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

By Kong Qing-Peng   Bandelt Hans-Jürgen   Sun Chang   Yao Yong-Gang   Salas Antonio   Achilli Alessandro   Wang Cheng-Ye   Zhong Li   Zhu Chun-Ling   Wu Shi-Fang   Torroni Antonio   Zhang Ya-Ping  

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

Oxford University Press

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The relationship between somatic mtDNA rearrangements, human heart disease and aging

By Kajander O.A.  

Human Molecular Genetics, Vol. 11, Iss. 3, 2002-02 ,pp. : 317-324

Oxford University Press

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Increased mitochondrial biogenesis in muscle improves aging phenotypes in the mtDNA mutator mouse

By Dillon Lloye M.   Williams Siôn L.   Hida Aline   Peacock Jacqueline D.   Prolla Tomas A.   Lincoln Joy   Moraes Carlos T.  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2288-2297

Oxford University Press

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Spectrum of pathogenic mtDNA mutations in Leber’s hereditary optic neuropathy families from Siberia

By Volodko N.   L’vova M.   Starikovskaya E.   Derbeneva O.   Bychkov I.   Mikhailovskaya I.   Pogozheva I.   Fedotov F.   Soyan G.   Procaccio V.   Wallace D.   Sukernik R.  

Russian Journal of Genetics, Vol. 42, Iss. 1, 2006-01 ,pp. : 76-83

MAIK Nauka/Interperiodica

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Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria

By Temperley R.J.  

Human Molecular Genetics, Vol. 12, Iss. 18, 2003-09 ,pp. : 2341-2348

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