Introduction of heteroplasmic mitochondrial DNA (mtDNA) from a patient with NARP into two human ° cell lines is associated either with selection and maintenance of NARP mutant mtDNA or failure to maintain mtDNA

By Vergani L.   Rossi R.   Brierley C. H.  

Human Molecular Genetics, Vol. 8, Iss. 9, 1999-09 ,pp. : 1751-1755

Oxford University Press

Access to resources Recommend Favorite

Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA

By Geromel V.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1221-1228

Oxford University Press

Access to resources Recommend Favorite

Introducing the human Leigh syndrome mutation T9176G into Saccharomyces cerevisiae mitochondrial DNA leads to severe defects in the incorporation of Atp6p into the ATP synthase and in the mitochondrial morphology

By Kucharczyk Roza   Salin Bndicte   di Rago J.-P.  

Human Molecular Genetics, Vol. 18, Iss. 15, 2009-08 ,pp. : 2889-2898

Oxford University Press

Access to resources Recommend Favorite

Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA

By Malena Adriana   Loro Emanuele   Di Re Miriam   Holt Ian J.   Vergani Lodovica  

Human Molecular Genetics, Vol. 18, Iss. 18, 2009-09 ,pp. : 3407-3416

Oxford University Press

Access to resources Recommend Favorite

Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice

By Lloret Alejandro   Dragileva Ella   Teed Allison   Espinola Janice   Fossale Elisa   Gillis Tammy   Lopez Edith   Myers Richard H.   MacDonald Marcy E.   Wheeler Vanessa C.  

Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. : 2015-2024

Oxford University Press

Access to resources Recommend Favorite