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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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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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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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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Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28

By Gigarel Nadine   Frydman Nelly   Burlet Philippe   Kerbrat Violaine   Steffann Julie   Frydman René   Munnich Arnold   Ray Pierre  

Human Genetics, Vol. 114, Iss. 3, 2004-02 ,pp. : 298-305

Springer Publishing Company

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