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Volumn 49, Issue 4, 1997, Pages 907-908

New techniques for investigating mitochondrial DNA in neurodegenerative diseases

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0031253876     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.49.4.907     Document Type: Editorial
Times cited : (7)

References (12)
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  • 2
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    • Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation.
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  • 3
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    • MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA (lys) and premature translation termination.
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  • 4
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    • Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy.
    • Hofhaus G, Johns DR, Hurko O, Attardi G, Chomyn A. Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy. J Biol Chem 1996;271:13155-13161.
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    • Hofhaus, G.1    Johns, D.R.2    Hurko, O.3    Attardi, G.4    Chomyn, A.5
  • 5
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    • Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA (leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke like episodes.
    • King MP, Koga Y, Davidson M, Schon EA. Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA (leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke like episodes. Mol Cell Biol 1992;12:480-490.
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  • 6
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    • Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.
    • Jun AS, Trounce IA, Brown MD, Shoffner JM, Wallace DC. Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia. Mol Cell Biol 1996;16:771-777.
    • (1996) Mol Cell Biol , vol.16 , pp. 771-777
    • Jun, A.S.1    Trounce, I.A.2    Brown, M.D.3    Shoffner, J.M.4    Wallace, D.C.5
  • 7
    • 0027936218 scopus 로고
    • Cytoplasmic transfer of mtDNA nt 8993 G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in stage III respiration and ADP/O ratio.
    • Trounce I, Neill S, Wallace DC. Cytoplasmic transfer of mtDNA nt 8993 → G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in stage III respiration and ADP/O ratio. Proc Natl Acad Sci USA 1994;91:8334-8338.
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  • 8
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    • Laderman KA, Penny JR, Mazzucchelli F, Bresolin N, Scarlato G, Attardi G. Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells. J Biol Chem 1996;271:15891-15897.
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  • 9
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    • Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer's disease.
    • Davis RE, Miller S, Hermstadt C, et al. Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer's disease. Proc Natl Acad Sci USA 1997;94:4526-4531.
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.