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PUBMED FOR HANDHELDS

Journal Abstract Search


171 related items for PubMed ID: 9860297

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  • 2. cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completed.
    Loeffen J, van den Heuvel L, Smeets R, Triepels R, Sengers R, Trijbels F, Smeitink J.
    Biochem Biophys Res Commun; 1998 Jun 29; 247(3):751-8. PubMed ID: 9647766
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  • 3. The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients.
    Loeffen J, Smeets R, Smeitink J, Triepels R, Sengers R, Trijbels F, van den Heuvel L.
    J Inherit Metab Dis; 1999 Feb 29; 22(1):19-28. PubMed ID: 10070614
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  • 4. Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I.
    Smeitink J, Loeffen J, Smeets R, Triepels R, Ruitenbeek W, Trijbels F, van den Heuvel L.
    Hum Genet; 1998 Aug 29; 103(2):245-50. PubMed ID: 9760212
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  • 7. cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I.
    Procaccio V, Depetris D, Soularue P, Mattei MG, Lunardi J, Issartel JP.
    Biochim Biophys Acta; 1997 Mar 20; 1351(1-2):37-41. PubMed ID: 9116042
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  • 8. Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene.
    de Coo R, Buddiger P, Smeets H, Geurts van Kessel A, Morgan-Hughes J, Weghuis DO, Overhauser J, van Oost B.
    Genomics; 1995 Apr 10; 26(3):461-6. PubMed ID: 7607668
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  • 9. Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunit.
    Kim JW, Lee Y, Kang HB, Chose YK, Chung TW, Chang SY, Lee KS, Choe IS.
    Biochem Mol Biol Int; 1997 Oct 10; 43(3):669-75. PubMed ID: 9352085
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  • 10. Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency.
    Bénit P, Chretien D, Kadhom N, de Lonlay-Debeney P, Cormier-Daire V, Cabral A, Peudenier S, Rustin P, Munnich A, Rötig A.
    Am J Hum Genet; 2001 Jun 10; 68(6):1344-52. PubMed ID: 11349233
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  • 11. A human cDNA encoding the homologue of NADH: ubiquinone oxidoreductase subunit B13.
    Pata I, Tensing K, Metspalu A.
    Biochim Biophys Acta; 1997 Feb 07; 1350(2):115-8. PubMed ID: 9048877
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  • 12. Anoxia-induced gene expression in turtle heart. Upregulation of mitochondrial genes for NADH-ubiquinone oxidoreductase subunit 5 and cytochrome c oxidase subunit 1.
    Cai Q, Storey KB.
    Eur J Biochem; 1996 Oct 01; 241(1):83-92. PubMed ID: 8898892
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  • 17. Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13.
    Hyslop SJ, Duncan AM, Pitkänen S, Robinson BH.
    Genomics; 1996 Nov 01; 37(3):375-80. PubMed ID: 8938450
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  • 19. Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15.
    Russell MW, du Manoir S, Collins FS, Brody LC.
    Mamm Genome; 1997 Jan 01; 8(1):60-1. PubMed ID: 9021153
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