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, Xiaofen Jin 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, Jing Zheng et al.|Journal of Biological Chemistry|2016Cited by 82
A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesisZidong Jia, Min‐Xin Guan, Ye Zhang et al.|Nucleic Acids Research|2018Cited by 68
A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and functionMi Zhou, Min‐Xin Guan, Ling Xue et al.|Journal of Biological Chemistry|2017Cited by 68