Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

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Human Molecular Genetics, Vol. 15, Iss. 13, 2006-07 ,pp. : 2076-2086

Oxford University Press

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Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families

By Brown Michael   Zhadanov Sergei   Allen Jon   Hosseini Seyed   Newman Nancy   Atamonov Vasily   Mikhailovskaya Irina   Sukernik Rem   Wallace Douglas  

Human Genetics, Vol. 109, Iss. 1, 2001-07 ,pp. : 33-39

Springer Publishing Company

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High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer’s disease brain

By Simon D.K.   Lin M.T.   Ahn C.H.   Kim L.M.   Beal M.F.  

Human Molecular Genetics, Vol. 11, Iss. 2, 2002-01 ,pp. : 133-145

Oxford University Press

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Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition

By Gilkerson Robert W.   De Vries Rosa L.A.   Lebot Paul   Wikstrom Jakob D.   Torgyekes Edina   Shirihai Orian S.   Przedborski Serge   Schon Eric A.  

Human Molecular Genetics, Vol. 21, Iss. 5, 2012-03 ,pp. : 978-990

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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

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Oxford University Press

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