Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation
Jing Wang(Hebei Agricultural University), Min‐Xin Guan(Zhejiang University)
Cited by 14
Related Papers
A deafness-associated tRNA<sup>His</sup>mutation alters the mitochondrial function, ROS production and membrane potential
|Nucleic Acids Research|2014|114
The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation
|Human Molecular Genetics|2015|103
A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction
|Journal of Biological Chemistry|2016|82
A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function
|Journal of Biological Chemistry|2017|68
A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis
|Nucleic Acids Research|2018|68