| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 27536005 | 2016 | Wang, M., Peng, Y., Zheng, J., Zheng, B., Jin, X., Liu, H., Wang, Y., Tang, X., Huang, T., Jiang, P., Guan, M. X. (2016) A deafness-associated tRNA Asp mutation alters the m1G37 modification, aminoacylation and stability of tRNA Asp and mitochondrial function Nucleic Acids Research . 44 (22): 10974-10985 . |
| 2 | 27544295 | 2016 | Xue, L., Wang, M., Li, H., Wang, H., Jiang, F., Hou, L., Geng, J., Lin, Z., Peng, Y., Zhou, H., Yu, H., Jiang, P., Mo, J. Q., Guan, M. X. (2016) Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension Mitochondrion . 30 (): 208-21 . |
| 3 | 30592262 | 2019 | Zhang, J., Lu, B., Xia, W. W., Fang, B., Ding, X. X., Hu, G. W. (2019) The mitochondrial transfer RNAAsp A7551G mutation may contribute to the clinical expression of deafness associated with the A1555G mutation in a pedigree with hearing impairment Molecular Medicine Reports . 19 (3): 1797-1802 . |
| 4 | 32169613 | 2020 | Zheng, J., Bai, X., Xiao, Y., Ji, Y., Meng, F., Aishanjiang, M., Gao, Y., Wang, H., Fu, Y., Guan, M. X. (2020) Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss Mitochondrion . 52 (): 163-172 . |