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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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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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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Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage

By Ferrer Isidre   Kapfhammer Josef P.   Hindelang Colette   Kemp Stephan   Troffer-Charlier Nathalie   Broccoli Vania   Callyzot Noëlle   Mooyer Petra   Selhorst Jacqueline   Vreken Peter   Wanders Ronald J.A.   Mandel Jean Louis   Pujol Aurora  

Human Molecular Genetics, Vol. 14, Iss. 23, 2005-12 ,pp. : 3565-3577

Oxford University Press

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Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins

By Spencer Corinne M.   Serysheva Ekaterina   Yuva-Paylor Lisa A.   Oostra Ben A.   Nelson David L.   Paylor Richard  

Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. : 1984-1994

Oxford University Press

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