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Journal Abstract Search

129 related items for PubMed ID: 11935339

  • 21. Identification of a novel T398A mutation in the ND5 subunit of the mitochondrial complex I and of three novel mtDNA polymorphisms in two patients presenting ocular symptoms.
    Batandier C, Picard A, Tessier N, Lunardi J.
    Hum Mutat; 2000 Dec; 16(6):532. PubMed ID: 11102991
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  • 22. Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma.
    Gasparre G, Hervouet E, de Laplanche E, Demont J, Pennisi LF, Colombel M, Mège-Lechevallier F, Scoazec JY, Bonora E, Smeets R, Smeitink J, Lazar V, Lespinasse J, Giraud S, Godinot C, Romeo G, Simonnet H.
    Hum Mol Genet; 2008 Apr 01; 17(7):986-95. PubMed ID: 18156159
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  • 23. Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families.
    Iida A, Saito S, Sekine A, Kitamoto T, Kitamura Y, Mishima C, Osawa S, Kondo K, Harigae S, Nakamura Y.
    J Hum Genet; 2001 Apr 01; 46(7):385-407. PubMed ID: 11450848
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  • 24. cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.
    Loeffen JL, Triepels RH, van den Heuvel LP, Schuelke M, Buskens CA, Smeets RJ, Trijbels JM, Smeitink JA.
    Biochem Biophys Res Commun; 1998 Dec 18; 253(2):415-22. PubMed ID: 9878551
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  • 25. Biogenesis of respiratory complex I.
    Schulte U.
    J Bioenerg Biomembr; 2001 Jun 18; 33(3):205-12. PubMed ID: 11695830
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  • 32. Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy.
    Musumeci O, Andreu AL, Shanske S, Bresolin N, Comi GP, Rothstein R, Schon EA, DiMauro S.
    Am J Hum Genet; 2000 Jun 18; 66(6):1900-4. PubMed ID: 10775530
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  • 33. Functional sulfurtransferase is associated with mitochondrial complex I from Yarrowia lipolytica, but is not required for assembly of its iron-sulfur clusters.
    Abdrakhmanova A, Dobrynin K, Zwicker K, Kerscher S, Brandt U.
    FEBS Lett; 2005 Dec 19; 579(30):6781-5. PubMed ID: 16310785
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  • 34. Characterization of the NADH:ubiquinone oxidoreductase (complex I) in the trypanosomatid Phytomonas serpens (Kinetoplastida).
    Cermáková P, Verner Z, Man P, Lukes J, Horváth A.
    FEBS J; 2007 Jun 19; 274(12):3150-8. PubMed ID: 17521330
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  • 35. hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assembly.
    Sacconi S, Trevisson E, Pistollato F, Baldoin MC, Rezzonico R, Bourget I, Desnuelle C, Tenconi R, Basso G, DiMauro S, Salviati L.
    Biochem Biophys Res Commun; 2005 Nov 25; 337(3):832-9. PubMed ID: 16212937
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  • 36. Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J.
    Moilanen JS, Finnila S, Majamaa K.
    Mol Biol Evol; 2003 Dec 25; 20(12):2132-42. PubMed ID: 12949126
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  • 37. Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.
    Mancuso M, Filosto M, Bonilla E, Hirano M, Shanske S, Vu TH, DiMauro S.
    Arch Neurol; 2003 Jul 25; 60(7):1007-9. PubMed ID: 12873860
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  • 38. Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.
    Mayr JA, Meierhofer D, Zimmermann F, Feichtinger R, Kögler C, Ratschek M, Schmeller N, Sperl W, Kofler B.
    Clin Cancer Res; 2008 Apr 15; 14(8):2270-5. PubMed ID: 18413815
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  • 39. Sequence homology of NADH CoQ reductase subunit IV with nucleotide-requiring enzymes.
    Isashiki Y, Ohba N, Uto M, Nakagawa M.
    Jpn J Ophthalmol; 1993 Apr 15; 37(1):39-42. PubMed ID: 8320863
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