메뉴 건너뛰기




Volumn 8, Issue 5, 2009, Pages 566-572

Quantification of mitochondrial DNA mutation load

Author keywords

Ageing; Cloning; Colon; Human; Mitochondria; Mitochondrial DNA; Mutation load; Polymerase chain reaction

Indexed keywords

MITOCHONDRIAL DNA;

EID: 72649097680     PISSN: 14749718     EISSN: 14749726     Source Type: Journal    
DOI: 10.1111/j.1474-9726.2009.00505.x     Document Type: Article
Times cited : (35)

References (24)
  • 2
    • 0026469073 scopus 로고
    • Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing
    • Cooper JM, Mann VM, Schapira AH (1992) Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing. J. Neurol. Sci. 113, 91-98.
    • (1992) J. Neurol. Sci. , vol.113 , pp. 91-98
    • Cooper, J.M.1    Mann, V.M.2    Schapira, A.H.3
  • 3
    • 0025674177 scopus 로고
    • Detection of a specific mitochondrial DNA deletion in tissues of older humans
    • Cortopassi GA, Arnheim N (1990) Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res. 18, 6927-6933.
    • (1990) Nucleic Acids Res. , vol.18 , pp. 6927-6933
    • Cortopassi, G.A.1    Arnheim, N.2
  • 5
    • 0037110426 scopus 로고    scopus 로고
    • Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients
    • Del Bo R, Bordoni A, Martinelli Boneschi F, Crimi M, Sciacco M, Bresolin N, Scarlato G, Comi GP (2002) Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients. J. Neurol. Sci. 202, 85-91.
    • (2002) J. Neurol. Sci. , vol.202 , pp. 85-91
    • Del Bo, R.1    Bordoni, A.2    Martinelli Boneschi, F.3    Crimi, M.4    Sciacco, M.5    Bresolin, N.6    Scarlato, G.7    Comi, G.P.8
  • 8
    • 25144461054 scopus 로고    scopus 로고
    • Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations
    • Kraytsberg Y, Khrapko K (2005) Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations. Expert Rev. Mol. Diagn. 5, 809-815.
    • (2005) Expert Rev. Mol. Diagn. , vol.5 , pp. 809-815
    • Kraytsberg, Y.1    Khrapko, K.2
  • 10
    • 74249099088 scopus 로고    scopus 로고
    • Are somatic mitochondrial DNA mutations relevant to our health? A challenge for mutation analysis techniques
    • Kraytsberg Y, Nicholas A, Khrapko K (2007). Are somatic mitochondrial DNA mutations relevant to our health? A challenge for mutation analysis techniquesExpert Opin. Med. Diagn. 1, 109-116.
    • (2007) Expert Opin. Med. Diagn. , vol.1 , pp. 109-116
    • Kraytsberg, Y.1    Nicholas, A.2    Khrapko, K.3
  • 11
    • 56249114494 scopus 로고    scopus 로고
    • Single molecule PCR in mtDNA mutational analysis: genuine mutations vs. damage bypass-derived artifacts
    • Kraytsberg Y, Nicholas A, Caro P, Khrapko K (2008) Single molecule PCR in mtDNA mutational analysis: genuine mutations vs. damage bypass-derived artifacts. Methods 46, 269-273.
    • (2008) Methods , vol.46 , pp. 269-273
    • Kraytsberg, Y.1    Nicholas, A.2    Caro, P.3    Khrapko, K.4
  • 14
    • 0013957553 scopus 로고
    • The circularity of mitochondrial DNA
    • Nass MM (1966) The circularity of mitochondrial DNA. Proc. Natl Acad. Sci. USA 56, 1215-1222.
    • (1966) Proc. Natl Acad. Sci. USA , vol.56 , pp. 1215-1222
    • Nass, M.M.1
  • 16
    • 0024459635 scopus 로고
    • Methods of microphotometric assay of succinate dehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle
    • Old SL, Johnson MA (1989) Methods of microphotometric assay of succinate dehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle. Histochem. J. 21, 545-555.
    • (1989) Histochem. J. , vol.21 , pp. 545-555
    • Old, S.L.1    Johnson, M.A.2
  • 18
    • 4644351698 scopus 로고    scopus 로고
    • High frequency of mitochondrial complex I mutations in Parkinson's disease and aging
    • Smigrodzki R, Parks J, Parker WD (2004) High frequency of mitochondrial complex I mutations in Parkinson's disease and aging. Neurobiol. Aging 25, 1273-1281.
    • (2004) Neurobiol. Aging , vol.25 , pp. 1273-1281
    • Smigrodzki, R.1    Parks, J.2    Parker, W.D.3
  • 19
    • 17744393686 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations in human disease
    • Taylor RW, Turnbull DM (2005) Mitochondrial DNA mutations in human disease. Nat Rev Genet 6, 389-402.
    • (2005) Nat Rev Genet , vol.6 , pp. 389-402
    • Taylor, R.W.1    Turnbull, D.M.2
  • 24
    • 0036073133 scopus 로고    scopus 로고
    • Pattern of organization of human mitochondrial pseudogenes in the nuclear genome
    • Woischnik M, Moraes CT (2002) Pattern of organization of human mitochondrial pseudogenes in the nuclear genome. Genome Res. 12, 885-893.
    • (2002) Genome Res. , vol.12 , pp. 885-893
    • Woischnik, M.1    Moraes, C.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.