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Journal Abstract Search

232 related items for PubMed ID: 14995902

  • 1. Genetic defects in the oxidative phosphorylation (OXPHOS) system.
    Janssen RJ, van den Heuvel LP, Smeitink JA.
    Expert Rev Mol Diagn; 2004 Mar; 4(2):143-56. PubMed ID: 14995902
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  • 2. The genetics and pathology of oxidative phosphorylation.
    Smeitink J, van den Heuvel L, DiMauro S.
    Nat Rev Genet; 2001 May; 2(5):342-52. PubMed ID: 11331900
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  • 4. The transmission of OXPHOS disease and methods to prevent this.
    Jacobs LJ, de Wert G, Geraedts JP, de Coo IF, Smeets HJ.
    Hum Reprod Update; 2006 May; 12(2):119-36. PubMed ID: 16199488
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  • 5. Mitochondrial medicine--molecular pathology of defective oxidative phosphorylation.
    Fosslien E.
    Ann Clin Lab Sci; 2001 Jan; 31(1):25-67. PubMed ID: 11314862
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  • 7. [Enzyme complex defects of the mitochondrial respiratory chain].
    Rubio JC, Martín MA, del Hoyo P, de Bustos F, Campos Y, Arenas J.
    Rev Neurol; 1998 Apr; 26 Suppl 1():S15-20. PubMed ID: 9810586
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  • 8. Respiratory mutations lead to different pleiotropic effects on OXPHOS complexes in yeast and in human cells.
    Marsy S, Frachon P, Dujardin G, Lombès A, Lemaire C.
    FEBS Lett; 2008 Oct 15; 582(23-24):3489-93. PubMed ID: 18804471
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  • 12. [Mitochondrial disorders: a classification for the 21st century].
    Andreu AL, Gonzalo-Sanz R.
    Neurologia; 2004 Oct 15; 19(1):15-22. PubMed ID: 14762729
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  • 13. [Diseases of mitochondrial DNA].
    Montoya J, Playán A, Solano A, Alcaine MJ, López-Pérez MJ, Pérez-Martos A.
    Rev Neurol; 2004 Oct 15; 31(4):324-33. PubMed ID: 11008288
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  • 14. Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects.
    Fernández-Vizarra E, Tiranti V, Zeviani M.
    Biochim Biophys Acta; 2009 Jan 15; 1793(1):200-11. PubMed ID: 18620006
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  • 16. Oxidative phosphorylation diseases and cerebellar ataxia.
    Shoffner JM, Kaufman A, Koontz D, Krawiecki N, Smith E, Topp M, Wallace DC.
    Clin Neurosci; 1995 Jan 15; 3(1):43-53. PubMed ID: 7614094
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  • 17. A genome-wide shRNA screen for new OxPhos related genes.
    Bayona-Bafaluy MP, Sánchez-Cabo F, Fernández-Silva P, Pérez-Martos A, Enríquez JA.
    Mitochondrion; 2011 May 15; 11(3):467-75. PubMed ID: 21292037
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  • 18. Are Escherichia coli OXPHOS complexes concentrated in specialized zones within the plasma membrane?
    Lenn T, Leake MC, Mullineaux CW.
    Biochem Soc Trans; 2008 Oct 15; 36(Pt 5):1032-6. PubMed ID: 18793184
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  • 19. Mitochondrial oxidative phosphorylation defects in Parkinson's disease.
    Shoffner JM, Watts RL, Juncos JL, Torroni A, Wallace DC.
    Ann Neurol; 1991 Sep 15; 30(3):332-9. PubMed ID: 1952821
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  • 20. Mitochondrial complex I is deficient in renal oncocytomas.
    Simonnet H, Demont J, Pfeiffer K, Guenaneche L, Bouvier R, Brandt U, Schagger H, Godinot C.
    Carcinogenesis; 2003 Sep 15; 24(9):1461-6. PubMed ID: 12844484
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