Index | PMID | Date | Reference |
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1 | 8728098 | 1996 | Sawano, T., Tanaka, M., Ohno, K., Yoneda, M., Ota, Y., Terasaki, H., Awaya, S., Ozawa, T. (1996) Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease Biochemistry and Molecular Biology International (Sydney) . 38 (4): 693-700 . |
2 | 27519417 | 2016 | Wang, M., Liu, H., Zheng, J., Chen, B., Zhou, M., Fan, W., Wang, H., Liang, X., Zhou, X., Eriani, G., Jiang, P., Guan, M. X. (2016) A deafness- and diabetes-associated tRNA mutation causes deficient pseudouridinylation at position 55 in tRNAGlu and mitochondrial dysfunction The Journal of Biological Chemistry . 291 (40): 21029-21041 . |
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 | 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 . |
5 | 33289513 | 2020 | Jiang, P., Ling, Y., Zhu, T., Luo, X., Tao, Y., Meng, F., Cheng, W., Ji, Y. (2020) Mitochondrial tRNA mutations in Chinese children with tic disorders Bioscience Reports . 40 (12): BSR20201856 . |