Frataxin deficiency enhances apoptosis in cells differentiating into neuroectoderm

By Santos M.M.   Ohshima K.   Pandolfo M.  

Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1935-1944

Oxford University Press

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Frataxin expression rescues mitochondrial dysfunctions in FRDA cells

By Lonnerdal B.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2099-2107

Oxford University Press

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Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

By Antonicka Hana  

Human Molecular Genetics, Vol. 12, Iss. 20, 2003-10 ,pp. : 2693-2702

Oxford University Press

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Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR pathway as a therapeutic target in Friedreichs ataxia

By Coppola Giovanni   Marmolino Daniele   Lu Daning   Wang Qing   Cnop Miriam   Rai Myriam   Acquaviva Fabio   Cocozza Sergio   Pandolfo Massimo   Geschwind Daniel H.  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2452-2461

Oxford University Press

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A mutation in the human heme A:farnesyltransferase gene ( COX10 ) causes cytochrome c oxidase deficiency

By Valnot Isabelle   von Kleist-Retzow Jürgen-Christoph   Barrientos Antoni  

Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1245-1249

Oxford University Press

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