메뉴 건너뛰기




Volumn 253, Issue 1-2, 1996, Pages 182-188

Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathies

Author keywords

Differentiation; Mitochondrial DNA; Muscle cells; Muscular diseases

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0029972282     PISSN: 00268925     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004380050311     Document Type: Article
Times cited : (7)

References (22)
  • 2
    • 0023277102 scopus 로고
    • Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: Morphological, immunological and biochemical studies in muscle biopsies and autopsy tissues
    • Bresolin N, Moggio M, Bet L, Gallanti A, Prelle A, Nobile-Orazio E, Adobatti L, Ferrante C, Pellegrini G, Searlato G (1987) Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological and biochemical studies in muscle biopsies and autopsy tissues. Ann Neurol 121:564-572
    • (1987) Ann Neurol , vol.121 , pp. 564-572
    • Bresolin, N.1    Moggio, M.2    Bet, L.3    Gallanti, A.4    Prelle, A.5    Nobile-Orazio, E.6    Adobatti, L.7    Ferrante, C.8    Pellegrini, G.9    Searlato, G.10
  • 3
    • 0028286006 scopus 로고
    • Molecular basis of mitochondrial DNA disease
    • Brown MD, Wallace DC (1994) Molecular basis of mitochondrial DNA disease. J Bioenerg Biomembr 26:273-289
    • (1994) J Bioenerg Biomembr , vol.26 , pp. 273-289
    • Brown, M.D.1    Wallace, D.C.2
  • 4
    • 0019768234 scopus 로고
    • Mitochondrial proliferation during myogencsis
    • Brunk CF (1981) Mitochondrial proliferation during myogencsis. Exp Cell Res 136:305-309
    • (1981) Exp Cell Res , vol.136 , pp. 305-309
    • Brunk, C.F.1
  • 5
    • 0025765287 scopus 로고
    • Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy
    • Cormier V, Rötig A, Tardieu M, Colonna M, Saudubray J-M, Munnich A (1991) Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy. Am J Hum Genet 48:643-648
    • (1991) Am J Hum Genet , vol.48 , pp. 643-648
    • Cormier, V.1    Rötig, A.2    Tardieu, M.3    Colonna, M.4    Saudubray, J.-M.5    Munnich, A.6
  • 8
    • 0021260779 scopus 로고
    • Comparison between the growth pattern of cell cultures from normal and Duchenne dystrophy muscle
    • Delaporte C, Dehaupas M, Fardeau M (1984) Comparison between the growth pattern of cell cultures from normal and Duchenne dystrophy muscle. J Neurol Sci 64: 149-160
    • (1984) J Neurol Sci , vol.64 , pp. 149-160
    • Delaporte, C.1    Dehaupas, M.2    Fardeau, M.3
  • 9
    • 0025836655 scopus 로고
    • Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochonrial DNA results in mitochondrial dysfunction
    • Hayashi J-I, Ohta S, Kikuchi A, Takemitsu M, Goto Y-I, Nonaka I (1991) Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochonrial DNA results in mitochondrial dysfunction. Proc Natl Acad Sci USA 88: 10614-10618
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 10614-10618
    • Hayashi, J.-I.1    Ohta, S.2    Kikuchi, A.3    Takemitsu, M.4    Goto, Y.-I.5    Nonaka, I.6
  • 10
    • 0028217896 scopus 로고
    • Steady state levels of mitochondrial and nuclear oxidative phosphorylation transcripts in Kearns-Sayre syndrome
    • Heddi A, Lestienne P, Wallace DC, Stepien G (1994) Steady state levels of mitochondrial and nuclear oxidative phosphorylation transcripts in Kearns-Sayre syndrome. Biochim Biophys Acta 1226:206-212
    • (1994) Biochim Biophys Acta , vol.1226 , pp. 206-212
    • Heddi, A.1    Lestienne, P.2    Wallace, D.C.3    Stepien, G.4
  • 11
    • 0023665343 scopus 로고
    • A rapid method for the purification of DNA from blood
    • Jeanpierre M (1987) A rapid method for the purification of DNA from blood. Nucleic Acids Res 15:9611
    • (1987) Nucleic Acids Res , vol.15 , pp. 9611
    • Jeanpierre, M.1
  • 12
    • 0021835938 scopus 로고
    • Shuttling of integrated vectors from mammalian cells to E. coli is mediated by head-to-tail multimeric inserts
    • Luftalla G, Blanc H, Bertoloiti R (1985) Shuttling of integrated vectors from mammalian cells to E. coli is mediated by head-to-tail multimeric inserts. Somat Cell Mol Genet 11:223-238
    • (1985) Somat Cell Mol Genet , vol.11 , pp. 223-238
    • Luftalla, G.1    Blanc, H.2    Bertoloiti, R.3
  • 15
    • 0000163138 scopus 로고
    • Isolation of high-molecular-weight DNA from mammalian cells
    • Sambrook J, Fritsch EF, Maniatis T (eds) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
    • Sambrook J, Fritsch EF, Maniatis T (1989) Isolation of high-molecular-weight DNA from mammalian cells. In: Sambrook J, Fritsch EF, Maniatis T (eds) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, pp 9.16-9.19
    • (1989) Molecular Cloning: A Laboratory Manual, 2nd Edn. , pp. 916-919
    • Sambrook, J.1    Fritsch, E.F.2    Maniatis, T.3
  • 16
    • 0024317560 scopus 로고
    • Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: A slip-replication model and metabolic therapy
    • Shoffner JM, Lott MT, Voljavec AS, Soueidan SA, Costigan DA, Wallace DC (1989) Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. Proc Nail Acad Sci USA 86:7952-7956
    • (1989) Proc Nail Acad Sci USA , vol.86 , pp. 7952-7956
    • Shoffner, J.M.1    Lott, M.T.2    Voljavec, A.S.3    Soueidan, S.A.4    Costigan, D.A.5    Wallace, D.C.6
  • 17
    • 0025276996 scopus 로고
    • Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle liber segments in mitochondrial disease
    • Shoubridge HA, Karpati G, Hastings KEM (1990) Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle liber segments in mitochondrial disease. Cell 62:43-49
    • (1990) Cell , vol.62 , pp. 43-49
    • Shoubridge, H.A.1    Karpati, G.2    Hastings, K.E.M.3
  • 18
    • 0026637067 scopus 로고
    • Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive ophthalmoplegia
    • Suomalainen A, Majander A, Haltia M, Somer H, Lönnquist J, Savontaus ML, Peltonen L (1992) Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive ophthalmoplegia. J Clin Invest 90:61-66
    • (1992) J Clin Invest , vol.90 , pp. 61-66
    • Suomalainen, A.1    Majander, A.2    Haltia, M.3    Somer, H.4    Lönnquist, J.5    Savontaus, M.L.6    Peltonen, L.7
  • 20
    • 0026624980 scopus 로고
    • Diseases of the mitochondrial DNA
    • Wallace DC (1992) Diseases of the mitochondrial DNA. Annu Rev Biochem 61:1175-1212
    • (1992) Annu Rev Biochem , vol.61 , pp. 1175-1212
    • Wallace, D.C.1
  • 21
    • 0026715879 scopus 로고
    • Nucleus-driven mutations of human mitochondrial DNA
    • Zeviani M (1992) Nucleus-driven mutations of human mitochondrial DNA. J Inherit Metab Dis 15:456-471
    • (1992) J Inherit Metab Dis , vol.15 , pp. 456-471
    • Zeviani, M.1
  • 22
    • 0024601360 scopus 로고
    • An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
    • Zeviani M, Servidei S, Gellera C, Bertini E, DiMauro S, DiDonato S (1989) An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region. Nature 339:309-311
    • (1989) Nature , vol.339 , pp. 309-311
    • Zeviani, M.1    Servidei, S.2    Gellera, C.3    Bertini, E.4    DiMauro, S.5    DiDonato, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.