A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy

By Heinzer Ann K.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1145-1154

Oxford University Press

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The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?

By Andresen Brage Storstein  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-05 ,pp. : 695-707

Oxford University Press

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Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders

By Djouadi F.  

Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2695-2703

Oxford University Press

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Functional Correction of Short-Chain Acyl-CoA Dehydrogenase Deficiency in Transgenic Mice: Implications for Gene Therapy of Human Mitochondrial Enzyme Deficiencies

By Kelly C. Lisa   Rhead William J.   Kutschke William K.   Brix Amy E.   Hamm Doug A.   Pinkert Carl A.   Lindsey J. Russell   Wood Philip A.  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1451-1455

Oxford University Press

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The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level

By Pedersen Christina  

Human Genetics, Vol. 124, Iss. 1, 2008-08 ,pp. : 43-56

Springer Publishing Company

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