Index | PMID | Date | Reference |
---|---|---|---|
1 | 2043137 | 1991 | Ozawa, T., Tanaka, M., Sugiyama, S., Ino, H., Ohno, K., Hattori, K., Ohbayashi, T., Ito, T., Deguchi, H., Kawamura, K., Nakane, Y., Hashiba, K. (1991) Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy Biochemical and Biophysical Research Communications . 177 (1): 518-525 . |
2 | 7723627 | 1995 | Ikebe, S., Tanaka, M., Ozawa, T. (1995) Point mutations of mitochondrial genome in Parkinson's disease Molecular Brain Research . 28 (2): 281-295 . |
3 | 11811990 | 2002 | Fuku, N., Oshida, Y., Takeyasu, T., Guo, L. J., Kurata, M., Yamada, Y., Sato, Y., Tanaka, M. (2002) Mitochondrial ATPase subunit 6 and cytochrome B gene polymorphisms in young obese adults Biochemical and Biophysical Research Communications . 290 (4): 1199-1205 . |
4 | 12870132 | 2003 | Kong, Q. P., Yao, Y. G., Sun, C., Bandelt, H. J., Zhu, C. L., Zhang, Y. P. (2003) Phylogeny of East Asian mitochondrial DNA lineages inferred from complete sequences. [Erratum: Am. J. Hum. Genet., 75:157, 2004] American Journal of Human Genetics . 73 (3): 671-676 . |
5 | 15466285 | 2004 | Tanaka, M., Cabrera, V. M., Gonzalez, A. M., Larruga, J. M., Takeyasu, T., Fuku, N., Guo, L. J., Hirose, R., Fujita, Y., Kurata, M., Shinoda, K., Umetsu, K., Yamada, Y., Oshida, Y., Sato, Y., Hattori, N., Mizuno, Y., Arai, Y., Hirose, N., Ohta, S., Ogawa, O., Tanaka, Y., Kawamori, R., Shamoto-Nagai, M., Maruyama, W., Shimokata, H., Suzuki, R., Shimodaira, H. (2004) Mitochondrial genome variation in eastern Asia and the peopling of Japan Genome Research . 14 (10A): 1832-1850 . |
6 | 15896721 | 2005 | Qian, Y., Zhou, X., Hu, Y., Tong, Y., Li, R., Lu, F., Yang, H., Mo, J. Q., Qu, J., Guan, M. X. (2005) Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy Biochemical and Biophysical Research Communications . 332 (2): 614-621 . |
7 | 16714301 | 2006 | Kong, Q. P., Bandelt, H. J., Sun, C., Yao, Y. G., Salas, A., Achilli, A., Wang, C. Y., Zhong, L., Zhu, C. L., Wu, S. F., Torroni, A., Zhang, Y. P. (2006) Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations Human Molecular Genetics . 15 (13): 2076-2086 . |
8 | 16901986 | 2006 | Fraumene, C., Belle, E. M., Castri, L., Sanna, S., Mancosu, G., Cosso, M., Marras, F., Barbujani, G., Pirastu, M., Angius, A. (2006) High resolution analysis and phylogenetic network construction using complete mtDNA sequences in Sardinian genetic isolates Molecular Biology and Evolution . 23 (11): 2101-2111 . |
9 | 18269758 | 2008 | Abu-Amero, K. K., Larruga, J. M., Cabrera, V. M., Gonzalez, A. M. (2008) Mitochondrial DNA structure in the Arabian Peninsula BMC Evolutionary Biology . 8 (-): 45 . |
10 | 18445251 | 2008 | Feder, J., Blech, I., Ovadia, O., Amar, S., Wainstein, J., Raz, I., Dadon, S., Arking, D. E., Glaser, B., Mishmar, D. (2008) Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications BMC Genomics . 9 (-): 198 . |
11 | 19732751 | 2009 | Zhao, F., Guan, M., Zhou, X., Yuan, M., Liang, M., Liu, Q., Liu, Y., Zhang, Y., Yang, L., Tong, Y., Wei, Q. P., Sun, Y. H., Qu, J., Guan, M. X. (2009) Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation Biochemical and Biophysical Research Communications . 389 (3): 466-472 . |
12 | 20435583 | 2010 | Qu, J., Wang, Y., Tong, Y., Zhou, X., Zhao, F., Yang, L., Zhang, S., Zhang, J., West, C. E., Guan, M. X. (2010) Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families Investigative Ophthalmology and Visual Science . 51 (10): 4906-4912 . |
13 | 20691156 | 2010 | Zhang, J., Zhou, X., Zhou, J., Li, C., Zhao, F., Wang, Y., Meng, Y., Wang, J., Yuan, M., Cai, W., Tong, Y., Sun, Y. H., Yang, L., Qu, J., Guan, M. X. (2010) Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families Biochemical and Biophysical Research Communications . 399 (4): 647-653 . |
14 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
15 | 24467713 | 2014 | Summerer, M., Horst, J., Erhart, G., Weissensteiner, H., Schonherr, S., Pacher, D., Forer, L., Horst, D., Manhart, A., Horst, B., Sanguansermsri, T., Kloss-Brandstatter, A. (2014) Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar BMC Evolutionary Biology . 14 (): 184-192 . |
16 | 24667788 | 2015 | Zhang, J., Zhang, Z. X., Du, P. C., Zhou, W., Wu, S. D., Wang, Q. L., Chen, C., Shi, Q., Chen, C., Gao, C., Tian, C., Dong, X. P. (2015) Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob disease European Journal of Human Genetics . 23 (1): 86-91 . |