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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

101 related items for PubMed ID: 9545512

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  • 7. Cytochrome c oxidase-deficient patients have distinct subunit assembly profiles.
    Hanson BJ, Carrozzo R, Piemonte F, Tessa A, Robinson BH, Capaldi RA.
    J Biol Chem; 2001 May 11; 276(19):16296-301. PubMed ID: 11278850
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  • 9. Human cytochrome oxidase deficiency.
    Robinson BH.
    Pediatr Res; 2000 Nov 11; 48(5):581-5. PubMed ID: 11044474
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  • 11. LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.
    Debray FG, Morin C, Janvier A, Villeneuve J, Maranda B, Laframboise R, Lacroix J, Decarie JC, Robitaille Y, Lambert M, Robinson BH, Mitchell GA.
    J Med Genet; 2011 Mar 11; 48(3):183-9. PubMed ID: 21266382
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  • 15. Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome.
    Weraarpachai W, Antonicka H, Sasarman F, Seeger J, Schrank B, Kolesar JE, Lochmüller H, Chevrette M, Kaufman BA, Horvath R, Shoubridge EA.
    Nat Genet; 2009 Jul 11; 41(7):833-7. PubMed ID: 19503089
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  • 18. Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle.
    Bachman NJ, Riggs PK, Siddiqui N, Makris GJ, Womack JE, Lomax MI.
    Genomics; 1997 May 15; 42(1):146-51. PubMed ID: 9177785
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  • 19. 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
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