Human peroxisomal disorders
Author:
Publisher
Wiley
Subject
Medical Laboratory Technology,Instrumentation,Histology,Anatomy
Reference225 articles.
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4. Inactivation of the Peroxisomal Multifunctional Protein-2 in Mice Impedes the Degradation of Not Only 2-Methyl-branched Fatty Acids and Bile Acid Intermediates but Also of Very Long Chain Fatty Acids
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1. Protective effect of oleic acid against very long-chain fatty acid-induced apoptosis in peroxisome-deficient CHO cells;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2024-04
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4. SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders;Acta Neuropathologica;2023-05-15
5. Peroxisomes attenuate cytotoxicity of very long-chain fatty acids;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2023-02
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