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Journal Abstract Search

316 related items for PubMed ID: 16368709

  • 1. Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase gamma associated with progressive external ophthalmoplegia.
    Stuart GR, Santos JH, Strand MK, Van Houten B, Copeland WC.
    Hum Mol Genet; 2006 Jan 15; 15(2):363-74. PubMed ID: 16368709
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  • 2. Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans.
    Baruffini E, Lodi T, Dallabona C, Puglisi A, Zeviani M, Ferrero I.
    Hum Mol Genet; 2006 Oct 01; 15(19):2846-55. PubMed ID: 16940310
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  • 3. mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae.
    Stumpf JD, Bailey CM, Spell D, Stillwagon M, Anderson KS, Copeland WC.
    Hum Mol Genet; 2010 Jun 01; 19(11):2123-33. PubMed ID: 20185557
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  • 4. Mitochondrial DNA defects in Saccharomyces cerevisiae caused by functional interactions between DNA polymerase gamma mutations associated with disease in human.
    Baruffini E, Ferrero I, Foury F.
    Biochim Biophys Acta; 2007 Dec 01; 1772(11-12):1225-35. PubMed ID: 17980715
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  • 11. A cluster of pathogenic mutations in the 3'-5' exonuclease domain of DNA polymerase gamma defines a novel module coupling DNA synthesis and degradation.
    Szczepanowska K, Foury F.
    Hum Mol Genet; 2010 Sep 15; 19(18):3516-29. PubMed ID: 20601675
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  • 12. The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders.
    Cohen BH, Naviaux RK.
    Methods; 2010 Aug 15; 51(4):364-73. PubMed ID: 20558295
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  • 13. Mutations in AAC2, equivalent to human adPEO-associated ANT1 mutations, lead to defective oxidative phosphorylation in Saccharomyces cerevisiae and affect mitochondrial DNA stability.
    Fontanesi F, Palmieri L, Scarcia P, Lodi T, Donnini C, Limongelli A, Tiranti V, Zeviani M, Ferrero I, Viola AM.
    Hum Mol Genet; 2004 May 01; 13(9):923-34. PubMed ID: 15016764
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  • 19. MMS exposure promotes increased MtDNA mutagenesis in the presence of replication-defective disease-associated DNA polymerase γ variants.
    Stumpf JD, Copeland WC.
    PLoS Genet; 2014 Oct 01; 10(10):e1004748. PubMed ID: 25340760
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  • 20. Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations.
    Kollberg G, Jansson M, Pérez-Bercoff A, Melberg A, Lindberg C, Holme E, Moslemi AR, Oldfors A.
    Eur J Hum Genet; 2005 Apr 01; 13(4):463-9. PubMed ID: 15702133
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