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Volumn 1, Issue 5, 1996, Pages 288-295

The evolutionary relationship among Caucasian MS patients and controls

Author keywords

Genetic relationship; Mitochondrial DNA

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0030112473     PISSN: 13524585     EISSN: None     Source Type: Journal    
DOI: 10.1177/135245859600100505     Document Type: Article
Times cited : (3)

References (47)
  • 1
    • 0028351997 scopus 로고
    • Genetics and multiple sclerosis: An overview
    • Ebers GC. (1994) Genetics and multiple sclerosis: An overview. Ann Neurol 36: S12-S14.
    • (1994) Ann Neurol , vol.36
    • Ebers, G.C.1
  • 2
    • 0027164123 scopus 로고
    • Familial recurrence risk and inheritance of multiple sclerosis
    • Sadovnick AD. (1993) Familial recurrence risk and inheritance of multiple sclerosis. Curr Opin Neurol Neurosurg 6: 189-194.
    • (1993) Curr Opin Neurol Neurosurg , vol.6 , pp. 189-194
    • Sadovnick, A.D.1
  • 3
    • 0022868088 scopus 로고
    • A population-based study of multiple sclerosis in twins
    • Ebers GC et al. (1986) A population-based study of multiple sclerosis in twins. New Eng J Med 315: 1638-1642.
    • (1986) New Eng J Med , vol.315 , pp. 1638-1642
    • Ebers, G.C.1
  • 4
    • 0020477385 scopus 로고
    • Concordance in twins and recurrence in sibships in multiple sclerosis
    • Heltberg A, Holm NV. (1982) Concordance in twins and recurrence in sibships in multiple sclerosis. Lancet 1: 1068.
    • (1982) Lancet , vol.1 , pp. 1068
    • Heltberg, A.1    Holm, N.V.2
  • 5
    • 0019499988 scopus 로고
    • The familial nature of multiple sclerosis: Empiric recurrence risks for first, second-, and third-degree relatives of patients
    • Sadovnick AD, Macleod PMJ. (1981) The familial nature of multiple sclerosis: empiric recurrence risks for first, second-, and third-degree relatives of patients. Neurology, 31: 1039-1041.
    • (1981) Neurology , vol.31 , pp. 1039-1041
    • Sadovnick, A.D.1    Macleod, P.M.J.2
  • 6
    • 0023897491 scopus 로고
    • Multiple sclerosis: Updated risk for relatives
    • Sadovnick AD et al. (1988) Multiple sclerosis: Updated risk for relatives. Am J Med Gen 29: 533-541.
    • (1988) Am J Med Gen , vol.29 , pp. 533-541
    • Sadovnick, A.D.1
  • 7
    • 0001782589 scopus 로고
    • HLA-Dw2 in multiple sclerosis: A world-wide association and a close segregation with disease in multiplex families
    • Hillert J et al. (1993) HLA-Dw2 in multiple sclerosis: a world-wide association and a close segregation with disease in multiplex families. Hum Immunol 36: 50.
    • (1993) Hum Immunol , vol.36 , pp. 50
    • Hillert, J.1
  • 8
    • 0025292979 scopus 로고
    • Association between the lack of HLA DQw6 and the low incidence of multiple sclerosis in Hungarian Gypsies
    • Takacs K et al. (1990) Association between the lack of HLA DQw6 and the low incidence of multiple sclerosis in Hungarian Gypsies. Immunogenetics 31: 383-385.
    • (1990) Immunogenetics , vol.31 , pp. 383-385
    • Takacs, K.1
  • 9
    • 0027235992 scopus 로고
    • Susceptibility for multiple sclerosis is determined, in part, by inheritance of a 175 kb region of the TCR Vβ chain locus and HLA class II genes
    • Beall SS et al. (1993) Susceptibility for multiple sclerosis is determined, in part, by inheritance of a 175 kb region of the TCR Vβ chain locus and HLA class II genes. J Neuroimmunol 45: 53-60.
    • (1993) J Neuroimmunol , vol.45 , pp. 53-60
    • Beall, S.S.1
  • 10
    • 0025895224 scopus 로고
    • Allele frequencies of the third component of complement (C3) in MS patients
    • Bulman DE et al. (1991) Allele frequencies of the third component of complement (C3) in MS patients. J Neurol Neurosurg Psychiatry 54: 554-555.
    • (1991) J Neurol Neurosurg Psychiatry , vol.54 , pp. 554-555
    • Bulman, D.E.1
  • 11
    • 0019424530 scopus 로고
    • Immunoglobulin G heavy chain (Gm) allotypes in multiple sclerosis
    • Pandey JP et al. (1981) Immunoglobulin G heavy chain (Gm) allotypes in multiple sclerosis. J Clin Invest 67: 1797-1800.
    • (1981) J Clin Invest , vol.67 , pp. 1797-1800
    • Pandey, J.P.1
  • 12
    • 0025317768 scopus 로고
    • DNA length polymorphism 5′ to the myelin basic protein gene is associated with multiple sclerosis
    • Boylan KB et al. (1990) DNA length polymorphism 5′ to the myelin basic protein gene is associated with multiple sclerosis. Ann Neurol 27: 291-297.
    • (1990) Ann Neurol , vol.27 , pp. 291-297
    • Boylan, K.B.1
  • 13
    • 0001174007 scopus 로고
    • Leber's optic atrophy and its relation to the heredo-familial ataxias
    • Ferguson FR, Critchley M. (1928) Leber's optic atrophy and its relation to the heredo-familial ataxias. J Neurol Psychol 9: 120-132.
    • (1928) J Neurol Psychol , vol.9 , pp. 120-132
    • Ferguson, F.R.1    Critchley, M.2
  • 14
    • 0000514888 scopus 로고
    • Leber's disease with symptoms resembling disseminated sclerosis
    • Lees F et al. (1964) Leber's disease with symptoms resembling disseminated sclerosis. J Neurol Neurosurg Psychiatry 27: 415-421.
    • (1964) J Neurol Neurosurg Psychiatry , vol.27 , pp. 415-421
    • Lees, F.1
  • 15
    • 0002699021 scopus 로고
    • A sex-linked heredo-degenerative neurological disorder, associated with Leber's optic atrophy. Part I. Clinical studies
    • Bruyn GW et al. (1964) A sex-linked heredo-degenerative neurological disorder, associated with Leber's optic atrophy. Part I. Clinical studies. J Neurol Sci 1: 59-80.
    • (1964) J Neurol Sci , vol.1 , pp. 59-80
    • Bruyn, G.W.1
  • 16
    • 0026782507 scopus 로고
    • Occurrence of multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
    • Harding AE et al. (1992) Occurrence of multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain 115: 979-989.
    • (1992) Brain , vol.115 , pp. 979-989
    • Harding, A.E.1
  • 17
    • 0027731794 scopus 로고
    • Association of the 11778 mitochondrial DNA mutation and demyelinating disease
    • Flanigan KM, Johns DR. (1993) Association of the 11778 mitochondrial DNA mutation and demyelinating disease. Neurology 43: 2720-2722.
    • (1993) Neurology , vol.43 , pp. 2720-2722
    • Flanigan, K.M.1    Johns, D.R.2
  • 18
    • 0028337837 scopus 로고
    • Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
    • Kellar-Wood H et al. (1994) Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Ann Neurol 36: 109-112.
    • (1994) Ann Neurol , vol.36 , pp. 109-112
    • Kellar-Wood, H.1
  • 19
    • 0028957580 scopus 로고
    • Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harboring the mitochondrial DNA 11778 mutation
    • Olsen NK et al. (1995) Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harboring the mitochondrial DNA 11778 mutation. Acta Neurol Scand 91: 326-329.
    • (1995) Acta Neurol Scand , vol.91 , pp. 326-329
    • Olsen, N.K.1
  • 20
    • 0028949749 scopus 로고
    • The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
    • Riordan-Eva P et al. (1995) The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain, 118: 319-337.
    • (1995) Brain , vol.118 , pp. 319-337
    • Riordan-Eva, P.1
  • 21
    • 0025312304 scopus 로고
    • Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein
    • Loveland B et al. (1990) Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein. Cell 60: 971-980.
    • (1990) Cell , vol.60 , pp. 971-980
    • Loveland, B.1
  • 22
    • 0025232653 scopus 로고
    • A mitochondiral encephalomyopathy with specific deficiencies of two respiratory chain polypeptides and a circulating auto-antibody to a mitochondrial matrix protein
    • Schapira AHV et al. (1990) A mitochondiral encephalomyopathy with specific deficiencies of two respiratory chain polypeptides and a circulating auto-antibody to a mitochondrial matrix protein. Brain 113: 419-432.
    • (1990) Brain , vol.113 , pp. 419-432
    • Schapira, A.H.V.1
  • 23
    • 0029041731 scopus 로고
    • Antibodies to human optic nerve in Leber's hereditary optic neuropathy
    • Smith PR et al. (1995) Antibodies to human optic nerve in Leber's hereditary optic neuropathy. J Neurol Sci 130: 134-138.
    • (1995) J Neurol Sci , vol.130 , pp. 134-138
    • Smith, P.R.1
  • 24
    • 24344444167 scopus 로고
    • Characterization of the mitochondrial DNA in multiple sclerosis
    • in press
    • Kalman B et al. (1995) Characterization of the mitochondrial DNA in multiple sclerosis. J. Neurol Sci, in press.
    • (1995) J. Neurol Sci
    • Kalman, B.1
  • 25
    • 0026013435 scopus 로고
    • Parent child concordance in multiple sclerosis
    • Sadovnick AD et al. (1991) Parent child concordance in multiple sclerosis. Ann Neurol 29: 252-255.
    • (1991) Ann Neurol , vol.29 , pp. 252-255
    • Sadovnick, A.D.1
  • 26
    • 0028595987 scopus 로고
    • Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
    • Hanefeld FA et al. (1994) Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis. Neuropediatrics 25: 331.
    • (1994) Neuropediatrics , vol.25 , pp. 331
    • Hanefeld, F.A.1
  • 27
    • 0029279163 scopus 로고
    • Mitochondrial DNA mutations in multiple sclerosis
    • Kalman B et al. (1995) Mitochondrial DNA mutations in multiple sclerosis. Multiple Sclerosis 1: 32-36.
    • (1995) Multiple Sclerosis , vol.1 , pp. 32-36
    • Kalman, B.1
  • 28
    • 0026702249 scopus 로고
    • Leber's hereditary optic neuropathy: A model for mitochondrial neurodegenerative diseases
    • Brown MD et al. (1992) Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases. FASEB J 6: 2791-2799.
    • (1992) FASEB J , vol.6 , pp. 2791-2799
    • Brown, M.D.1
  • 29
    • 0019423856 scopus 로고
    • Sequence and organization of the human mitochondrial genome
    • Anderson S et al. (1981) Sequence and organization of the human mitochondrial genome. Nature 290: 457-464.
    • (1981) Nature , vol.290 , pp. 457-464
    • Anderson, S.1
  • 30
    • 0003215976 scopus 로고
    • Peculiar features and evolution of mitochondrial genome in mammals
    • DiMauro S, Wallace DC (eds) Raven Press: NY.
    • Saccone C et al. (1993) Peculiar features and evolution of mitochondrial genome in mammals. In: Mitochondrial DNA in human pathology. DiMauro S, Wallace DC (eds) Raven Press: NY. pp 27-37.
    • (1993) Mitochondrial DNA in Human Pathology , pp. 27-37
    • Saccone, C.1
  • 31
    • 0028095263 scopus 로고
    • MtDNA and the origin of Caucasians: Identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region
    • Torroni A et al. (1994) mtDNA and the origin of Caucasians: Identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet 55: 760-776.
    • (1994) Am J Hum Genet , vol.55 , pp. 760-776
    • Torroni, A.1
  • 32
  • 33
    • 0020686503 scopus 로고
    • New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
    • Poser CM et al. (1983) New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann Neruol 13: 227-231.
    • (1983) Ann Neruol , vol.13 , pp. 227-231
    • Poser, C.M.1
  • 34
    • 0029017083 scopus 로고
    • Length heteroplasmy in the first hypervariable segment of the human mtDNA control region
    • Bendall KE, Sykes BC. (1995) Length heteroplasmy in the first hypervariable segment of the human mtDNA control region. Am J Hum Genet 57: 248-256.
    • (1995) Am J Hum Genet , vol.57 , pp. 248-256
    • Bendall, K.E.1    Sykes, B.C.2
  • 35
    • 0026036025 scopus 로고
    • Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
    • Johns DR, Berman J. (1991) Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy. Biochem and Biophys Res Com 174: 1324-1330.
    • (1991) Biochem and Biophys Res Com , vol.174 , pp. 1324-1330
    • Johns, D.R.1    Berman, J.2
  • 36
    • 0025308462 scopus 로고
    • Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA
    • Horai S, Hayasaka K. (1990) Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA. Am J Hum Genet 46: 828-842.
    • (1990) Am J Hum Genet , vol.46 , pp. 828-842
    • Horai, S.1    Hayasaka, K.2
  • 37
    • 0028905461 scopus 로고
    • Demographic history of India and mtDNA-sequence diversity
    • Mountain JL et al. (1995) Demographic history of India and mtDNA-sequence diversity. Am J Hum Genet 56: 979-992.
    • (1995) Am J Hum Genet , vol.56 , pp. 979-992
    • Mountain, J.L.1
  • 38
    • 0026071738 scopus 로고
    • Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes
    • Stoneking M et al. (1991) Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes. Am J Hum Genet 48: 370-382.
    • (1991) Am J Hum Genet , vol.48 , pp. 370-382
    • Stoneking, M.1
  • 39
    • 0026063965 scopus 로고
    • Branching pattern in the evolutionary tree for human mitochondrial DNA
    • DiRienzo A, Wilson A. (1991) Branching pattern in the evolutionary tree for human mitochondrial DNA. Proc Natl Acad Sci 88: 1597-1601.
    • (1991) Proc Natl Acad Sci , vol.88 , pp. 1597-1601
    • DiRienzo, A.1    Wilson, A.2
  • 40
    • 0027496282 scopus 로고
    • The application of mitochondrial DNA typing to the study of white Caucasian genetic identification
    • Piercy R et al. (1993) The application of mitochondrial DNA typing to the study of white Caucasian genetic identification. Int J Legal Med 106: 85-90.
    • (1993) Int J Legal Med , vol.106 , pp. 85-90
    • Piercy, R.1
  • 41
    • 0028788493 scopus 로고
    • Phylogenetic analysis of Caucasian 11778-positive and 11778-negative Leber's hereditary optic neuropathy patients indicates multiple independent occurrences of the common primary mitochondrial DNA mutations
    • Brown MD et al. (1995) Phylogenetic analysis of Caucasian 11778-positive and 11778-negative Leber's hereditary optic neuropathy patients indicates multiple independent occurrences of the common primary mitochondrial DNA mutations. Hum Mut 6: 311-325.
    • (1995) Hum Mut , vol.6 , pp. 311-325
    • Brown, M.D.1
  • 42
    • 0028928397 scopus 로고
    • Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
    • Howell N et al. (1995) Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees. Genetics 140: 285-302.
    • (1995) Genetics , vol.140 , pp. 285-302
    • Howell, N.1
  • 43
    • 0026531040 scopus 로고
    • Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy
    • Brown MD et al. (1992) Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics 130: 163-173.
    • (1992) Genetics , vol.130 , pp. 163-173
    • Brown, M.D.1
  • 44
    • 0027200741 scopus 로고
    • Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
    • Shoffner JM et al. (1993) Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 17: 171-184.
    • (1993) Genomics , vol.17 , pp. 171-184
    • Shoffner, J.M.1
  • 45
    • 0029091194 scopus 로고
    • A mitochondrial DNA clone is associated with increased risk for Alzheimer disease
    • Hutchin T, Cortopassi G. (1995) A mitochondrial DNA clone is associated with increased risk for Alzheimer disease. Proc Natl Acad Sci 92: 6892-6895.
    • (1995) Proc Natl Acad Sci , vol.92 , pp. 6892-6895
    • Hutchin, T.1    Cortopassi, G.2
  • 46
    • 0027226069 scopus 로고
    • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
    • Prezant TR et al. (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 4: 289-294.
    • (1993) Nat Genet , vol.4 , pp. 289-294
    • Prezant, T.R.1
  • 47
    • 0029153643 scopus 로고
    • No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan
    • Nishimura M et al. (1995) No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan. Neurology 45: 1333-1334.
    • (1995) Neurology , vol.45 , pp. 1333-1334
    • Nishimura, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.