Progressive loss of mitochondrial DNA in thymidine kinase 2-deficient mice

By Zhou Xiaoshan   Solaroli Nicola   Bjerke Mia   Stewart James B.   Rozell Bjrn   Johansson Magnus   Karlsson Anna  

Human Molecular Genetics, Vol. 17, Iss. 15, 2008-08 ,pp. : 2329-2335

Oxford University Press

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Dominant membrane uncoupling by mutant adenine nucleotide translocase in mitochondrial diseases

By Wang Xiaowen   Salinas Kelly   Zuo Xiaoming   Kucejova Blanka   Chen Xin Jie  

Human Molecular Genetics, Vol. 17, Iss. 24, 2008-12 ,pp. : 4036-4044

Oxford University Press

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The DNA translocase activity of FANCM protects stalled replication forks

By Blackford Andrew N.   Schwab Rebekka A.   Nieminuszczy Jadwiga   Deans Andrew J.   West Stephen C.   Niedzwiedz Wojciech  

Human Molecular Genetics, Vol. 21, Iss. 9, 2012-05 ,pp. : 2005-2016

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

Oxford University Press

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The mitochondrial protein frataxin prevents nuclear damage

By Karthikeyan G.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1351-1362

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