A deafness-associated tRNA<sup>His</sup>mutation alters the mitochondrial function, ROS production and membrane potentialShasha Gong, Min‐Xin Guan, Yanyan Peng et al.|Nucleic Acids Research|2014Cited by 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 mutationPingping Jiang, Min‐Xin Guan, Meng Wang et al.|Human Molecular Genetics|2015Cited by 103
A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial DysfunctionMeng Wang, Min‐Xin Guan, Hao Liu et al.|Journal of Biological Chemistry|2016Cited by 82
PRICKLE3 linked to ATPase biogenesis manifested Leber’s hereditary optic neuropathyJialing Yu, Min‐Xin Guan, Xiaoyang Liang et al.|Journal of Clinical Investigation|2020Cited by 63
A Hypertension-Associated tRNA<sup>Ala</sup> Mutation Alters tRNA Metabolism and Mitochondrial FunctionPingping Jiang, Min‐Xin Guan, Meng Wang et al.|Molecular and Cellular Biology|2016Cited by 58