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Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders.
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Demonstration of dimethylnonanoyl-CoA thioesterase activity in rat liver peroxisomes followed by purification and molecular cloning of the thioesterase involved.
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Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling.
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Identification of pristanal dehydrogenase activity in peroxisomes: Conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes.
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Subcellular localization and physiological role of alpha-methylacyl-CoA racemase.
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Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx): activity measurements in liver and fibroblasts using a newly developed method.
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Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.
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Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution.
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Molecular cloning and expression of human carnitine octanoyltransferase: Evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids.
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Diagnosis and follow-up of a case of peroxisomal disorder with peroxisomal mosaicism.