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Neurological Sciences
Volumn 21, Issue 3 SUPPL., 2000, Pages
A novel mtDNA mutation in the ATPaseG gene studied by E. Coli modeling
Author keywords

Atp synthesis; Leigh syndrome; mtDNA
Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; MITOCHONDRIAL DNA;
EID: 0034570211     PISSN: 15901874     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)
References (7)
  • 1
    • 0030898875 scopus 로고    scopus 로고
    • 0-ATP synthases: Glimpses of interacting parts in a dynamic molecular machine
    • 0-ATP synthases: glimpses of interacting parts in a dynamic molecular machine. J Exp Biol 200:217-224
    • (1997) J Exp Biol , vol.200 , pp. 217-224
    • Fillingame, R.H.1
  • 2
    • 0029891215 scopus 로고    scopus 로고
    • Genetic heterogeneity in Leigh syndrome
    • DiMauro S, De Vivo DC (1996) Genetic heterogeneity in Leigh syndrome. Ann Neurol 40:5-7
    • (1996) Ann Neurol , vol.40 , pp. 5-7
    • Dimauro, S.1    De Vivo, D.C.2
  • 3
    • 0027336812 scopus 로고
    • The aleu207→arg mutation in F1F0-ATP synthase from Escherichia cou. a model for human mitochondrial disease
    • Hartzog PE, Cain BD (1993) The aleu207→arg mutation in F1F0-ATP synthase from Escherichia cou. A model for human mitochondrial disease. J Biol Chem 268:12250-12252
    • (1993) J Biol Chem , vol.268 , pp. 12250-12252
    • Hartzog, P.E.1    Cain, B.D.2
  • 4
    • 0027936218 scopus 로고
    • Cytoplasmic transfer of the mtDNA nt 8993 T→G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio
    • Trounce I, Neill S, Wallace DC (1994) Cytoplasmic transfer of the mtDNA nt 8993 T→G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio. Proc Natl Acad Sci USA 91:8334-8338
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 8334-8338
    • Trounce, I.1    Neill, S.2    Wallace, D.C.3
  • 5
    • 0029919608 scopus 로고    scopus 로고
    • Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome
    • Vazquez-Memije ME, Shanske S, Santorelli FM et al (1996) Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome. J Inherit Metab Dis 19:43-50
    • (1996) J Inherit Metab Dis , vol.19 , pp. 43-50
    • Vazquez-Memije, M.E.1    Shanske, S.2    Santorelli, F.M.3
  • 6
    • 0034672534 scopus 로고    scopus 로고
    • The T9176G mutation of human mtDNA gives a fully assembled but nonfunctional FIFO when modeled in E. coli
    • Carrozzo R, Murray J, Santorelli FM, Capaldi RA (2000) The T9176G mutation of human mtDNA gives a fully assembled but nonfunctional FIFO when modeled in E. coli. FEBS Lett 86:297-299
    • (2000) FEBS Lett , vol.86 , pp. 297-299
    • Carrozzo, R.1    Murray, J.2    Santorelli, F.M.3    Capaldi, R.A.4
  • 7
    • 0033971704 scopus 로고    scopus 로고
    • Cross-linking and electron microscopy studies of the structure and functioning of the Escherichia coli ATP synthase
    • Capaldi RA, Schulenberg B, Murray J, Ageller R (2000) Cross-linking and electron microscopy studies of the structure and functioning of the Escherichia coli ATP synthase. J Exp Biol 203:29-33
    • (2000) J Exp Biol , vol.203 , pp. 29-33
    • Capaldi, R.A.1    Schulenberg, B.2    Murray, J.3    Ageller, R.4

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.