[1] |
Alexe, G., Fuku, N., Bilal, E. et al. Enrichment of longevity phenotype in mtDNA haplogroups D4b2b, D4a, and D4 in the Japanese population Hum. Genet., 121 (2007),pp. 347-356
|
[2] |
Bilal, E., Rabadan, R., Alexe, G. et al. Mitochondrial DNA haplogroup D4a is a marker for extreme longevity in Japan PLoS ONE, 3 (2008),p. e2421
|
[3] |
Chinnery, P.F., Mowbray, C., Patel, S.K. et al. Mitochondrial DNA haplogroups and type 2 diabetes: A study of 897 cases and 1010 controls J. Med. Genet., 44 (2008),p. e80
|
[4] |
Dawson, T.M., Dawson, V.L. Molecular pathway of neurodegeneration in Parkinson's disease Science, 302 (2003),pp. 819-822
|
[5] |
Fuku, N., Park, K.S., Yamada, Y. et al. Mitochondrial haplogroup N9a confers resistance against Type 2 diabetes in Asians Am. J. Hum. Genet., 80 (2007),pp. 407-415
|
[6] |
Feder, J., Blech, I., Ovadia, O. et al. Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications BMC Genomics, 9 (2008),p. 198
|
[7] |
Herrnstadt, C., Elson, J.L., Fahy, E. et al. Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian and European haplogroups Am. J. Hum. Genet., 70 (2002),pp. 1152-1171
|
[8] |
Kim, W., Yoo, T.K., Shin, D.J. et al. Mitochondrial haplogroup analysis reveals no association between the common genetic lineages and prostate cancer in the Korean population PLoS ONE, 3 (2008),p. e2211
|
[9] |
Kosel, S., Egensperger, R., Mehraein, P. et al. No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's disease Biochem. Biophys. Res. Commun., 203 (1994),pp. 745-749
|
[10] |
Kong, Q.P., Yao, Y.G., Sun, C. et al. Phylogeny of East Asian mitochondrial DNA lineages inferred from complete sequences Am. J. Hum. Genet., 73 (2003),pp. 671-676
|
[11] |
Kong, Q.P., Salas, A., Sun, C. et al. Distilling artificial recombinants from large sets of complete mtDNA genomes PLoS ONE, 3 (2008),p. e3016
|
[12] |
Lin, F., Lin, R., Wisniewski, H.M. et al. Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains Biochem. Biophys. Res. Commun., 182 (1992),pp. 238-246
|
[13] |
Lustbader, J.W., Cirilli, M., Lin, C. et al. ABAD directly links Aβ to mitochondrial toxicity in Alzheimer's disease Science, 304 (2004),pp. 448-452
|
[14] |
Mayr-Wohlfart, U., Paulus, C., Rodel, G. Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement Acta Neurol. Scand., 94 (1996),pp. 167-171
|
[15] |
Maruszak, A., Canter, J.A., Styczynska, M. et al. Mitochondrial haplogroup H and Alzheimer's disease—Is there a connection? Neurobiol. Aging (2008)
|
[16] |
Niemi, A.K., Moilanen, J.S., Tanaka, M. et al. A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects Eur. J. Hum. Genet., 13 (2005),pp. 166-170
|
[17] |
Poggio, T., Girosi, F. Networks for approximation and learning Proc. IEEE, 78 (1990),pp. 1481-1497
|
[18] |
Ross, O.A., MaCormack, R., Maxwell, L.D. et al. mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish Exp. Gerontol., 38 (2003),pp. 397-405
|
[19] |
Saxena, R., de Bakker, P.I., Singer, K. et al. Comprehensive association testing of common mitochondrial DNA variation in metabolic disease Am. J. Hum. Genet., 79 (2006),pp. 54-61
|
[20] |
Schoffner, J.M., Brown, M.D., Torroni, A. et al. Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients Genomics, 17 (1993),pp. 171-184
|
[21] |
Schnopp, N.M., Kosel, S., Egensperger, R. et al. Regional heterogeneity of mtDNA hetroplasmy in parkinsonian brain Clin. Neuropathol., 15 (1996),pp. 348-352
|
[22] |
Simon, D.K., Mayeux, R., Marder, K. et al. Mitochondrial DNA mutations in complex I and tRNA genes in Parkinson's disease Neurology, 54 (2000),pp. 703-709
|
[23] |
Tanaka, M., Fuku, N., Takeyasu, T. et al. J. Neurosci. Res., 70 (2002),pp. 347-355
|
[24] |
Tanaka, M., Cabrera, V.M., Gonzalez, A.M. et al. Mitochondrial genome variation in Eastern Asia and the peopling of Japan Genome Res., 14 (2004),pp. 1832-1850
|
[25] |
Takasaki, S., Kawamura, Y., Konagaya, A. Selecting effective siRNA sequences by using radial basis function network and decision tree learning BMC Bioinformatics, 7 (2006),p. S22
|
[26] |
Taylor, R.W., Turnbull, D.M. Mitochondrial DNA mutations in human disease Nat. Rev. Genet., 6 (2005),pp. 389-402
|
[27] |
Vila, M., Przedborski, S. Targeting programmed cell death neurodegenerative diseases Nat. Rev. Neurosci., 4 (2003),pp. 1-11
|
[28] |
Wallace, D.C. Mitochondrial diseases in man and mouse Science, 283 (1999),pp. 1482-1488
|
[29] |
Wu, C.H., McLarty, J.W.
|