메뉴 건너뛰기




Volumn 72, Issue 1, 2006, Pages 37-47

Mitochondrial lineages distribution in the Spanish population: Anticipating association studies

Author keywords

Haplogroups; Human; Mitochondrial DNA; Oxidative phosphorylation; Variability

Indexed keywords

ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; MITOCHONDRION; POPULATION; SPAIN;

EID: 33746032572     PISSN: None     EISSN: 1697428X     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (10)

References (35)
  • 1
    • 0031034482 scopus 로고    scopus 로고
    • Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage
    • BROWN, M. D.; SUN, F. and WALLACE, D. C. (1997): Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet 60, 381-7.
    • (1997) Am J Hum Genet , vol.60 , pp. 381-387
    • Brown, M.D.1    Sun, F.2    Wallace, D.C.3
  • 2
    • 0030813676 scopus 로고    scopus 로고
    • Population genetics and disease susceptibility: Characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease
    • HOFMANN, S.; JAKSCH, M.; BEZOLD, R.; MERTENS, S.; AHOLT, S.; PAPROTTA, A. and GERBITZ, K. D. (1997): Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease. Hum Mol Genet 6, 1835-46.
    • (1997) Hum Mol Genet , vol.6 , pp. 1835-1846
    • Hofmann, S.1    Jaksch, M.2    Bezold, R.3    Mertens, S.4    Aholt, S.5    Paprotta, A.6    Gerbitz, K.D.7
  • 4
    • 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
    • TORRONI, A. et al. (1997): 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 60, 1107-21.
    • (1997) Am J Hum Genet , vol.60 , pp. 1107-1121
    • Torroni, A.1
  • 5
    • 0033842465 scopus 로고    scopus 로고
    • Human mtDNA haplogroups associated with high or reduced spermatozoa motility
    • RUIZ-PESINI, E. et al. (2000): Human mtDNA haplogroups associated with high or reduced spermatozoa motility. Am J Hum Genet 67, 682-96.
    • (2000) Am J Hum Genet , vol.67 , pp. 682-696
    • Ruiz-Pesini, E.1
  • 7
    • 0031796015 scopus 로고    scopus 로고
    • Mitochondrial genotype associated with French Caucasian centenarians
    • IVANOVA, R.; LEPAGE, V.; CHARRON, D. and SCHACHTER, F. (1998): Mitochondrial genotype associated with French Caucasian centenarians. Gerontology 44, 349.
    • (1998) Gerontology , vol.44 , pp. 349
    • Ivanova, R.1    Lepage, V.2    Charron, D.3    Schachter, F.4
  • 8
    • 0032539447 scopus 로고    scopus 로고
    • Mitochondrial genotype associated with longevity
    • TANAKA, M.; GONG, J. S.; ZHANG, J.; YONEDA, M. and YAGI, K. (1998): Mitochondrial genotype associated with longevity. Lancet 351, 185-6.
    • (1998) Lancet , vol.351 , pp. 185-186
    • Tanaka, M.1    Gong, J.S.2    Zhang, J.3    Yoneda, M.4    Yagi, K.5
  • 9
    • 0032851615 scopus 로고    scopus 로고
    • Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans
    • DE BENEDICTIS, G. et al. (1999): Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans. Faseb J 13, 1532-6.
    • (1999) Faseb J , vol.13 , pp. 1532-1536
    • De Benedictis, G.1
  • 10
    • 0037209210 scopus 로고    scopus 로고
    • Mitochondrial DNA polymorphisms associated with longevity in a Finnish population
    • NIEMI, A. K.; HERVONEN, A.; HURME, M.; KARHUNEN, P. J.; JYLHA, M. and MAJAMAA, K. (2003): Mitochondrial DNA polymorphisms associated with longevity in a Finnish population. Hum Genet 112, 29-33.
    • (2003) Hum Genet , vol.112 , pp. 29-33
    • Niemi, A.K.1    Hervonen, A.2    Hurme, M.3    Karhunen, P.J.4    Jylha, M.5    Majamaa, K.6
  • 11
    • 0037385480 scopus 로고    scopus 로고
    • Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
    • VAN DER WALT, J. M. et al. (2003): Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. Am J Hum Genet 72, 804-11.
    • (2003) Am J Hum Genet , vol.72 , pp. 804-811
    • Van Der Walt, J.M.1
  • 12
    • 20544461885 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians
    • GHEZZI, D. et al. (2005): Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians. Eur J Hum Genet 13, 748-52.
    • (2005) Eur J Hum Genet , vol.13 , pp. 748-752
    • Ghezzi, D.1
  • 13
    • 20144389920 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD
    • PYLE, A. et al. (2005): Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD. Ann Neurol 57, 564-7.
    • (2005) Ann Neurol , vol.57 , pp. 564-567
    • Pyle, A.1
  • 14
    • 0033516529 scopus 로고    scopus 로고
    • Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population
    • CHAGNON, P.; GEE, M.; FILION, M.; ROBITAILLE, Y.; BELOUCHI, M. and GAUVREAU, D. (1999): Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population. Am J Med Genet 85, 20-30.
    • (1999) Am J Med Genet , vol.85 , pp. 20-30
    • Chagnon, P.1    Gee, M.2    Filion, M.3    Robitaille, Y.4    Belouchi, M.5    Gauvreau, D.6
  • 15
    • 33646156243 scopus 로고    scopus 로고
    • Maternal lineages and Alzheimer disease risk in the Old Order Amish
    • VAN DER WALT, J. M. et al. (2005): Maternal lineages and Alzheimer disease risk in the Old Order Amish. Hum Genet 118, 115-22.
    • (2005) Hum Genet , vol.118 , pp. 115-122
    • Van Der Walt, J.M.1
  • 16
    • 0037422550 scopus 로고    scopus 로고
    • Natural selection shaped regional mtDNA variation in humans
    • MISHMAR, D. et al. (2003): Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci USA 100, 171-6.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 171-176
    • Mishmar, D.1
  • 17
    • 3242676865 scopus 로고    scopus 로고
    • DNA variation, climatic adaptation, degenerative diseases, and longevity
    • WALLACE, D. C.; RUIZ-PESINI, E. and MISHMAR, D. (2003): mtDNA variation, climatic adaptation, degenerative diseases, and longevity. Cold Spring Harb Symp Quant Biol 68, 479-86.
    • (2003) Cold Spring Harb Symp Quant Biol , vol.68 , pp. 479-486
    • Wallace, D.C.1    Ruiz-Pesini, E.2    Mishmar, D.3
  • 18
    • 0347356538 scopus 로고    scopus 로고
    • Effects of purifying and adaptive selection on regional variation in human mtDNA
    • RUIZ-PESINI, E.; MISHMAR, D.; BRANDON, M.; PROCACCIO, V. and WALLACE, D. C. (2004): Effects of purifying and adaptive selection on regional variation in human mtDNA. Science 303, 223-6.
    • (2004) Science , vol.303 , pp. 223-226
    • Ruiz-Pesini, E.1    Mishmar, D.2    Brandon, M.3    Procaccio, V.4    Wallace, D.C.5
  • 19
    • 0032833421 scopus 로고    scopus 로고
    • Mitochondria! DNA variation in human evolution and disease
    • WALLACE, D. C.; BROWN, M. D. and LOTT, M. T. (1999): Mitochondria! DNA variation in human evolution and disease. Gene 238, 211-30.
    • (1999) Gene , vol.238 , pp. 211-230
    • Wallace, D.C.1    Brown, M.D.2    Lott, M.T.3
  • 20
    • 0030468182 scopus 로고    scopus 로고
    • Classification of European mtDNAs from an analysis of three European populations
    • TORRONI, A. et al. (1996): Classification of European mtDNAs from an analysis of three European populations. Genetics 144, 1835-50.
    • (1996) Genetics , vol.144 , pp. 1835-1850
    • Torroni, A.1
  • 21
    • 6344223665 scopus 로고    scopus 로고
    • The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool
    • ACHILLI, A. et al. (2004): The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool. Am J Hum Genet 75, 910-8.
    • (2004) Am J Hum Genet , vol.75 , pp. 910-918
    • Achilli, A.1
  • 22
    • 6344241453 scopus 로고    scopus 로고
    • Disuniting uniformity: A pied cladistic canvas of mtDNA haplogroup H in Eurasia
    • LOOGVALI, E. L. et al. (2004): Disuniting uniformity: a pied cladistic canvas of mtDNA haplogroup H in Eurasia. Mol Biol Evol 21, 2012-21.
    • (2004) Mol Biol e , vol.21 , pp. 2012-2021
    • Loogvali, E.L.1
  • 23
    • 19944431813 scopus 로고    scopus 로고
    • High-resolution mtDNA evidence for the late-glacial resettlement of Europe from an Iberian refugium
    • PEREIRA, L. et al. (2005): High-resolution mtDNA evidence for the late-glacial resettlement of Europe from an Iberian refugium. Genome Res 15, 19-24.
    • (2005) Genome Res , vol.15 , pp. 19-24
    • Pereira, L.1
  • 24
    • 33645344999 scopus 로고    scopus 로고
    • Haplogroup effects and recombination of mitochondrial DNA: Novel clues from the analysis of leber hereditary optic neuropathy pedigrees
    • CARELLI, V. et al. (2006): Haplogroup effects and recombination of mitochondrial DNA: Novel clues from the analysis of leber hereditary optic neuropathy pedigrees. Am J Hum Genet 78, 564-74.
    • (2006) Am J Hum Genet , vol.78 , pp. 564-574
    • Carelli, V.1
  • 27
    • 0033764821 scopus 로고    scopus 로고
    • Tracing European founder lineages in the Near Eastern mtDNA pool
    • RICHARDS, M. et al. (2000): Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet 67, 1251-76.
    • (2000) Am J Hum Genet , vol.67 , pp. 1251-1276
    • Richards, M.1
  • 28
    • 0033361927 scopus 로고    scopus 로고
    • The A1555G mutation in the 12S rRNA gene of human mtDNA: Recurrent origins and founder events in families affected by sensorineural deafness
    • TORRONI, A. et al. (1999): The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness. Am J Hum Genet 65, 1349-58.
    • (1999) Am J Hum Genet , vol.65 , pp. 1349-1358
    • Torroni, A.1
  • 29
    • 0032497128 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
    • MAJAMAA, K.; FINNILA, S.; TURKKA, J. and HASSINEN, I. E. (1998): Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine. Lancet 352, 455-6.
    • (1998) Lancet , vol.352 , pp. 455-456
    • Majamaa, K.1    Finnila, S.2    Turkka, J.3    Hassinen, I.E.4
  • 30
    • 0034676760 scopus 로고    scopus 로고
    • Increased risk of stroke in patients with the A12308G polymorphism in mitochondria
    • PULKES, T.; SWEENEY, M. G. and HANNA, M. G. (2000): Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. Lancet 356, 2068-9.
    • (2000) Lancet , vol.356 , pp. 2068-2069
    • Pulkes, T.1    Sweeney, M.G.2    Hanna, M.G.3
  • 31
    • 0242609815 scopus 로고    scopus 로고
    • Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
    • CRIMI, M.; DEL Bo, R.; GALBIATI, S.; SCIACCO, M.; BORDONI, A.; BRESOLIN, N. and COMI, G. P. (2003): Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion. Eur J Hum Genet 11, 896-8.
    • (2003) Eur J Hum Genet , vol.11 , pp. 896-898
    • Crimi, M.1    Del Bo, R.2    Galbiati, S.3    Sciacco, M.4    Bordoni, A.5    Bresolin, N.6    Comi, G.P.7
  • 32
    • 0345701481 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation
    • TORRONI, A. et al. (2003): Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation. Am J Hum Genet 72, 1005-12.
    • (2003) Am J Hum Genet , vol.72 , pp. 1005-1012
    • Torroni, A.1
  • 33
    • 0026236503 scopus 로고
    • Call for a worldwide survey of human genetic diversity: A vanishing opportunity for the Human Genome Project
    • CAVALLI-SFORZA, L. L.; WILSON, A. C.; CANTOR, C. R.; COOK-DEEGAN, R. M. and KING, M. C. (1991): Call for a worldwide survey of human genetic diversity: a vanishing opportunity for the Human Genome Project. Genomics 11, 490-1.
    • (1991) Genomics , vol.11 , pp. 490-491
    • Cavalli-Sforza, L.L.1    Wilson, A.C.2    Cantor, C.R.3    Cook-Deegan, R.M.4    King, M.C.5
  • 34
    • 1542360077 scopus 로고    scopus 로고
    • Joining the pillars of Hercules: MtDNA sequences show multidirectional gene flow in the western Mediterranean
    • PLAZA, S.; CALAFELL, F.; HELAL, A.; BOUZERNA, N.; LEFRANC, G.; BERTRANPETIT, J. and COMAS, D. (2003): Joining the pillars of Hercules: mtDNA sequences show multidirectional gene flow in the western Mediterranean. Ann Hum Genet 67, 312-28.
    • (2003) Ann Hum Genet , vol.67 , pp. 312-328
    • Plaza, S.1    Calafell, F.2    Helal, A.3    Bouzerna, N.4    Lefranc, G.5    Bertranpetit, J.6    Comas, D.7
  • 35
    • 24044555258 scopus 로고    scopus 로고
    • Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population
    • HUERTA, C. et al. (2005): Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population. J Neurol Sci 236, 49-54.
    • (2005) J Neurol Sci , vol.236 , pp. 49-54
    • Huerta, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.