Acquisition of the wobble modification in mitochondrial tRNA Leu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect

By Kirino Yohei   Yasukawa Takehiro   Marjavaara Sanna K.   Jacobs Howard T.   Holt Ian J.   Watanabe Kimitsuna   Suzuki Tsutomu  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 897-904

Oxford University Press

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Mitochondrial tRNA Leu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation

By El Meziane A.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2141-2147

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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Metabolic consequences of a novel missense mutation of the mtDNA CO I gene

By Heils A.  

Human Molecular Genetics, Vol. 11, Iss. 16, 2002-08 ,pp. : 1797-1805

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A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome

By Tiranti Valeria   Corona Paola   Greco Marilena   Taanman Jan-Willem  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2733-2742

Oxford University Press

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