Index | PMID | Date | Reference |
---|---|---|---|
1 | 14571459 | 2003 | Tzen, C. Y., Thajeb, P., Wu, T. Y., Chen, S. C. (2003) Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g) Muscle and Nerve . 28 (5): 575-581 . |
2 | 16331560 | 2005 | Tang, D. L., Zhou, X., Zhou, K. Y., Li, X., Zhao, L., Liu, F., Zheng, F., Liu, S. M. (2005) [Association of mitochondrial DNA variation with type 2 diabetes mellitus] Zhonghua Yi Xue Yi Chuan Xue Za Zhi . 22 (6): 636-640 . |
3 | 16364244 | 2006 | Zhou, X., Wei, Q., Yang, L., Tong, Y., Zhao, F., Lu, C., Qian, Y., Sun, Y., Lu, F., Qu, J., Guan, M. X. (2006) Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families Biochemical and Biophysical Research Communications . 340 (1): 69-75 . |
4 | 16414144 | 2006 | Tang, D. L., Zhou, X., Li, X., Zhao, L., Liu, F. (2006) Variation of mitochondrial gene and the association with type 2 diabetes mellitus in a Chinese population Diabetes Research and Clinical Practice . 73 (1): 77-82 . |
5 | 16947981 | 2006 | Ruiz-Pesini, E., Wallace, D. C. (2006) Evidence for adaptive selection acting on the tRNA and rRNA genes of the human mitochondrial DNA Human Mutation . 27 (11): 1072-1081 . |
6 | 16955413 | 2006 | Young, W. Y., Zhao, L., Qian, Y., Li, R., Chen, J., Yuan, H., Dai, P., Zhai, S., Han, D., Guan, M. X. (2006) Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss American Journal of Medical Genetics. Part A . 140 (20): 2188-2197 . |
7 | 17434142 | 2007 | Tong, Y., Mao, Y., Zhou, X., Yang, L., Zhang, J., Cai, W., Zhao, F., Wang, X., Lu, F., Qu, J., Guan, M. X. (2007) The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy Biochemical and Biophysical Research Communications . 357 (2): 524-530 . |
8 | 18708405 | 2008 | Ye, C., Gao, Y. T., Wen, W., Breyer, J. P., Shu, X. O., Smith, J. R., Zheng, W., Cai, Q. (2008) Association of mitochondrial DNA displacement loop (CA)n dinucleotide repeat polymorphism with breast cancer risk and survival among Chinese women Cancer Epidemiology, Biomarkers and Prevention . 17 (8): 2117-2122 . |
9 | 19376484 | 2009 | Ding, Y., Li, Y., You, J., Yang, L., Chen, B., Lu, J., Guan, M. X. (2009) Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family Journal of Genetics and Genomics (Yi Chuan Xue Bao) . 36 (4): 241-250 . |
10 | 19818876 | 2010 | Lu, J., Qian, Y., Li, Z., Yang, A., Zhu, Y., Li, R., Yang, L., Tang, X., Chen, B., Ding, Y., Li, Y., You, J., Zheng, J., Tao, Z., Zhao, F., Wang, J., Sun, D., Zhao, J., Meng, Y., Guan, M. X. (2010) Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation Mitochondrion . 10 (1): 69-81 . |
11 | 23563965 | 2013 | Levin, L., Zhidkov, I., Gurman, Y., Hawlena, H., Mishmar, D. (2013) Functional recurrent mutations in the human mitochondrial phylogeny: dual roles in evolution and disease Genome Biology and Evolution . 5 (5): 876-890 . |
12 | 29387390 | 2018 | Dai, Y., Wang, C., Nie, Z., Han, J., Chen, T., Zhao, X., Ai, C., Ji, Y., Gao, T., Jiang, P. (2018) Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel Biomedical Reports . 8 (1): 51-58 . |