Functional analysis of human MLH1 and MSH2 missense variants and hybrid human–yeast MLH1 proteins in Saccharomyces cerevisiae

By Ellison A.R.   Lofing J.   Bitter G.A.  

Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1889-1900

Oxford University Press

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Characterization of Missense Mutations in the SUP45 Gene of Saccharomyces cerevisiae Encoding Translation Termination Factor eRF1*

By Moskalenko S. E.   Zhouravleva G. A.   Soom M. Y.   Chabelskaya S. V.   Volkov K. V.   Zemlyanko O. M.   Philippe M.   Mironova L. N.   Inge-Vechtomov S. G.  

Russian Journal of Genetics, Vol. 40, Iss. 5, 2004-05 ,pp. : 478-484

MAIK Nauka/Interperiodica

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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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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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Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis

By Alazzouzi Hafid  

Human Molecular Genetics, Vol. 14, Iss. 2, 2005-01 ,pp. : 235-239

Oxford University Press

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