Index | PMID | Date | Reference |
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1 | 9344764 | 1997 | Li, Y. Y., Maisch, B., Rose, M. L., Hengstenberg, C. (1997) Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy Journal of Molecular and Cellular Cardiology . 29 (10): 2699-2709 . |
2 | 20153673 | 2010 | Tang, X., Li, R., Zheng, J., Cai, Q., Zhang, T., Gong, S., Zheng, W., He, X., Zhu, Y., Xue, L., Yang, A., Yang, L., Lu, J., Guan, M. X. (2010) Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family Molecular Genetics and Metabolism . 100 (1): 57-64 . |
3 | 22538251 | 2012 | Zheng, J., Ji, Y., Guan, M. X. (2012) Mitochondrial tRNA mutations associated with deafness Mitochondrion . 12 (3): 406-413 . |
4 | 25968158 | 2015 | Tang, X., Zheng, J., Ying, Z., Cai, Z., Gao, Y., He, Z., Yu, H., Yao, J., Yang, Y., Wang, H., Chen, Y., Guan, M. X. (2015) Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss Mitochondrion . 23 (): 17-24 . |
5 | 28990081 | 2017 | Ji, Y., Qiao, L., Liang, X., Zhu, L., Gao, Y., Zhang, J., Jia, Z., Wei, Q. P., Liu, X., Jiang, P., Guan, M. X. (2017) Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigrees Molecular Medicine Reports . 16 (6): 8997-9004 . |
6 | 30783460 | 2019 | Lin, L., Cui, P., Qiu, Z., Wang, M., Yu, Y., Wang, J., Sun, Q., Zhao, H. (2019) The mitochondrial tRNA(Ala) 5587T>C and tRNA(Leu(CUN)) 12280A>G mutations may be associated with hypertension in a Chinese family Experimental and Therapeutic Medicine 17 (3): 1855-1862 . |
7 | 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 . |
8 | 33552719 | 2021 | Ding, Y., Zhuo, G., Guo, Q., Li, M. (2021) Leber's hereditary optic neuropathy: the roles of mitochondrial transfer RNA variants PeerJ . 9 (): e10651 . |
9 | 34023389 | 2021 | Ji, Y., Nie, Z., Meng, F., Hu, C., Chen, H., Jin, L., Chen, M., Zhang, M., Zhang, J., Liang, M., Wang, M., Guan, M. X. (2021) Mechanistic insights into mitochondrial tRNA(Ala) 3'-end metabolism deficiency The Journal of Biological Chemistry . 297 (1): 100816 . |
10 | 34053002 | 2022 | Shuai, J., Shi, J., Liang, Y., Ji, F., Gu, L., Yuan, Z. (2022) Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber's hereditary optic neuropathy Irish Journal of Medical Science 191 (2): 865-876 . |
11 | 34120304 | 2022 | Finsterer, J. (2022) tRNA variants causing Leber's hereditary optic neuropathy? Irish Journal of Medical Science . 191 (3): 1443-1444 . |