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Volumn 140, Issue 1-2, 1996, Pages 75-84

Characterization of the mitochondrial DNA in patients with multiple sclerosis

Author keywords

Genetic susceptibility; MtDNA variant; Multiple sclerosis

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0030247011     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-510X(96)00112-8     Document Type: Article
Times cited : (45)

References (53)
  • 1
    • 0018394631 scopus 로고
    • A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis
    • Allen, I.V. and McKeon, S.R. (1979) A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis. J. Neurol. Sci., 41: 81-91.
    • (1979) J. Neurol. Sci. , vol.41 , pp. 81-91
    • Allen, I.V.1    McKeon, S.R.2
  • 3
    • 0019983804 scopus 로고
    • Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome
    • Anderson, S., DeBruijn, M.H.L., Coulson, A.R., Eperon, I.C., Sanger, F. and Young, I.G. (1982) Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome. J. Mol. Biol., 156: 683-717.
    • (1982) J. Mol. Biol. , vol.156 , pp. 683-717
    • Anderson, S.1    DeBruijn, M.H.L.2    Coulson, A.R.3    Eperon, I.C.4    Sanger, F.5    Young, I.G.6
  • 4
    • 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, S.S., Biddison, W.E., McFarlin, D.E., McFarland, H.F. and Hood, L.E. (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    Biddison, W.E.2    McFarlin, D.E.3    McFarland, H.F.4    Hood, L.E.5
  • 8
    • 0026702249 scopus 로고
    • Leber's hereditary optic neuropathy: A model for mitochondrial neurodegenerative diseases
    • Brown, M.D., Voljavec, A.S., Lott, M.T., MacDonald, I. and Wallace, D.C. (1992a) 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    Voljavec, A.S.2    Lott, M.T.3    MacDonald, I.4    Wallace, D.C.5
  • 9
    • 0026531040 scopus 로고
    • Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy
    • Brown, M.D., Voljavec, A.S., Lott, M.T., Torroni, A., Yang, C.C. and Wallace, D.C. (1992b) 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    Voljavec, A.S.2    Lott, M.T.3    Torroni, A.4    Yang, C.C.5    Wallace, D.C.6
  • 10
    • 0002699021 scopus 로고
    • A sex-linked heredo-degenerative neurological disorder, associated with Leber's optic atrophy. Part I. Clinical studies
    • Bruyn, G.W. and Went, L.N. (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    Went, L.N.2
  • 11
    • 0029014947 scopus 로고
    • Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis
    • Chalmers, R.M., Robertson, N., Kellar-Wood, H., Compston, D.A.S. and Harding, A.E. (1995) Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis. J. Neurol., 242: 332-334.
    • (1995) J. Neurol. , vol.242 , pp. 332-334
    • Chalmers, R.M.1    Robertson, N.2    Kellar-Wood, H.3    Compston, D.A.S.4    Harding, A.E.5
  • 12
    • 0022271984 scopus 로고
    • The mitochondrial DNA molecule of Drosophila yakuba: Nucleotide sequence, gene organization and genetic code
    • Clary, D.O. and Wolstenholme, D.R. (1985) The mitochondrial DNA molecule of Drosophila yakuba: nucleotide sequence, gene organization and genetic code. J. Mol. Evol., 22: 252-271.
    • (1985) J. Mol. Evol. , vol.22 , pp. 252-271
    • Clary, D.O.1    Wolstenholme, D.R.2
  • 13
    • 0026049670 scopus 로고
    • HLA-DR and -DQ allelic sequences in multiple sclerosis patients are identical to those found in the general population
    • Cowan, E.P., Pierce, M.L., McFarland, H.F. and McFarlin, D.E. (1991) HLA-DR and -DQ allelic sequences in multiple sclerosis patients are identical to those found in the general population. Hum. Immunol., 32: 203-210.
    • (1991) Hum. Immunol. , vol.32 , pp. 203-210
    • Cowan, E.P.1    Pierce, M.L.2    McFarland, H.F.3    McFarlin, D.E.4
  • 14
    • 0001174007 scopus 로고
    • Leber's optic atrophy and its relation to the heredo-familial ataxias
    • Ferguson, F.R. and 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
  • 15
    • 0029075525 scopus 로고
    • A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis
    • Filippi, M., Campi, A., Dousset, V., Baratti, C., Martinelli, V., Canal, N., Scotti, G. and Comi, G. (1995) A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis. Neurology, 45: 478-482.
    • (1995) Neurology , vol.45 , pp. 478-482
    • Filippi, M.1    Campi, A.2    Dousset, V.3    Baratti, C.4    Martinelli, V.5    Canal, N.6    Scotti, G.7    Comi, G.8
  • 16
    • 0027731794 scopus 로고
    • Association of the 11778 mitochondrial DNA mutation and demyelinating disease
    • Flanigan, K.M. and Johns, D.R. (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
  • 17
    • 0028595987 scopus 로고
    • Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
    • Hanefeld, F.A., Ernst, B.P., Wilichowski, E. and Cristen, H.-J. (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    Ernst, B.P.2    Wilichowski, E.3    Cristen, H.-J.4
  • 18
    • 0026782507 scopus 로고
    • Occurrence of multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
    • Harding, A.E., Sweeney, M.G., Miller, D.H., Mumford, C.J., Kellar-Wood, H., Menard, D., McDonald, W.I. and Compston, D.A.S. (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    Sweeney, M.G.2    Miller, D.H.3    Mumford, C.J.4    Kellar-Wood, H.5    Menard, D.6    McDonald, W.I.7    Compston, D.A.S.8
  • 19
    • 0001782589 scopus 로고
    • HLA-Dw2 in multiple sclerosis: A world-wide association and a close segregation with disease in multiplex families
    • Hillert, J., Kall, T. and Ollerup, O. (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    Kall, T.2    Ollerup, O.3
  • 20
    • 0025897119 scopus 로고
    • Leber hereditary optic neuropathy: Involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation
    • Howell, N., Kubacka, I., Xu, M. and McCullough, D.A, (1991) Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation. Am. J. Hum. Genet., 48: 935-942.
    • (1991) Am. J. Hum. Genet. , vol.48 , pp. 935-942
    • Howell, N.1    Kubacka, I.2    Xu, M.3    McCullough, D.A.4
  • 24
    • 0026757115 scopus 로고
    • An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
    • Johns, D.R., Neufeld, M.J. and Park, R.D. (1992) An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy. Biochem. Biophys. Res. Commun., 187: 1551-1557.
    • (1992) Biochem. Biophys. Res. Commun. , vol.187 , pp. 1551-1557
    • Johns, D.R.1    Neufeld, M.J.2    Park, R.D.3
  • 25
    • 0028342847 scopus 로고
    • A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene with maternally inherited Leber hereditary optic neuropathy and dystonia
    • Jun, A.S., Brown, M.D. and Wallace, D.C. (1994) A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene with maternally inherited Leber hereditary optic neuropathy and dystonia. Proc. Natl. Acad. Sci. USA, 91: 6206-6210.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 6206-6210
    • Jun, A.S.1    Brown, M.D.2    Wallace, D.C.3
  • 26
    • 0029279163 scopus 로고
    • Mitochondrial DNA mutations in multiple sclerosis
    • Kalman, B., Lublin, F.D. and Alder, H. (1995) Mitochondrial DNA mutations in multiple sclerosis. Multiple Sclerosis, 1: 32-36.
    • (1995) Multiple Sclerosis , vol.1 , pp. 32-36
    • Kalman, B.1    Lublin, F.D.2    Alder, H.3
  • 27
    • 0028337837 scopus 로고
    • Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
    • Kellar-Wood, H., Robertson, N., Govan, G.G., Compston, D.A.S. and Harding, A.E. (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    Robertson, N.2    Govan, G.G.3    Compston, D.A.S.4    Harding, A.E.5
  • 29
    • 0025312304 scopus 로고
    • Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein
    • Loveland, B., Wang, C.R., Yonekawa, H., Hermel, E. and Lindahl, K.F. (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    Wang, C.R.2    Yonekawa, H.3    Hermel, E.4    Lindahl, K.F.5
  • 30
    • 0002387271 scopus 로고
    • Leber's disease. A genealogic, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families
    • Lundsgaard, R. (1994) Leber's disease. A genealogic, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families. Acta Ophthalmol. (Suppl.), 21: 300-306.
    • (1994) Acta Ophthalmol. , vol.21 , Issue.SUPPL. , pp. 300-306
    • Lundsgaard, R.1
  • 31
    • 0026609572 scopus 로고
    • Discordance of the T-cell receptor alpha-chain gene in familial multiple sclerosis
    • Lynch, S.G., Rose, J.W., Petajan, J.H. and Leppert, M. (1992) Discordance of the T-cell receptor alpha-chain gene in familial multiple sclerosis. Neurology, 42: 839-844.
    • (1992) Neurology , vol.42 , pp. 839-844
    • Lynch, S.G.1    Rose, J.W.2    Petajan, J.H.3    Leppert, M.4
  • 33
    • 0026746739 scopus 로고
    • A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology
    • Mackey, D. and Howell, N. (1992) A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology. Am. J. Hum. Genet., 51: 1218-1228.
    • (1992) Am. J. Hum. Genet. , vol.51 , pp. 1218-1228
    • Mackey, D.1    Howell, N.2
  • 34
    • 0026409821 scopus 로고
    • Normal variants of human mitochondrial DNA and translation products: The building of a reference data base
    • Marzuki, S., Noer, A.S., Letrit, P., Thyagarajan, D., Kapsa, R., Utthanaphol, P. and Byrne, E. (1991) Normal variants of human mitochondrial DNA and translation products: the building of a reference data base. Hum. Genet., 88: 139-145.
    • (1991) Hum. Genet. , vol.88 , pp. 139-145
    • Marzuki, S.1    Noer, A.S.2    Letrit, P.3    Thyagarajan, D.4    Kapsa, R.5    Utthanaphol, P.6    Byrne, E.7
  • 35
    • 0001296348 scopus 로고
    • Reply to Howell et al: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA
    • Marzuki, S., Letrit, P., Noer, A.S., Kapsa, R., Sudoyo, R.M.I., Byrne, E. and Thyagarajan, D. (1992) Reply to Howell et al: the need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA. Am. J. Hum. Genet. 50: 1337-1340.
    • (1992) Am. J. Hum. Genet. , vol.50 , pp. 1337-1340
    • Marzuki, S.1    Letrit, P.2    Noer, A.S.3    Kapsa, R.4    Sudoyo, R.M.I.5    Byrne, E.6    Thyagarajan, D.7
  • 36
    • 0027180961 scopus 로고
    • Leber's hereditary optic neuropathy. New genetic considerations. Review article
    • Newman, N.J. (1993) Leber's hereditary optic neuropathy. New genetic considerations. Review article. Arch. Neurol., 50: 540-547.
    • (1993) Arch. Neurol. , vol.50 , pp. 540-547
    • Newman, N.J.1
  • 38
    • 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, N.K., Hansen, A.W., Norby, S., Edal, A.L., Jorgensen, J.R. and Rosenberg, T. (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    Hansen, A.W.2    Norby, S.3    Edal, A.L.4    Jorgensen, J.R.5    Rosenberg, T.6
  • 39
    • 0019424530 scopus 로고
    • Immunoglobulin G heavy chain (Gm) allotypes in multiple sclerosis
    • Pandey, J.P., Goust, J.M. and Salier, J.P. (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    Goust, J.M.2    Salier, J.P.3
  • 42
    • 0028949749 scopus 로고
    • The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mulation
    • Riordan-Eva, P., Sanders, M.D., Govan, G.G., Sweeney, M.G., Da Costa, J. and Harding, A.E. (1995) The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mulation. Brain, 118: 319-337.
    • (1995) Brain , vol.118 , pp. 319-337
    • Riordan-Eva, P.1    Sanders, M.D.2    Govan, G.G.3    Sweeney, M.G.4    Da Costa, J.5    Harding, A.E.6
  • 43
    • 0026013435 scopus 로고
    • Parent child concordance in multiple sclerosis
    • Sadovnick, A.D., Bulman, D. and Ebers, G.C. (1991) Parent child concordance in multiple sclerosis. Ann. Neurol., 29: 252-255.
    • (1991) Ann. Neurol. , vol.29 , pp. 252-255
    • Sadovnick, A.D.1    Bulman, D.2    Ebers, G.C.3
  • 44
    • 0025232653 scopus 로고
    • A mitochondrial encephalomyopathy with specific deficiencies of two respiratory chain polypeptides and a circulating auto-antibody to a mitochondrial matrix protein
    • Schapira, A.H.V., Cooper, J.M., Manneschi, L., Vital, C., Morgan-Hughes, J.A. and Clark, J.B. (1990) A mitochondrial 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    Cooper, J.M.2    Manneschi, L.3    Vital, C.4    Morgan-Hughes, J.A.5    Clark, J.B.6
  • 45
    • 0024406282 scopus 로고
    • A susceptibility locus for multiple sclerosis is linked to the T cell receptor β chain complex
    • Seboun, E., Robinson, M.A., Doolittle, T.H., Ciulla, T.A., Kindt, T.J. and Hauser, S.L. (1989) A susceptibility locus for multiple sclerosis is linked to the T cell receptor β chain complex. Cell, 57: 1095-1100.
    • (1989) Cell , vol.57 , pp. 1095-1100
    • Seboun, E.1    Robinson, M.A.2    Doolittle, T.H.3    Ciulla, T.A.4    Kindt, T.J.5    Hauser, S.L.6
  • 49
    • 0026670087 scopus 로고
    • Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene
    • Tienari, P.J., Wikstrom, J., Sajantila, A., Palo, J. and Peltonen, L. (1992) Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene. Lancet, 340: 987-991.
    • (1992) Lancet , vol.340 , pp. 987-991
    • Tienari, P.J.1    Wikstrom, J.2    Sajantila, A.3    Palo, J.4    Peltonen, L.5
  • 53
    • 0021132161 scopus 로고
    • Is the myelin membrane abnormal in multiple sclerosis?
    • Wood, D.D. and Moscarello, M.A. (1984) Is the myelin membrane abnormal in multiple sclerosis? J. Membr. Biol., 79: 195-201.
    • (1984) J. Membr. Biol. , vol.79 , pp. 195-201
    • Wood, D.D.1    Moscarello, M.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.