Role of very-long-chain acyl-coenzyme A synthetase in X-linked adrenoleukodystrophy
- 1 September 1999
- journal article
- research article
- Published by Wiley in Annals of Neurology
- Vol. 46 (3) , 409-412
- https://doi.org/10.1002/1531-8249(199909)46:3<409::aid-ana18>3.0.co;2-9
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Human Very-Long-Chain Acyl-CoA Synthetase: Cloning, Topography, and Relevance to Branched-Chain Fatty Acid MetabolismBiochemical and Biophysical Research Communications, 1999
- X-Linked Adrenoleukodystrophy: Genes, Mutations, and PhenotypesNeurochemical Research, 1999
- Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteinsHuman Molecular Genetics, 1998
- Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transportersNature, 1993
- Peroxisomal fatty acid β-oxidation in HepG2 cellsArchives of Biochemistry and Biophysics, 1991
- Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy.Proceedings of the National Academy of Sciences, 1988
- Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acidsBiochemical and Biophysical Research Communications, 1988
- Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.Proceedings of the National Academy of Sciences, 1984
- AdrenoleukodystrophyNeurology, 1981
- Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblastsAnnals of Neurology, 1980