MITOMAP References for RNA Mutation T5587C

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Index PMID Date Reference
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 .