메뉴 건너뛰기




Volumn 9, Issue , 2008, Pages

Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients

(21)  Rosa, Alexandra a   Fonseca, Benedita V a   Krug, Tiago a   Manso, Helena a,b   Gouveia, Liliana c   Albergaria, Isabel b   Gaspar, Gisela b   Correia, Manuel d   Viana Baptista, Miguel e   Simões, Rita Moiron f   Pinto, Amélia Nogueira f   Taipa, Ricardo d   Ferreira, Carla g   Fontes, João Ramalho g   Silva, Mário Rui h   Gabriel, João Paulo h   Matos, Ilda i   Lopes, Gabriela d   Ferro, José M c   Vicente, Astrid M a,b   more..


Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 48649083598     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-9-57     Document Type: Article
Times cited : (41)

References (46)
  • 1
    • 7744222619 scopus 로고    scopus 로고
    • Meta-analysis of genetic studies in ischemic stroke: Thirty-two genes involving approximately 18,000 cases and 58,000 controls
    • 10.1001/archneur.61.11.1652 15534175
    • Casas JP Hingorani AD Bautista LE Sharma P Meta-analysis of genetic studies in ischemic stroke: Thirty-two genes involving approximately 18,000 cases and 58,000 controls Arch Neurol 2004, 61:1652-1661 10.1001/ archneur.61.11.1652 15534175
    • (2004) Arch Neurol , vol.61 , pp. 1652-1661
    • Casas, J.P.1    Hingorani, A.D.2    Bautista, L.E.3    Sharma, P.4
  • 4
    • 0032539447 scopus 로고    scopus 로고
    • Mitochondrial genotype associated with longevity
    • 10.1016/S0140-6736(05)78211-8 9449878
    • Tanaka M Gong JS Zhang J Yoneda M Yagi K Mitochondrial genotype associated with longevity Lancet 1998, 351:185-186 10.1016/ S0140-6736(05)78211-8 9449878
    • (1998) Lancet , vol.351 , pp. 185-186
    • Tanaka, M.1    Gong, J.S.2    Zhang, J.3    Yoneda, M.4    Yagi, K.5
  • 5
    • 0031796015 scopus 로고    scopus 로고
    • Mitochondrial genotype associated with French Caucasian centenarians
    • 10.1159/000022041 9813436
    • Ivanova R Lepage V Charron D Schächter F Mitochondrial genotype associated with French Caucasian centenarians Gerontology 1998, 44:349 10.1159/000022041 9813436
    • (1998) Gerontology , vol.44 , pp. 349
    • Ivanova, R.1    Lepage, V.2    Charron, D.3    Schächter, F.4
  • 6
    • 0025666322 scopus 로고
    • A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
    • 10.1038/348651a0 2102678
    • Goto Y Nonaka I Horai S A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies Nature 1990, 348:651-653 10.1038/348651a0 2102678
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 7
    • 0025534162 scopus 로고
    • A point mutation in the mitochondrial tRNA-leu (UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
    • 10.1016/S0006-291X(05)80860-5 2268345
    • Kobayashi Y Momoi MY Tominaga K Momoi T Nihei K Yanagisawa M Kagawa Y Ohta S A point mutation in the mitochondrial tRNA-leu (UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) Biochem Biophys Res Commun 1990, 173:816-822 10.1016/S0006-291X(05)80860-5 2268345
    • (1990) Biochem Biophys Res Commun , vol.173 , pp. 816-822
    • Kobayashi, Y.1    Momoi, M.Y.2    Tominaga, K.3    Momoi, T.4    Nihei, K.5    Yanagisawa, M.6    Kagawa, Y.7    Ohta, S.8
  • 8
    • 0028928397 scopus 로고
    • Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
    • 1206556 7635294
    • Howell N Kubacka I Halvorson S Howell B McCullough DA Mackey D Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees Genetics 1995, 140:285-302 1206556 7635294
    • (1995) Genetics , vol.140 , pp. 285-302
    • Howell, N.1    Kubacka, I.2    Halvorson, S.3    Howell, B.4    McCullough, D.A.5    Mackey, D.6
  • 9
    • 16944363113 scopus 로고    scopus 로고
    • Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
    • 1712418 9150158
    • Torroni A Petrozzi M D'Urbano L Sellitto D Zeviani M Carrara F Carducci C Leuzzi V Carelli V Barboni P De Negri A Scozzari R Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484 Am J Hum Genet 1997, 60:1107-1121 1712418 9150158
    • (1997) Am J Hum Genet , vol.60 , pp. 1107-1121
    • Torroni, A.1    Petrozzi, M.2    D'Urbano, L.3    Sellitto, D.4    Zeviani, M.5    Carrara, F.6    Carducci, C.7    Leuzzi, V.8    Carelli, V.9    Barboni, P.10    De Negri, A.11    Scozzari, R.12
  • 14
    • 0141920798 scopus 로고    scopus 로고
    • Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population
    • 10.1007/s00439-003-0983-8 12905068
    • Okura T Koda M Ando F Niino N Tanaka M Shimokata H Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population Hum Genet 2003, 113:432-436 10.1007/ s00439-003-0983-8 12905068
    • (2003) Hum Genet , vol.113 , pp. 432-436
    • Okura, T.1    Koda, M.2    Ando, F.3    Niino, N.4    Tanaka, M.5    Shimokata, H.6
  • 15
    • 0032497128 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
    • 10.1016/S0140-6736(05)79190-X 9708761
    • Majamaa K Finnilä S Turkka J Hassinen IE Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine Lancet 1998, 352:455-456 10.1016/S0140-6736(05)79190-X 9708761
    • (1998) Lancet , vol.352 , pp. 455-456
    • Majamaa, K.1    Finnilä, S.2    Turkka, J.3    Hassinen, I.E.4
  • 16
    • 0035573734 scopus 로고    scopus 로고
    • Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region
    • 11406419
    • Finnila S Hassinen IE 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 2001, 458:31-39 11406419
    • (2001) Mutat Res , vol.458 , pp. 31-39
    • Finnila, S.1    Hassinen, I.E.2    Majamaa, K.3
  • 18
    • 36248971209 scopus 로고    scopus 로고
    • The putative role of mitochondrial dysfunction in hypertension
    • 10.1080/10641960701613852 17994352
    • Puddu P Puddu GM Cravero E De Pascalis S Muscari A The putative role of mitochondrial dysfunction in hypertension Clin Exp Hypertens 2007, 29:427-434 10.1080/10641960701613852 17994352
    • (2007) Clin Exp Hypertens , vol.29 , pp. 427-434
    • Puddu, P.1    Puddu, G.M.2    Cravero, E.3    De Pascalis, S.4    Muscari, A.5
  • 22
    • 0027514354 scopus 로고
    • Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment
    • 7678184
    • Adams HP Jr Bendixen BH Kappelle LJ Biller J Love BB Gordon DL Marsh EE 3rd Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment Stroke 1993, 24:35-41 7678184
    • (1993) Stroke , vol.24 , pp. 35-41
    • Adams Jr., H.P.1    Bendixen, B.H.2    Kappelle, L.J.3    Biller, J.4    Love, B.B.5    Gordon, D.L.6    Marsh III, E.E.7
  • 23
    • 0034472023 scopus 로고    scopus 로고
    • Diversity of mtDNA lineages in Portugal: Not a genetic edge of European variation
    • 10.1046/j.1469-1809.2000.6460491.x 11281213
    • Pereira L Prata MJ Amorim A Diversity of mtDNA lineages in Portugal: Not a genetic edge of European variation Ann Hum Genet 2000, 64:491-506 10.1046/j.1469-1809.2000.6460491.x 11281213
    • (2000) Ann Hum Genet , vol.64 , pp. 491-506
    • Pereira, L.1    Prata, M.J.2    Amorim, A.3
  • 26
    • 0031671129 scopus 로고    scopus 로고
    • Phylogeography of mitochondrial DNA in western Europe
    • 10.1046/j.1469-1809.1998.6230241.x 9803269
    • Richards MB Macaulay VA Bandelt HJ Sykes BC Phylogeography of mitochondrial DNA in western Europe Ann Hum Genet 1998, 62:241-260 10.1046/j.1469-1809.1998.6230241.x 9803269
    • (1998) Ann Hum Genet , vol.62 , pp. 241-260
    • Richards, M.B.1    Macaulay, V.A.2    Bandelt, H.J.3    Sykes, B.C.4
  • 30
    • 33644877057 scopus 로고    scopus 로고
    • Genotype and haplotype association study of the STRK1 region on 5q12 among Japanese: A case-control study
    • 10.1161/01.STR.0000194961.17292.33 16322495
    • Nakayama T Asai S Sato N Soma M Genotype and haplotype association study of the STRK1 region on 5q12 among Japanese: A case-control study Stroke 2006, 37:69-76 10.1161/01.STR.0000194961.17292.33 16322495
    • (2006) Stroke , vol.37 , pp. 69-76
    • Nakayama, T.1    Asai, S.2    Sato, N.3    Soma, M.4
  • 32
    • 33646929523 scopus 로고    scopus 로고
    • Harvesting the fruit of the human mtDNA tree
    • 10.1016/j.tig.2006.04.001 16678300
    • Torroni A Achilli A Macaulay V Richards M Bandelt HJ Harvesting the fruit of the human mtDNA tree Trends Genet 2006, 22:339-345 10.1016/ j.tig.2006.04.001 16678300
    • (2006) Trends Genet , vol.22 , pp. 339-345
    • Torroni, A.1    Achilli, A.2    Macaulay, V.3    Richards, M.4    Bandelt, H.J.5
  • 33
    • 0037477428 scopus 로고    scopus 로고
    • Sex differences in first-ever acute stroke
    • 10.1161/01.STR.0000078562.82918.F6 12805490
    • Roquer J Campello AR Gomis M Sex differences in first-ever acute stroke Stroke 2003, 34:1581-1585 10.1161/01.STR.0000078562.82918.F6 12805490
    • (2003) Stroke , vol.34 , pp. 1581-1585
    • Roquer, J.1    Campello, A.R.2    Gomis, M.3
  • 34
    • 0034676760 scopus 로고    scopus 로고
    • Increased risk of stroke in patients with the A12308G polymorphism in mitochondria
    • 10.1016/S0140-6736(00)03408-5 11145497
    • Pulkes T Sweeney MG Hanna MG Increased risk of stroke in patients with the A12308G polymorphism in mitochondria Lancet 2000, 356:2068-2069 10.1016/S0140-6736(00)03408-5 11145497
    • (2000) Lancet , vol.356 , pp. 2068-2069
    • Pulkes, T.1    Sweeney, M.G.2    Hanna, M.G.3
  • 35
    • 0037098607 scopus 로고    scopus 로고
    • Cerebrovascular disorders and genetic polymorphisms: Mitochondrial DNA5178C is predominant in cerebrovascular disorders
    • 10.1016/S0022-510X(02)00055-2 12039661
    • Ohkubo R Nakagawa M Ikeda K Kodama T Arimura K Akiba S Saito M Ookatsu Y Atsuchi Y Yamano Y Osame M Cerebrovascular disorders and genetic polymorphisms: Mitochondrial DNA5178C is predominant in cerebrovascular disorders J Neurol Sci 2002, 198:31-35 10.1016/S0022-510X(02)00055-2 12039661
    • (2002) J Neurol Sci , vol.198 , pp. 31-35
    • Ohkubo, R.1    Nakagawa, M.2    Ikeda, K.3    Kodama, T.4    Arimura, K.5    Akiba, S.6    Saito, M.7    Ookatsu, Y.8    Atsuchi, Y.9    Yamano, Y.10    Osame, M.11
  • 36
    • 33947311219 scopus 로고    scopus 로고
    • HmtDB, a Human Mitochondrial Genomic Resource Based on Variability Studies Supporting Population Genetics and Biomedical Research
    • 1866381 16351753 10.1186/1471-2105-6-S4-S4
    • Attimonelli M Accetturo M Santamaria M Lascaro D Scioscia G Pappada G Russo L Zanchetta L Tommaseo-Ponzetta M HmtDB, a Human Mitochondrial Genomic Resource Based on Variability Studies Supporting Population Genetics and Biomedical Research BMC Bioinformatics 2005, 6(Suppl 4):S4 1866381 16351753 10.1186/1471-2105-6-S4-S4
    • (2005) BMC Bioinformatics , vol.6 , Issue.SUPPL. 4
    • Attimonelli, M.1    Accetturo, M.2    Santamaria, M.3    Lascaro, D.4    Scioscia, G.5    Pappada, G.6    Russo, L.7    Zanchetta, L.8    Tommaseo-Ponzetta, M.9
  • 38
    • 2342559068 scopus 로고    scopus 로고
    • Association of the mitochondrial DNA 16189 T to C variant with lacunar cerebral infarction: Evidence from a hospital-based case-control study
    • 10.1196/annals.1293.031 15126308
    • Liou CW Lin TK Huang FM Chen TL Lee CF Chuang YC Tan TY Chang KC Wei YH Association of the mitochondrial DNA 16189 T to C variant with lacunar cerebral infarction: Evidence from a hospital-based case-control study Ann N Y Acad Sci 2004, 1011:317-324 10.1196/annals.1293.031 15126308
    • (2004) Ann N Y 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
  • 39
    • 0842307218 scopus 로고    scopus 로고
    • Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlers
    • 10.1007/s00439-003-1024-3 14513360
    • Brehm A Pereira L Kivisild T Amorim A Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlers Hum Genet 2003, 114:77-86 10.1007/s00439-003-1024-3 14513360
    • (2003) Hum Genet , vol.114 , pp. 77-86
    • Brehm, A.1    Pereira, L.2    Kivisild, T.3    Amorim, A.4
  • 40
    • 2942524128 scopus 로고    scopus 로고
    • Major genomic mitochondrial lineages delineate early human expansions
    • 55343 11553319 10.1186/1471-2156-2-13
    • Maca-Meyer N González AM Larruga JM Flores C Cabrera VM Major genomic mitochondrial lineages delineate early human expansions BMC Genet 2001, 2:13 55343 11553319 10.1186/1471-2156-2-13
    • (2001) BMC Genet , vol.2 , pp. 13
    • Maca-Meyer, N.1    González, A.M.2    Larruga, J.M.3    Flores, C.4    Cabrera, V.M.5
  • 41
    • 33645474357 scopus 로고    scopus 로고
    • The power to detect disease associations with mitochondrial DNA haplogroups
    • 1424681 16532401 10.1086/502682
    • Samuels DC Carothers AD Horton R Chinnery PF The power to detect disease associations with mitochondrial DNA haplogroups Am J Hum Genet 2006, 78:713-720 1424681 16532401 10.1086/502682
    • (2006) Am J Hum Genet , vol.78 , pp. 713-720
    • Samuels, D.C.1    Carothers, A.D.2    Horton, R.3    Chinnery, P.F.4
  • 42
    • 0027017232 scopus 로고
    • Mitochondrial DNA deletions in human brain: Regional variability and increase with advanced age
    • 10.1038/ng1292-324 1303288
    • Corral-Debrinski M Horton T Lott MT Shoffner JM Beal MF Wallace DC Mitochondrial DNA deletions in human brain: Regional variability and increase with advanced age Nat Genet 1992, 2:324-329 10.1038/ng1292-324 1303288
    • (1992) Nat Genet , vol.2 , pp. 324-329
    • Corral-Debrinski, M.1    Horton, T.2    Lott, M.T.3    Shoffner, J.M.4    Beal, M.F.5    Wallace, D.C.6
  • 43
    • 33646807843 scopus 로고    scopus 로고
    • Tissue-specific deletion patterns of the mitochondrial genome with advancing age
    • 10.1016/j.exger.2006.03.010 16624514
    • Meissner C Bruse P Oehmichen M Tissue-specific deletion patterns of the mitochondrial genome with advancing age Exp Gerontol 2006, 41:518-524 10.1016/j.exger.2006.03.010 16624514
    • (2006) Exp Gerontol , vol.41 , pp. 518-524
    • Meissner, C.1    Bruse, P.2    Oehmichen, M.3
  • 44
    • 0019448863 scopus 로고
    • Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance
    • 10.1038/290607a0 7219548
    • Kearsey SE Craig IW Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance Nature 1981, 290:607-608 10.1038/290607a0 7219548
    • (1981) Nature , vol.290 , pp. 607-608
    • Kearsey, S.E.1    Craig, I.W.2
  • 45
    • 0024448458 scopus 로고
    • Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation
    • 10.1126/science.2814477 2814477
    • King MP Attardi G Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation Science 1989, 246:500-503 10.1126/ science.2814477 2814477
    • (1989) Science , vol.246 , pp. 500-503
    • King, M.P.1    Attardi, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.