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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Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy

By Asheuer Muriel  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1293-1303

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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Adrenoleukodystrophy‐related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X‐ALD): implications for therapy

By Netik Angela   Forss‐Petter Sonja   Holzinger Andreas   Molzer Brunhilde   Unterrainer Gertraud   Berger Johannes  

Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 907-913

Oxford University Press

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