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Volumn 54, Issue 4, 2003, Pages 521-524

Genotypes from patients indicate no paternal mitochondrial DNA contribution

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0141819161     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10673     Document Type: Article
Times cited : (66)

References (16)
  • 2
    • 0033862962 scopus 로고    scopus 로고
    • The epidemiology of pathogenic mitochondrial DNA mutations
    • Chinnery PF, Johnson MA, Wardell TM, et al. The epidemiology of pathogenic mitochondrial DNA mutations. Ann Neurol 2000;48:188-193.
    • (2000) Ann Neurol , vol.48 , pp. 188-193
    • Chinnery, P.F.1    Johnson, M.A.2    Wardell, T.M.3
  • 4
    • 0037158599 scopus 로고    scopus 로고
    • Paternal inheritance of mitochondrial DNA
    • Schwartz M, Vissing J. Paternal inheritance of mitochondrial DNA. N Engl J Med 2002;347:576-580.
    • (2002) N Engl J Med , vol.347 , pp. 576-580
    • Schwartz, M.1    Vissing, J.2
  • 5
    • 0035172154 scopus 로고    scopus 로고
    • Analysis of European mtDNAs for recombination
    • Elson JL, Andrews RM, Chinnery PF, et al. Analysis of European mtDNAs for recombination. Am J Hum Genet 2001;68: 145-153.
    • (2001) Am J Hum Genet , vol.68 , pp. 145-153
    • Elson, J.L.1    Andrews, R.M.2    Chinnery, P.F.3
  • 6
    • 0037137561 scopus 로고    scopus 로고
    • Paternal inheritance of mitochondrial DNA
    • Vissing J, Schwartz M. Paternal inheritance of mitochondrial DNA. N Engl J Med 2002;347:2081-2082.
    • (2002) N Engl J Med , vol.347 , pp. 2081-2082
    • Vissing, J.1    Schwartz, M.2
  • 7
    • 0019423856 scopus 로고
    • Sequence and organization of the human mitochondrial genome
    • Anderson S, Bankier AT, Barrell BG, et al. Sequence and organization of the human mitochondrial genome. Nature 1981; 290:457-465.
    • (1981) Nature , vol.290 , pp. 457-465
    • Anderson, S.1    Bankier, A.T.2    Barrell, B.G.3
  • 8
    • 0032868141 scopus 로고    scopus 로고
    • Reanalysis and revision of the Cambridge Reference Sequence
    • Andrews RM, Kubacka I, Chinnery PF, et al. Reanalysis and revision of the Cambridge Reference Sequence. Nat Genet 1999;23:147.
    • (1999) Nat Genet , vol.23 , pp. 147
    • Andrews, R.M.1    Kubacka, I.2    Chinnery, P.F.3
  • 9
    • 0035432034 scopus 로고    scopus 로고
    • The determination of complete human mitochondrial DNA sequences in single cells: Implications for the study of somatic mitochondrial DNA point mutations
    • Taylor RW, Taylor GA, Durham SE, Turnbull DM. The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations. Nucleic Acids Res 2001;29: E74-4.
    • (2001) Nucleic Acids Res , vol.29
    • Taylor, R.W.1    Taylor, G.A.2    Durham, S.E.3    Turnbull, D.M.4
  • 10
    • 0037171660 scopus 로고    scopus 로고
    • A high frequency of mtDNA polymorphisms in HeLa cell sublines
    • Herrnstadt C, Preston G, Andrews R, et al. A high frequency of mtDNA polymorphisms in HeLa cell sublines. Mutat Res 2002;501:19-28.
    • (2002) Mutat Res , vol.501 , pp. 19-28
    • Herrnstadt, C.1    Preston, G.2    Andrews, R.3
  • 11
    • 0034955881 scopus 로고    scopus 로고
    • Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene
    • Taylor RW, Singh-Kler R, Hayes CM, et al. Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene. Ann Neurol 2001;50: 104-107.
    • (2001) Ann Neurol , vol.50 , pp. 104-107
    • Taylor, R.W.1    Singh-Kler, R.2    Hayes, C.M.3
  • 12
    • 0037372985 scopus 로고    scopus 로고
    • The pedigree rate of sequence divergence in the human mitochondrial genome: There is a difference between phylogenetic and pedigree rates
    • Howell N, Smejkal CB, Mackey DA, et al. The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates. Am J Hum Genet 2003;72:659-670.
    • (2003) Am J Hum Genet , vol.72 , pp. 659-670
    • Howell, N.1    Smejkal, C.B.2    Mackey, D.A.3
  • 14
    • 0029658242 scopus 로고    scopus 로고
    • A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy
    • Fu K, Hartlen R, Johns T, et al. A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy. Hum Mol Genet 1996;5:1835-1840.
    • (1996) Hum Mol Genet , vol.5 , pp. 1835-1840
    • Fu, K.1    Hartlen, R.2    Johns, T.3
  • 15
    • 0031020420 scopus 로고    scopus 로고
    • A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
    • Weber K, Wilson JN, Taylor L, et al. A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle. Am J Hum Genet 1997;60:373-380.
    • (1997) Am J Hum Genet , vol.60 , pp. 373-380
    • Weber, K.1    Wilson, J.N.2    Taylor, L.3
  • 16
    • 0037322524 scopus 로고    scopus 로고
    • The epidemiology of Leber's hereditary optic neuropathy in the north east of England
    • Man PY, Griffiths PG, Brown DT, et al. The epidemiology of Leber's hereditary optic neuropathy in the north east of England. Am J Hum Genet 2003;72:333-339.
    • (2003) Am J Hum Genet , vol.72 , pp. 333-339
    • Man, P.Y.1    Griffiths, P.G.2    Brown, D.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.