The chemical biology of branched-chain lipid metabolism
- 1 September 2003
- journal article
- review article
- Published by Elsevier in Progress in Lipid Research
- Vol. 42 (5) , 359-376
- https://doi.org/10.1016/s0163-7827(03)00016-x
Abstract
No abstract availableKeywords
This publication has 124 references indexed in Scilit:
- Kinetic and crystallographic studies on deacetoxycephalosporin C synthase (DAOCS)Journal of Molecular Biology, 2001
- Human Very-Long-Chain Acyl-CoA Synthetase: Cloning, Topography, and Relevance to Branched-Chain Fatty Acid MetabolismBiochemical and Biophysical Research Communications, 1999
- Studies on the active site of deacetoxycephalosporin C synthaseJournal of Molecular Biology, 1999
- Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase geneNature Genetics, 1997
- Identification of PAHX, a Refsum disease geneNature Genetics, 1997
- Fatty Acid β-Oxidation in Peroxisomes and Mitochondria: The First, Unequivocal Evidence for the Involvement of Carnitine in Shuttling Propionyl-CoA from Peroxisomes to MitochondriaBiochemical and Biophysical Research Communications, 1995
- Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liverBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1992
- Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomesBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1992
- Metabolic stereoisomeric inversion of ibuprofen in mammalsBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1991
- The existence of an alternative pathway for the degradation of branch-chained fatty acids, and its failure in heredopathia atactica polyneuriti-formis (Refsum's disease)Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1966