Index | PMID | Date | Reference |
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1 | 8033115 | 1994 | Heerdt, B.G., Chen, J., Stewart, L.R., Augenlicht, L.H. (1994) Polymorphisms, but lack of mutations or instability, in the promotor region of the mitochondrial genome in human colonic tumors Cancer Research . 54 (14): 3912-3915 . |
2 | 11133363 | 2001 | Chinnery, P. F., Taylor, G. A., Howell, N., Brown, D. T., Parsons, T. J., Turnbull, D. M. (2001) Point mutations of the mtDNA control region in normal and neurodegenerative human brains American Journal of Human Genetics . 68 (2): 529-532 . |
3 | 11349229 | 2001 | Finnila, S., Lehtonen, M. S., Majamaa, K. (2001) Phylogenetic network for European mtDNA American Journal of Human Genetics . 68 (6): 1475-1484 . |
4 | 12893135 | 2003 | Bini, C., Ceccardi, S., Luiselli, D., Ferri, G., Pelotti, S., Colalongo, C., Falconi, M., Pappalardo, G. (2003) Different informativeness of the three hypervariable mitochondrial DNA regions in the population of Bologna (Italy) Forensic Science International . 135 (1): 48-52 . |
5 | 14593483 | 2004 | Vanecek, T., Vorel, F., Sip, M. (2004) Mitochondrial DNA D-loop hypervariable regions: Czech population data International Journal of Legal Medicine . 118 (1): 14-18 . |
6 | 16050984 | 2005 | Povalko, N., Zakharova, E., Rudenskaia, G., Akita, Y., Hirata, K., Toyojiro, M., Koga, Y. (2005) A new sequence variant in mitochondrial DNA associated with high penetrance of Russian Leber hereditary optic neuropathy Mitochondrion . 5 (3): 194-199 . |
7 | 17429907 | 2007 | Opdal, S. H., Vege, A., Arnestad, M., Musse, M. A., Rognum, T. O. (2007) Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome Acta Paediatr . 96 (2): 211-214 . |
8 | 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 . |
9 | 18842121 | 2008 | Bragoszewski, P., Kupryjanczyk, J., Bartnik, E., Rachinger, A., Ostrowski, J. (2008) Limited clinical relevance of mitochondrial DNA mutation and gene expression analyses in ovarian cancer BMC Cancer . 8 (-): 292 . |
10 | 19151382 | 2009 | Udar, N., Atilano, S. R., Memarzadeh, M., Boyer, D. S., Chwa, M., Lu, S., Maguen, B., Langberg, J., Coskun, P., Wallace, D. C., Nesburn, A. B., Khatibi, N., Hertzog, D., Le, K., Hwang, D., Kenney, M. C. (2009) Mitochondrial DNA haplogroups associated with age-related macular degeneration Investigative Ophthalmology and Visual Science . 50 (6): 2966-2974 . |
11 | 19370763 | 2009 | Dobrowolski, S. F., Gray, J., Miller, T., Sears, M. (2009) Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profiling Human Mutation (Online) . 30 (6): 891-898 . |
12 | 20737604 | 2010 | Pereira, V., Gomes, V., Amorim, A., Gusmao, L., Joao Prata, M. (2010) Genetic characterization of uniparental lineages in populations from Southwest Iberia with past malaria endemicity American Journal of Human Biology . 22 (5): 588-595 . |
13 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
14 | 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 . |
15 | 25703852 | 2016 | Kareem, M. A., Abdulzahra, A. I., Hameed, I. H., Jebor, M. A. (2016) A new polymorphic positions discovered in mitochondrial DNA hypervariable region HVIII from central and north-central of Iraq Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis . 27 (5): 3250-3254 . |
16 | 34034006 | 2021 | Vullo, C. M., Catelli, L., Ibarra Rodriguez, A. A., Papaioannou, A., Merino, J. C. A., Lopez-Parra, A. M., Gaviria, A., Baeza-Richer, C., Romanini, C., Gonzalez-Moya, E., Casals, F., Calafell, F., Berardi, G., Iannacone, G. C., Vicuna Giraldo, G. C., Zorba, G. K., Boschi, I., Olarte, J. V., Ruiz Gomez, J. E., Acierno, J. P., Soto, M. L., Miranda, M. V., Garcia King, M. D., Marrucci, M. A., Porto, M. J., Pinero, M. H., Aler, M., Stephenson Ojea, M. M., Navarrete, S. C., Toscanini, U., Saragoni, V. G., Bozzo, W., Posada Posada, Y. C., Bajunovic, Z., Solla, L. P., Parsons, T. (2021) Second GHEP-ISFG exercise for DVI: "DNA-led" victims' identification in a simulated air crash Forensic Science International: Genetics . 53 (): 102527 . |