Index | PMID | Date | Reference |
---|---|---|---|
1 | 25615420 | 2015 | Liu, H., Li, R., Li, W., Wang, M., Ji, J., Zheng, J., Mao, Z., Mo, J. Q., Jiang, P., Lu, J., Guan, M. X. (2015) Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene Mitochondrion . 21 (): 49-57 . |
2 | 26134044 | 2015 | Li, W., Wen, C., Li, W., Wang, H., Guan, X., Zhang, W., Ye, W., Lu, J. (2015) The tRNA(Gly) T10003C mutation in mitochondrial haplogroup M11b in a Chinese family with diabetes decreases the steady-state level of tRNA(Gly), increases aberrant reactive oxygen species production, and reduces mitochondrial membrane potential Molecular and Cellular Biochemistry 408 (1-2): 171-179 . |
3 | 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 . |
4 | 31965079 | 2020 | Wong, L. C., Chen, T., Wang, J., Tang, S., Schmitt, E. S., Landsverk, M., Li, F., Wang, Y., Zhang, S., Zhang, V. W., Craigen, W. J. (2020) Interpretation of mitochondrial tRNA variants Genetics in Medicine 22 (5): 917-926; Suppl Table 1 . |
5 | 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 . |