| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 16060290 | 2005 | Guo, L. J., Oshida, Y., Fuku, N., Takeyasu, T., Fujita, Y., Kurata, M., Sato, Y., Ito, M., Tanaka, M. (2005) Mitochondrial genome polymorphisms associated with type-2 diabetes or obesity Mitochondrion . 5 (1): 15-33 . |
| 2 | 16431939 | 2006 | Qu, J., Li, R., Zhou, X., Tong, Y., Lu, F., Qian, Y., Hu, Y., Mo, J. Q., West, C. E., Guan, M. X. (2006) The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation Investigative Ophthalmology and Visual Science . 47 (2): 475-483 . |
| 3 | 17123466 | 2007 | Bandelt, H. J., Yao, Y. G., Salas, A., Kivisild, T., Bravi, C. M. (2007) High penetrance of sequencing errors and interpretative shortcomings in mtDNA sequence analysis of LHON patients Biochemical and Biophysical Research Communications . 352 (2): 283-291 . |
| 4 | 19022198 | 2008 | Cai, W., Fu, Q., Zhou, X., Qu, J., Tong, Y., Guan, M. X. (2008) Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation Journal of Genetics and Genomics . 35 (11): 649-655 . |
| 5 | 19398658 | 2009 | Liu, Y., Li, R., Li, Z., Wang, X. J., Yang, L., Wang, S., Guan, M. X. (2009) Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree Hypertension . 53 (6): 1083-1090 . |
| 6 | 19778529 | 2009 | Zhu, H. Y., Wang, S. W., Liu, L., Chen, R., Wang, L., Gong, X. L., Zhang, M. L. (2009) Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population Clinica Chimica Acta . 410 (40545): 64-69 . |
| 7 | 21694735 | 2011 | Lu, Z., Chen, H., Meng, Y., Wang, Y., Xue, L., Zhi, S., Qiu, Q., Yang, L., Mo, J. Q., Guan, M. X. (2011) The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree European Journal of Human Genetics . 19 (11): 1181-1186 . |
| 8 | 27214402 | 2016 | Nakano, S., Suzuki, T., Kawarada, L., Iwata, H., Asano, K., Suzuki, T. (2016) NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNA(Met) Nature Chemical Biology . 12 (7): 546-551 . |
| 9 | 29211511 | 2018 | Zheng, P., Li, S., Liu, C., Zha, Z., Wei, X., Yuan, Y. (2018) Mitochondrial tRNA(Ala) C5601T mutation may modulate the clinical expression of tRNA(Met) A4435G mutation in a Han Chinese family with hypertension Clinical and Experimental Hypertension . 40 (6): 595-600 . |
| 10 | 29222331 | 2018 | Zhou, M., Xue, L., Chen, Y., Li, H., He, Q., Wang, B., Meng, F., Wang, M., Guan, M. X. (2018) A hypertension-associated mitochondrial DNA mutation introduces an m(1)G37 modification into tRNA(Met), altering its structure and function The Journal of Biological Chemistry . 293 (4): 1425-1438 . |
| 11 | 29340697 | 2018 | Valiente-Palleja, A., Torrell, H., Muntane, G., Cortes, M. J., Martinez-Leal, R., Abasolo, N., Alonso, Y., Vilella, E., Martorell, L. (2018) Genetic and clinical evidence of mitochondrial dysfunction in autism spectrum disorder and intellectual disability Human Molecular Genetics . 27 (5): 891-900 . |
| 12 | 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 . |
| 13 | 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 . |
| 14 | 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 . |
| 15 | 34755158 | 2021 | Podskoczyj, K., Kulik, K., Wasko, J., Nawrot, B., Suzuki, T., Leszczynska, G. (2021) Synthesis and properties of the anticodon stem-loop of human mitochondrial tRNA(Met) containing the disease-related G or m(1)G nucleosides at position 37 Chemical Communications (Cambridge, England) . 57 (93): 12540-12543 . |
| 16 | 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 . |
| 17 | 34120304 | 2022 | Finsterer, J. (2022) tRNA variants causing Leber's hereditary optic neuropathy? Irish Journal of Medical Science . 191 (3): 1443-1444 . |