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

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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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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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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Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues

By Bodyak N.D.   Nekhaeva E.   Wei J.Y.   Khrapko K.  

Human Molecular Genetics, Vol. 10, Iss. 1, 2001-01 ,pp. : 17-24

Oxford University Press

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