Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans

By Srivastava Sarika   Moraes Carlos T.  

Human Molecular Genetics, Vol. 14, Iss. 7, 2005-04 ,pp. : 893-902

Oxford University Press

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Mitochondrial transcription factor A regulates mtDNA copy number in mammals

By Ekstrand Mats I.   Falkenberg Maria   Rantanen Anja   Park Chan Bae   Gaspari Martina   Hultenby Kjell   Rustin Pierre   Gustafsson Claes M.   Larsson Nils-Göran  

Human Molecular Genetics, Vol. 13, Iss. 9, 2004-05 ,pp. : 935-944

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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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

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A Novel Heteroplasmic tRNA leu(CUN) mtDNA Point Mutation in a Sporadic Patient With Mitochondrial Encephalomyopathy Segregates Rapidly in Skeletal Muscle and Suggests an Approach to Therapy

By Fu Katherine   Hartlen Rebecca   Johns Timothy   Genge Angela   Karpati George   Shoubridge Eric A.  

Human Molecular Genetics, Vol. 5, Iss. 11, 1996-11 ,pp. : 1835-1840

Oxford University Press

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