A heteroplasmic, not homoplasmic, mitochondrial DNA mutation promotes tumorigenesis via alteration in reactive oxygen species generation and apoptosis

By Park Jeong Soon   Sharma Lokendra Kumar   Li Hongzhi   Xiang Ruihua   Holstein Deborah   Wu Jun   Lechleiter James   Naylor Susan L.   Deng Janice J.   Lu Jianxin   Bai Yidong  

Human Molecular Genetics, Vol. 18, Iss. 9, 2009-05 ,pp. : 1578-1589

Oxford University Press

Access to resources Recommend Favorite

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

Oxford University Press

Access to resources Recommend Favorite

Relationship of Genotype to Phenotype in Fibroblast-derived Transmitochondrial Cell Lines Carrying the 3243 Mutation Associated with the Melas Encephalomyopathy: Shift towards Mutant Genotype and Role of mtDNA Copy Number

By Bentlage Herman A. C. M.   Attardi Giuseppe  

Human Molecular Genetics, Vol. 5, Iss. 2, 1996-01 ,pp. : 197-205

Oxford University Press

Access to resources Recommend Favorite

A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1342-1348

John Wiley & Sons Inc

Access to resources Recommend Favorite

Molecular Phenotype of a Human Lymphoblastoid Cell-line Homoplasmic for the np 7445 Deafness-associated Mitochondrial Mutation

By Reid Fiona M.   Rovio Anja   Holt Ian J.   Jacobs Howard T.  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 443-449

Oxford University Press

Access to resources Recommend Favorite