-
1
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S., Bankier A.T., Barrell B.G., de Bruijn M.H., Coulson A.R., Drouin J., Eperon I.C., Nierlich D.P., Roe B.A., Sanger F., Schreier P.H., Smith A.J., Staden R., and Young I.G. Sequence and organization of the human mitochondrial genome. Nature 290 (1981) 457-465
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
de Bruijn, M.H.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.12
Staden, R.13
Young, I.G.14
-
2
-
-
28544446736
-
Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection
-
Dunbar S.A. Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection. Clin. Chim. Acta 363 (2006) 71-82
-
(2006)
Clin. Chim. Acta
, vol.363
, pp. 71-82
-
-
Dunbar, S.A.1
-
3
-
-
0035573734
-
Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region
-
Finnila S., Hassinen I.E., and Majamaa K. Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region. Mutat. Res. 458 (2001) 31-39
-
(2001)
Mutat. Res.
, vol.458
, pp. 31-39
-
-
Finnila, S.1
Hassinen, I.E.2
Majamaa, K.3
-
4
-
-
0036299132
-
Mitochondrial ATPase subunit 6 and cytochrome B gene polymorphisms in young obese adults
-
Fuku N., Oshida Y., Takeyasu T., Guo L.J., Kurata M., Yamada Y., Sato Y., and Tanaka M. Mitochondrial ATPase subunit 6 and cytochrome B gene polymorphisms in young obese adults. Biochem. Biophys. Res. Commun. 290 (2002) 1199-1205
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.290
, pp. 1199-1205
-
-
Fuku, N.1
Oshida, Y.2
Takeyasu, T.3
Guo, L.J.4
Kurata, M.5
Yamada, Y.6
Sato, Y.7
Tanaka, M.8
-
5
-
-
85081445605
-
-
Fuku, N., Park, K.S., Yamada, Y., Nishigaki, Y., Cho, Y.M., Matsuo, H., Segawa, T., Watanabe, S., Kato, K., Yokoi, K., Nozawa, Y., Lee, H.K., Tanaka, M. Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians. Am. J. Hum. Genet., in press.
-
-
-
-
6
-
-
0016197604
-
Amino acid difference formula to help explain protein evolution
-
Grantham R. Amino acid difference formula to help explain protein evolution. Science 185 (1974) 862-864
-
(1974)
Science
, vol.185
, pp. 862-864
-
-
Grantham, R.1
-
7
-
-
13344294291
-
Mitochondrial genome polymorphisms associated with type 2 diabetes or obesity
-
Guo L.J., Oshida Y., Fuku N., Takeyasu T., Fujita Y., Kurata M., Sato Y., Ito M., and Tanaka M. Mitochondrial genome polymorphisms associated with type 2 diabetes or obesity. Mitochondrion 5 (2005) 15-33
-
(2005)
Mitochondrion
, vol.5
, pp. 15-33
-
-
Guo, L.J.1
Oshida, Y.2
Fuku, N.3
Takeyasu, T.4
Fujita, Y.5
Kurata, M.6
Sato, Y.7
Ito, M.8
Tanaka, M.9
-
9
-
-
1642399003
-
Genetic risk factors for stroke and carotid atherosclerosis: insights into pathophysiology from candidate gene approaches
-
Humphries S.E., and Morgan L. Genetic risk factors for stroke and carotid atherosclerosis: insights into pathophysiology from candidate gene approaches. Lancet. Neurol. 3 (2004) 227-235
-
(2004)
Lancet. Neurol.
, vol.3
, pp. 227-235
-
-
Humphries, S.E.1
Morgan, L.2
-
10
-
-
0028854722
-
Point mutations of mitochondrial genome in Parkinson's disease
-
Ikebe S., Tanaka M., and Ozawa T. Point mutations of mitochondrial genome in Parkinson's disease. Brain. Res. Mol. Brain. Res. 28 (1995) 281-295
-
(1995)
Brain. Res. Mol. Brain. Res.
, vol.28
, pp. 281-295
-
-
Ikebe, S.1
Tanaka, M.2
Ozawa, T.3
-
11
-
-
27744456947
-
High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population
-
Itoh Y., Mizuki N., Shimada T., Azuma F., Itakura M., Kashiwase K., Kikkawa E., Kulski J.K., Satake M., and Inoko H. High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population. Immunogenetics 57 (2005) 717-729
-
(2005)
Immunogenetics
, vol.57
, pp. 717-729
-
-
Itoh, Y.1
Mizuki, N.2
Shimada, T.3
Azuma, F.4
Itakura, M.5
Kashiwase, K.6
Kikkawa, E.7
Kulski, J.K.8
Satake, M.9
Inoko, H.10
-
12
-
-
3042546349
-
Analysis of 16,922 patients with acute ischemic stroke and transient ischemic attack in Japan. A hospital-based prospective registration study
-
Kimura K., Kazui S., Minematsu K., and Yamaguchi T. Analysis of 16,922 patients with acute ischemic stroke and transient ischemic attack in Japan. A hospital-based prospective registration study. Cerebrovasc. Dis. 18 (2004) 47-56
-
(2004)
Cerebrovasc. Dis.
, vol.18
, pp. 47-56
-
-
Kimura, K.1
Kazui, S.2
Minematsu, K.3
Yamaguchi, T.4
-
13
-
-
33745139842
-
Proportions of stroke subtypes among men and women ≥40 years of age in an urban Japanese city in 1992, 1997, and 2002
-
Kitamura A., Nakagawa Y., Sato M., Iso H., Sato S., Imano H., Kiyama M., Okada T., Okada H., Iida M., and Shimamoto T. Proportions of stroke subtypes among men and women ≥40 years of age in an urban Japanese city in 1992, 1997, and 2002. Stroke 37 (2006) 1374-1378
-
(2006)
Stroke
, vol.37
, pp. 1374-1378
-
-
Kitamura, A.1
Nakagawa, Y.2
Sato, M.3
Iso, H.4
Sato, S.5
Imano, H.6
Kiyama, M.7
Okada, T.8
Okada, H.9
Iida, M.10
Shimamoto, T.11
-
14
-
-
0036045503
-
Effects of estrogen on the vascular wall: vasomotor function and inflammation
-
Koh K.K. Effects of estrogen on the vascular wall: vasomotor function and inflammation. Cardiovasc. Res. 55 (2002) 714-726
-
(2002)
Cardiovasc. Res.
, vol.55
, pp. 714-726
-
-
Koh, K.K.1
-
15
-
-
33745355039
-
Decreasing incidence of lacunar vs. other types of cerebral infarction in a Japanese population
-
Kubo M., Kiyohara Y., Ninomiya T., Tanizaki Y., Yonemoto K., Doi Y., Hata J., Oishi Y., Shikata K., and Iida M. Decreasing incidence of lacunar vs. other types of cerebral infarction in a Japanese population. Neurology 66 (2006) 1539-1544
-
(2006)
Neurology
, vol.66
, pp. 1539-1544
-
-
Kubo, M.1
Kiyohara, Y.2
Ninomiya, T.3
Tanizaki, Y.4
Yonemoto, K.5
Doi, Y.6
Hata, J.7
Oishi, Y.8
Shikata, K.9
Iida, M.10
-
16
-
-
2342559068
-
Association of the mitochondrial DNA 16189 T to C variant with lacunar cerebral infarction: evidence from a hospital-based case-control study
-
Liou C.W., Lin T.K., Huang F.M., Chen T.L., Lee C.F., Chuang Y.C., Tan T.Y., Chang K.C., and Wei Y.H. Association of the mitochondrial DNA 16189 T to C variant with lacunar cerebral infarction: evidence from a hospital-based case-control study. Ann. NY. Acad. Sci. 1011 (2004) 317-324
-
(2004)
Ann. NY. Acad. Sci.
, vol.1011
, pp. 317-324
-
-
Liou, C.W.1
Lin, T.K.2
Huang, F.M.3
Chen, T.L.4
Lee, C.F.5
Chuang, Y.C.6
Tan, T.Y.7
Chang, K.C.8
Wei, Y.H.9
-
17
-
-
0032497128
-
Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
-
Majamaa K., Finnila S., Turkka J., and Hassinen I.E. Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine. Lancet 352 (1998) 455-456
-
(1998)
Lancet
, vol.352
, pp. 455-456
-
-
Majamaa, K.1
Finnila, S.2
Turkka, J.3
Hassinen, I.E.4
-
18
-
-
0035167861
-
Mitochondrial disease and stroke
-
Martinez-Fernandez E., Gil-Peralta A., Garcia-Lozano R., Chinchon I., Aguilera I., Fernandez-Lopez O., Arenas J., Campos Y., and Bautista J. Mitochondrial disease and stroke. Stroke 32 (2001) 2507-2510
-
(2001)
Stroke
, vol.32
, pp. 2507-2510
-
-
Martinez-Fernandez, E.1
Gil-Peralta, A.2
Garcia-Lozano, R.3
Chinchon, I.4
Aguilera, I.5
Fernandez-Lopez, O.6
Arenas, J.7
Campos, Y.8
Bautista, J.9
-
21
-
-
0025412531
-
-
Special report from the National Institute of Neurological Disorders and Stroke. 1990. The Classification of Cerebrovascular Diseases III. Stroke. 21, pp. 637-676.
-
-
-
-
22
-
-
0032539447
-
Mitochondrial genotype associated with longevity
-
Tanaka M., Gong J.S., Zhang J., Yoneda M., and Yagi K. Mitochondrial genotype associated with longevity. Lancet 351 (1998) 185-186
-
(1998)
Lancet
, vol.351
, pp. 185-186
-
-
Tanaka, M.1
Gong, J.S.2
Zhang, J.3
Yoneda, M.4
Yagi, K.5
-
23
-
-
0036420547
-
Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria
-
Tanaka M., Borgeld H.J., Zhang J., Muramatsu S., Gong J.S., Yoneda M., Maruyama W., Naoi M., Ibi T., Sahashi K., Shamoto M., Fuku N., Kurata M., Yamada Y., Nishizawa K., Akao Y., Ohishi N., Miyabayashi S., Umemoto H., Muramatsu T., Furukawa K., Kikuchi A., Nakano I., Ozawa K., and Yagi K. Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria. J. Biomed. Sci. 9 (2002) 534-541
-
(2002)
J. Biomed. Sci.
, vol.9
, pp. 534-541
-
-
Tanaka, M.1
Borgeld, H.J.2
Zhang, J.3
Muramatsu, S.4
Gong, J.S.5
Yoneda, M.6
Maruyama, W.7
Naoi, M.8
Ibi, T.9
Sahashi, K.10
Shamoto, M.11
Fuku, N.12
Kurata, M.13
Yamada, Y.14
Nishizawa, K.15
Akao, Y.16
Ohishi, N.17
Miyabayashi, S.18
Umemoto, H.19
Muramatsu, T.20
Furukawa, K.21
Kikuchi, A.22
Nakano, I.23
Ozawa, K.24
Yagi, K.25
more..
-
24
-
-
6344259029
-
Mitochondrial genome variation in eastern Asia and the peopling of Japan
-
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., and Shimodaira H. Mitochondrial genome variation in eastern Asia and the peopling of Japan. Genome. Res. 14 (2004) 1832-1850
-
(2004)
Genome. Res.
, vol.14
, pp. 1832-1850
-
-
Tanaka, M.1
Cabrera, V.M.2
Gonzalez, A.M.3
Larruga, J.M.4
Takeyasu, T.5
Fuku, N.6
Guo, L.J.7
Hirose, R.8
Fujita, Y.9
Kurata, M.10
Shinoda, K.11
Umetsu, K.12
Yamada, Y.13
Oshida, Y.14
Sato, Y.15
Hattori, N.16
Mizuno, Y.17
Arai, Y.18
Hirose, N.19
Ohta, S.20
Ogawa, O.21
Tanaka, Y.22
Kawamori, R.23
Shamoto-Nagai, M.24
Maruyama, W.25
Shimokata, H.26
Suzuki, R.27
Shimodaira, H.28
more..
-
25
-
-
85081453341
-
-
Tanaka, M., Fuku, N., Nishigaki, Y., Matsuo, H., Segawa, T., Watanabe, S., Kato, K., Yokoi, K., Yamaguchi, S., Nozawa, Y., Yamada, Y. Women with mitochondrial haplogroup N9a are protected against metabolic syndrome. Diabetes, in press.
-
-
-
|