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Volumn 14, Issue 6, 2001, Pages 777-781

Mitochondrial oxidative phosphorylation system assembly in man: Recent achievements

Author keywords

[No Author keywords available]

Indexed keywords

CELL NUCLEUS DNA; GENE PRODUCT; MITOCHONDRIAL DNA; SUCCINATE DEHYDROGENASE (UBIQUINONE);

EID: 0035684666     PISSN: 13507540     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019052-200112000-00016     Document Type: Review
Times cited : (23)

References (54)
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  • 14
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    • Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain
    • (1998) Genomics , vol.54 , pp. 494-504
    • Petruzzella, V.1    Tiranti, V.2    Fernandez, P.3
  • 15
    • 17944381521 scopus 로고    scopus 로고
    • A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure
    • (2001) Nat Genet , vol.29 , pp. 57-60
    • De Lonlay, P.1    Valnot, I.2    Barrientos, A.3
  • 16
    • 0034327415 scopus 로고    scopus 로고
    • A novel frameshift mutation of the mtDNA COIII gene reads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome
    • (2000) Hum Mol Genet , vol.9 , pp. 2733-2742
    • Tiranti, V.1    Corona, P.2    Greco, M.3
  • 17
    • 0031788095 scopus 로고    scopus 로고
    • A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser) (UCN) mutations in a subgroup with syndromal encephalopathy
    • (1998) J Med Genet , vol.35 , pp. 895-900
    • Jaksch, M.1    Hofmann, S.2    Kleinle, S.3
  • 20
    • 17344362021 scopus 로고    scopus 로고
    • SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
    • (1998) Nat Genet , vol.20 , pp. 337-343
    • Zhu, Z.1    Yao, J.2    Johns, T.3
  • 36
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    • Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency
    • (1999) Hum Mol Genet , vol.8 , pp. 2541-2549
    • Yao, J.1    Shoubridge, E.A.2
  • 52
    • 0035102548 scopus 로고    scopus 로고
    • The mitochondrial inner membrane protein Lpe 10p, a homologue of Mrs2p, is essential for magnesium homeostasis and group II intron splicing in yeast
    • (2001) Mol Gen Genet , vol.264 , pp. 773-781
    • Gregan, J.1    Bui, D.M.2    Pillich, R.3
  • 54
    • 0033772263 scopus 로고    scopus 로고
    • Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
    • (2000) Nat Genet , vol.26 , pp. 176-181
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.