Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy

By Unterrainer Gertraud   Molzer Brunhilde   Forss-Petter Sonja   Berger Johannes  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2609-2616

Oxford University Press

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Cholesterol regulates ABCD2 expression: implications for the therapy of X-linked adrenoleukodystrophy

By Weinhofer Isabelle   Forss-Petter Sonja   Žigman Mihaela   Berger Johannes  

Human Molecular Genetics, Vol. 11, Iss. 22, 2002-10 ,pp. : 2701-2708

Oxford University Press

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Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency

By Oezen Iris  

Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1127-1137

Oxford University Press

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Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy

By Pujol Aurora  

Human Molecular Genetics, Vol. 13, Iss. 23, 2004-12 ,pp. : 2997-3006

Oxford University Press

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Valproic acid induces antioxidant effects in X-linked adrenoleukodystrophy

By Fourcade Stphane   Ruiz Montserrat   Guilera Cristina   Hahnen Eric   Brichta Lars   Naudi Alba   Portero-Otn Manuel   Dacremont Georges   Cartier Nathalie   Wanders Ronald   Kemp Stephan   Mandel Jean Louis   Wirth Brunhilde   Pamplona Reinald   Aubourg Patrick   Pujol Aurora  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 2005-2014

Oxford University Press

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