Index | PMID | Date | Reference |
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1 | 7733935 | 1995 | Nakagawa, Y., Ikegami, H., Yamato, E., Takekawa, K., Fujisawa, T., Hamada, Y., Ueda, H., Uchigata, Y., Miki, T., Kumahara, Y., Ogihara, T. (1995) A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus [published erratum appears in Biochim Biophys Res Commun 209:664-668, 1995] Biochemical and Biophysical Research Communications . 209 (2): 664-668 . |
2 | 8858117 | 1996 | Odawara, M., Sasaki, K., Yamashita, K. (1996) A G-to-A substitution at nucleotide position 3316 in mitochondrial DNA is associated with Japanese non-insulin-dependent diabetes mellitus Biochemical and Biophysical Research Communications . 227 (1): 147-151 . |
3 | 9384601 | 1998 | Sternberg, D., Danan, C., Lombes, A., Laforet, P., Girodon, E., Goossens, M., Amselem, S. (1998) Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders Human Molecular Genetics . 7 (1): 33-42 . |
4 | 10395242 | 1998 | Nakano, S., Fukuda, M., Hotta, F., Ito, T., Ishii, T., Kitazawa, M., Nishizawa, M., Kigoshi, T., Kakinuma, H., Takahashi, H., Uchida, K. (1998) Mitochondrial DNA point mutation at nucleotide pair 3316 in a Japanese family with heterogeneous phenotypes of diabetes Endocrine Journal . 45 (5): 625-630 . |
5 | 10520236 | 1999 | Matsumoto, M., Hayasaka, S., Kadoi, C., Hotta, Y., Fujiki, K., Fujimaki, T., Takeda, M., Ishida, N., Endo, S., Kanai, A. (1999) Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy Ophthalmic Genetics . 20 (3): 153-160 . |
6 | 10636741 | 1999 | Odawara, M., Maki, H., Yamada, N. (1999) Pathogenicity of homoplasmic mitochondrial DNA mutation and nuclear gene involvement Journal of Medical Genetics . 36 (12): 934-935 . |
7 | 10704697 | 2000 | Chen, Y., Liao, W. X., Roy, A. C., Loganath, A., Ng, S. C. (2000) Mitochondrial gene mutations in gestational diabetes mellitus Diabetes Research and Clinical Practice . 48 (1): 29-35 . |
8 | 11238687 | 2001 | Lam, C. W., Yang, T., Tsang, M. W., Pang, C. P. (2001) Homoplasmic 3316G-->A in the ND1 gene of the mitochondrial genome: a pathogenic mutation or a neutral polymorphism? Journal of Medical Genetics . 38 (3): E10 . |
9 | 11961525 | 2002 | Lam, C. W. (2002) Mutation not universally linked with diabetes Nature . 416 (6882): 677 . |
10 | 12436196 | 2002 | Sudoyo, H., Suryadi, H., Lertrit, P., Pramoonjago, P., Lyrawati, D., Marzuki, S. (2002) Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy Journal of Human Genetics . 47 (11): 594-604 . |
11 | 15338331 | 2004 | Mostafaie, N., Rossmanith, W., Hombauer, H., Dechat, T., Raffelsberger, T., Bauer, K., Worofka, B., Kittl, E., Hofmann, J., Hejtman, M., Kirchmeyr, W., Schreiber, W., Weissgram, S., Jungwirth, S., Fischer, P., Bittner, R., Huber, K. (2004) Mitochondrial genotype and risk for Alzheimer's disease: cross-sectional data from the Vienna-Transdanube-Aging "VITA" study Journal of Neural Transmission . 111 (9): 1155-1165 . |
12 | NA | 2005 | Dorraj, G., Houshmand, M., Larijani, B., Majd, A., Hosseini, B., Montazeri, M., Panahi, M. S. (2005) Lack of association of mitochondrial A3243G tRNALeu mutation in Iranian patients with type 2 diabetes Iranian Journal of Biotechnology . 3 (4): 243-248 . |
13 | 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 . |
14 | 15972314 | 2006 | Mitchell, A. L., Elson, J. L., Howell, N., Taylor, R. W., Turnbull, D. M. (2006) Sequence variation in mitochondrial complex I genes: mutation or polymorphism? Journal of Medical Genetics . 43 (2): 175-179 . |
15 | 16409568 | 2006 | Zhang, D., Zhou, Z., Li, L., Weng, J., Huang, G., Jing, P., Zhang, C., Peng, J., Xiu, L. (2006) Islet autoimmunity and genetic mutations in Chinese subjects initially thought to have Type 1B diabetes Diabetic Medicine . 23 (1): 67-71 . |
16 | 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 . |
17 | 16477364 | 2006 | Phasukkijwatana, N., Chuenkongkaew, W. L., Suphavilai, R., Suktitipat, B., Pingsuthiwong, S., Ruangvaravate, N., Atchaneeyasakul, L. O., Warrasak, S., Poonyathalang, A., Sura, T., Lertrit, P. (2006) The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees Journal of Human Genetics . 51 (4): 298-304 . |
18 | 22949535 | 2012 | Liu, C., Yang, Q., Hwang, S. J., Sun, F., Johnson, A. D., Shirihai, O. S., Vasan, R. S., Levy, D., Schwartz, F. (2012) Association of genetic variation in the mitochondrial genome with blood pressure and metabolic traits Hypertension . 60 (4): 949-956 . |
19 | 29987491 | 2018 | O'Keefe, H., Queen, R. A., Meldau, S., Lord, P., Elson, J. L. (2018) Haplogroup context is less important in the penetrance of mitochondrial DNA complex I mutations compared to mt-tRNA mutations Journal of Molecular Evolution . 86 (6): 395-403 . |