 1989, Biochemical pharmacology.

[3]  R. Berge,et al.  Alkylthioacetic acids (3-thia fatty acids) as non-beta-oxidizable fatty acid analogues: a new group of hypolipidemic drugs. III. Dissociation of cholesterol- and triglyceride-lowering effects and the induction of peroxisomal beta-oxidation. , 1989, Journal of lipid research.

[4]  R. Berge,et al.  Alkylthioacetic acid (3-thia fatty acids)--a new group of non-beta-oxidizable, peroxisome-inducing fatty acid analogues. I. A study on the structural requirements for proliferation of peroxisomes and mitochondria in rat liver. , 1989, Biochimica et biophysica acta.

[5]  J. Bremer,et al.  Induction of peroxisomal beta-oxidation in 7800 C1 Morris hepatoma cells in steady state by fatty acids and fatty acid analogues. , 1989, Biochimica et biophysica acta.

[6]  A. Poulos,et al.  Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts. , 1989, Archives of biochemistry and biophysics.

[7]  D. Hardeman,et al.  Rat liver dihydroxyacetone-phosphate acyltransferase: enzyme characteristics and localization studies. , 1988, Biochimica et biophysica acta.

[8]  C. Drevon,et al.  Eicosapentaenoic acid inhibits cholesterol esterification in cultured parenchymal cells and isolated microsomes from rat liver. , 1988, The Journal of biological chemistry.

[9]  T. Flatmark,et al.  Effect of a high-fat diet with partially hydrogenated fish oil on long-chain fatty acid metabolizing enzymes in subcellular fractions of rat liver. , 1987, Archives of biochemistry and biophysics.

[10]  R. Wanders,et al.  Acyl-CoA:dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method. , 1986, Biochimica et biophysica acta.

[11]  R. Boston,et al.  Suppression by diets rich in fish oil of very low density lipoprotein production in man. , 1984, The Journal of clinical investigation.

[12]  T. Flatmark,et al.  Enhancement of long-chain acyl-CoA hydrolase activity in peroxisomes and mitochondria of rat liver by peroxisomal proliferators. , 1984, European journal of biochemistry.

[13]  R. Wanders,et al.  Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome. , 1984, Biochemical and biophysical research communications.

[14]  S. Wong,et al.  The adaptive effects of dietary fish and safflower oil on lipid and lipoprotein metabolism in perfused rat liver. , 1984, Biochimica et biophysica acta.

[15]  R. Berge,et al.  Changes in lipid metabolizing enzymes of hepatic subcellular fractions from rats treated with tiadenol and clofibrate. , 1981, Biochemical pharmacology.

[16]  T. Flatmark,et al.  Polydispersity of rat liver peroxisomes induced by the hypolipidemic and carcinogenic agent clofibrate. , 1981, European journal of cell biology.

[17]  C. Drevon,et al.  Regulation of cholesterol esterification and biosynthesis in monolayer cultures of normal adult rat hepatocytes. , 1980, The Journal of biological chemistry.

[18]  A. Hajra,et al.  Properties of guinea pig liver peroxisomal dihydroxyacetone phosphate acyltransferase. , 1980, The Journal of biological chemistry.

[19]  R. Coleman,et al.  Triacylglycerol synthesis in isolated fat cells. Studies on the microsomal diacylglycerol acyltransferase activity using ethanol-dispersed diacylglycerols. , 1976, The Journal of biological chemistry.

[20]  J. Folch,et al.  A simple method for the isolation and purification of total lipides from animal tissues. , 1957, The Journal of biological chemistry.