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Journal Abstract Search

248 related items for PubMed ID: 7807166

  • 1. Expression of cytochrome c oxidase subunits encoded by mitochondrial or nuclear DNA in the muscle of patients with zidovudine myopathy.
    Chariot P, Bonne G, Authier FJ, Marsac C, Gherardi R.
    J Neurol Sci; 1994 Sep; 125(2):190-3. PubMed ID: 7807166
    [Abstract] [Full Text] [Related]

  • 2. Cytochrome c oxidase deficiency in the muscle of patients with zidovudine myopathy is segmental and affects both mitochondrial DNA- and nuclear DNA-encoded subunits.
    Yerroum M, Pham-Dang C, Authier FJ, Monnet I, Gherardi R, Chariot P.
    Acta Neuropathol; 2000 Jul; 100(1):82-6. PubMed ID: 10912924
    [Abstract] [Full Text] [Related]

  • 3. Cytochrome c oxidase deficiency in zidovudine myopathy affects perifascicular muscle fibres and arterial smooth muscle cells.
    Chariot P, Le Maguet F, Authier FJ, Labes D, Poron F, Gherardi R.
    Neuropathol Appl Neurobiol; 1995 Dec; 21(6):540-7. PubMed ID: 8745244
    [Abstract] [Full Text] [Related]

  • 4. Cytochrome c oxidase reaction improves histopathological assessment of zidovudine myopathy.
    Chariot P, Monnet I, Gherardi R.
    Ann Neurol; 1993 Oct; 34(4):561-5. PubMed ID: 8215243
    [Abstract] [Full Text] [Related]

  • 5. HIV or zidovudine myopathy?
    Gherardi R, Chariot P.
    Neurology; 1994 Feb; 44(2):361-2; author reply 362-4. PubMed ID: 8309597
    [No Abstract] [Full Text] [Related]

  • 6. Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.
    Goto Y, Koga Y, Horai S, Nonaka I.
    J Neurol Sci; 1990 Dec; 100(1-2):63-9. PubMed ID: 1965208
    [Abstract] [Full Text] [Related]

  • 7. Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia.
    Taanman JW, Burton MD, Marusich MF, Kennaway NG, Capaldi RA.
    Biochim Biophys Acta; 1996 Apr 12; 1315(3):199-207. PubMed ID: 8611660
    [Abstract] [Full Text] [Related]

  • 8. AZT-induced mitochondrial myopathy.
    Tomelleri G, Tonin P, Spadaro M, Tilia G, Orrico D, Barelli A, Bonetti B, Monaco S, Salviati A, Morocutti C.
    Ital J Neurol Sci; 1992 Dec 12; 13(9):723-8. PubMed ID: 1336487
    [Abstract] [Full Text] [Related]

  • 9. Major growth reduction and minor decrease in mitochondrial enzyme activity in cultured human muscle cells after exposure to zidovudine.
    Herzberg NH, Zorn I, Zwart R, Portegies P, Bolhuis PA.
    Muscle Nerve; 1992 Jun 12; 15(6):706-10. PubMed ID: 1324428
    [Abstract] [Full Text] [Related]

  • 10. Partial cytochrome c oxidase deficiency and cytoplasmic bodies in patients with zidovudine myopathy.
    Chariot P, Gherardi R.
    Neuromuscul Disord; 1991 Jun 12; 1(5):357-63. PubMed ID: 1668320
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial DNA deletions in muscle fibers in inclusion body myositis.
    Oldfors A, Moslemi AR, Fyhr IM, Holme E, Larsson NG, Lindberg C.
    J Neuropathol Exp Neurol; 1995 Jul 12; 54(4):581-7. PubMed ID: 7602331
    [Abstract] [Full Text] [Related]

  • 12. Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.
    Prelle A, Moggio M, Checcarelli N, Comi G, Bresolin N, Battistel A, Bordoni A, Scarlato G.
    J Neurol Sci; 1993 Jul 12; 117(1-2):24-7. PubMed ID: 8410061
    [Abstract] [Full Text] [Related]

  • 13. Uridine supplementation antagonizes zidovudine-induced mitochondrial myopathy and hyperlactatemia in mice.
    Lebrecht D, Deveaud C, Beauvoit B, Bonnet J, Kirschner J, Walker UA.
    Arthritis Rheum; 2008 Jan 12; 58(1):318-26. PubMed ID: 18163507
    [Abstract] [Full Text] [Related]

  • 14. Mitochondria in cultured human muscle cells depleted of mitochondrial DNA.
    Herzberg NH, Middelkoop E, Adorf M, Dekker HL, Van Galen MJ, Van den Berg M, Bolhuis PA, Van den Bogert C.
    Eur J Cell Biol; 1993 Aug 12; 61(2):400-8. PubMed ID: 8223726
    [Abstract] [Full Text] [Related]

  • 15. Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy.
    Sciacco M, Bonilla E, Schon EA, DiMauro S, Moraes CT.
    Hum Mol Genet; 1994 Jan 12; 3(1):13-9. PubMed ID: 8162014
    [Abstract] [Full Text] [Related]

  • 16. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M.
    J Neurol Sci; 1992 Jul 12; 110(1-2):169-77. PubMed ID: 1324295
    [Abstract] [Full Text] [Related]

  • 17. Structural organization and transcription regulation of nuclear genes encoding the mammalian cytochrome c oxidase complex.
    Lenka N, Vijayasarathy C, Mullick J, Avadhani NG.
    Prog Nucleic Acid Res Mol Biol; 1998 Jul 12; 61():309-44. PubMed ID: 9752724
    [Abstract] [Full Text] [Related]

  • 18. A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy.
    Rahman S, Taanman JW, Cooper JM, Nelson I, Hargreaves I, Meunier B, Hanna MG, García JJ, Capaldi RA, Lake BD, Leonard JV, Schapira AH.
    Am J Hum Genet; 1999 Oct 12; 65(4):1030-9. PubMed ID: 10486321
    [Abstract] [Full Text] [Related]

  • 19. Tubular aggregates and partial cytochrome c oxidase deficiency in skeletal muscle of patients with AIDS treated with zidovudine.
    Chariot P, Benbrik E, Schaeffer A, Gherardi R.
    Acta Neuropathol; 1993 Oct 12; 85(4):431-6. PubMed ID: 8386898
    [Abstract] [Full Text] [Related]

  • 20. Age-related decline of the cytochrome c oxidase subunit expression in the auditory cortex of the mimetic aging rat model associated with the common deletion.
    Zhong Y, Hu Y, Peng W, Sun Y, Yang Y, Zhao X, Huang X, Zhang H, Kong W.
    Hear Res; 2012 Dec 12; 294(1-2):40-8. PubMed ID: 23022596
    [Abstract] [Full Text] [Related]

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