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2. A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy. Heinzer AK; Watkins PA; Lu JF; Kemp S; Moser AB; Li YY; Mihalik S; Powers JM; Smith KD Hum Mol Genet; 2003 May; 12(10):1145-54. PubMed ID: 12719378 [TBL] [Abstract][Full Text] [Related]
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10. Metformin-induced mitochondrial function and ABCD2 up-regulation in X-linked adrenoleukodystrophy involves AMP-activated protein kinase. Singh J; Olle B; Suhail H; Felicella MM; Giri S J Neurochem; 2016 Jul; 138(1):86-100. PubMed ID: 26849413 [TBL] [Abstract][Full Text] [Related]
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12. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. Corzo D; Gibson W; Johnson K; Mitchell G; LePage G; Cox GF; Casey R; Zeiss C; Tyson H; Cutting GR; Raymond GV; Smith KD; Watkins PA; Moser AB; Moser HW; Steinberg SJ Am J Hum Genet; 2002 Jun; 70(6):1520-31. PubMed ID: 11992258 [TBL] [Abstract][Full Text] [Related]
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20. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters. van Roermund CW; Visser WF; Ijlst L; van Cruchten A; Boek M; Kulik W; Waterham HR; Wanders RJ FASEB J; 2008 Dec; 22(12):4201-8. PubMed ID: 18757502 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]