mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae

By Stumpf Jeffrey D.   Bailey Christopher M.   Spell Diana   Stillwagon Matthew   Anderson Karen S.   Copeland William C.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2123-2133

Oxford University Press

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Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase  associated with progressive external ophthalmoplegia

By Stuart Gregory R.   Santos Janine H.   Strand Micheline K.   Van Houten Bennett   Copeland William C.  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 363-374

Oxford University Press

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Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans

By Baruffini Enrico   Lodi Tiziana   Puglisi Andrea   Zeviani Massimo   Ferrero Iliana  

Human Molecular Genetics, Vol. 15, Iss. 19, 2006-10 ,pp. : 2846-2855

Oxford University Press

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PGC-1/ upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutations

By Srivastava Sarika   Barrett John N.   Moraes Carlos T.  

Human Molecular Genetics, Vol. 16, Iss. 8, 2007-04 ,pp. : 993-1005

Oxford University Press

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The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1

By Antonicka Hana   Sasarman Florin   Kennaway Nancy G.   Shoubridge Eric A.  

Human Molecular Genetics, Vol. 15, Iss. 11, 2006-06 ,pp. : 1835-1846

Oxford University Press

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