Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomes
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry,Biophysics
Reference18 articles.
1. Über das Vorkommen der 3.7.11.15-Tetramethyl-hexadecansäure (Phytansäure) in den Cholesterinestern und anderen Lipoidfraktionen der Organe bei einem Krankheitsfall unbekannter Genese (Verdacht auf Heredopathia atactica polyneuritiformis [Refsum-Syndrom])
2. Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction
3. Pristanic acid and phytanic acid in plasma from patients with a single peroxisomal enzyme deficiency
4. Peroxisomal disorders in neurology
5. The Metabolic Basis of Inherited Disease;Steinberg,1989
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1. The chemical biology of branched-chain lipid metabolism;Progress in Lipid Research;2003-09
2. Role and Organization of Peroxisomal β-Oxidation;Current Views of Fatty Acid Oxidation and Ketogenesis;2002
3. Peroxisomes, Lipid Metabolism, and Human Disease;Cell Biochemistry and Biophysics;2000
4. Phytanic acid α-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomes;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;1999-09
5. Lipid metabolism in peroxisomes in relation to human disease;Molecular Aspects of Medicine;1998-04
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