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1030 related items for PubMed ID: 9326946

  • 1. Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
    Rötig A, de Lonlay P, Chretien D, Foury F, Koenig M, Sidi D, Munnich A, Rustin P.
    Nat Genet; 1997 Oct; 17(2):215-7. PubMed ID: 9326946
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  • 2. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
    Puccio H, Simon D, Cossée M, Criqui-Filipe P, Tiziano F, Melki J, Hindelang C, Matyas R, Rustin P, Koenig M.
    Nat Genet; 2001 Feb; 27(2):181-6. PubMed ID: 11175786
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  • 3. Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue.
    Wilson RB, Roof DM.
    Nat Genet; 1997 Aug; 16(4):352-7. PubMed ID: 9241271
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  • 5. Friedreich ataxia: the oxidative stress paradox.
    Seznec H, Simon D, Bouton C, Reutenauer L, Hertzog A, Golik P, Procaccio V, Patel M, Drapier JC, Koenig M, Puccio H.
    Hum Mol Genet; 2005 Feb 15; 14(4):463-74. PubMed ID: 15615771
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  • 7. Iron-sulfur protein maturation in human cells: evidence for a function of frataxin.
    Stehling O, Elsässer HP, Brückel B, Mühlenhoff U, Lill R.
    Hum Mol Genet; 2004 Dec 01; 13(23):3007-15. PubMed ID: 15509595
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  • 9. Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae.
    Cavadini P, Gellera C, Patel PI, Isaya G.
    Hum Mol Genet; 2000 Oct 12; 9(17):2523-30. PubMed ID: 11030757
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  • 13. Glutathione-dependent redox status of frataxin-deficient cells in a yeast model of Friedreich's ataxia.
    Auchère F, Santos R, Planamente S, Lesuisse E, Camadro JM.
    Hum Mol Genet; 2008 Sep 15; 17(18):2790-802. PubMed ID: 18562474
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  • 16. Mitochondrial dysfunction in friedreich's ataxia.
    Lodi R, Taylor DJ, Schapira AH.
    Biol Signals Recept; 2001 Sep 15; 10(3-4):263-70. PubMed ID: 11351132
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