Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophy
Author:
Funder
European Leukodystrophy Association
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/142500/files/pdf
Reference88 articles.
1. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
2. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters
3. Impaired Very Long-chain Acyl-CoA β-Oxidation in Human X-linked Adrenoleukodystrophy Fibroblasts Is a Direct Consequence of ABCD1 Transporter Dysfunction
4. Adrenoleukodystrophy: Impaired Oxidation of Very Long Chain Fatty Acids in White Blood Cells, Cultured Skin Fibroblasts, and Amniocytes
5. Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
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