On the mechanism of the hypolipidemic effect of sulfur-substituted hexadecanedioic acid (3-thiadicarboxylic acid) in normolipidemic rats
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference40 articles.
1. Alkylthioacetic acids (3-thia fatty acids) as non-β-oxidizable fatty acid analogues: a new group of hypolipidemic drugs. III. Dissociation of cholesterol- and triglyceride-lowering effects and the induction of peroxisomal β-oxidation;Aarsland;J. Lipid Res.,1989
2. Alkylthioacetic acids (3-thia fatty acids) —a new group of non-β-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;Berge;Biochem. Pharmacol.,1989
3. Alkylthioacetic acids (3-thia fatty acids) —a new group of non-β-oxidizable peroxisome-inducing fatty acid analogues. I. A study on the structural requirements for proliferation of peroxisomes and mitochondria in rat liver;Berge;Biochim. Biophys. Acta.,1989
4. Regulation of fatty acid oxidation and triglyceride and phospholipid metabolism by hypolipidemic sulfur-substituted fatty acid analogues;Skorve;J. Lipid Res.,1990
5. Assembly and secretion of hepatic very-low-density lipoprotein;Gibbons;Biochem. J.,1990
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