These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 1962049)

  • 1. The molecular pathology of human respiratory chain defects.
    Morgan-Hughes JA; Cooper JM; Schapira AH; Sweeny M; Holt IJ; Harding AE; Clark JB
    Rev Neurol (Paris); 1991; 147(6-7):450-4. PubMed ID: 1962049
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.
    Holt IJ; Harding AE; Morgan-Hughes JA
    Nature; 1988 Feb; 331(6158):717-9. PubMed ID: 2830540
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial encephalomyopathies: biochemical approach.
    Dimauro S; Moraes CT; Shanske S; Lombes A; Nakase H; Mita S; Tritschler HJ; Bonilla E; Miranda AF; Schon EA
    Rev Neurol (Paris); 1991; 147(6-7):443-9. PubMed ID: 1660180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.
    Holt IJ; Harding AE; Cooper JM; Schapira AH; Toscano A; Clark JB; Morgan-Hughes JA
    Ann Neurol; 1989 Dec; 26(6):699-708. PubMed ID: 2604380
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathies.
    Morgan-Hughes JA; Schapira AH; Cooper JM; Holt IJ; Harding AE; Clark JB
    Biochim Biophys Acta; 1990 Jul; 1018(2-3):217-22. PubMed ID: 2168209
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy].
    Marsac C; Degoul F; Bonne G; Romero N; Nelson I; Fardeau M; François D; Ponsot G; Harpey JP; Eymard B
    Rev Neurol (Paris); 1991; 147(6-7):462-6. PubMed ID: 1962051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Age-dependent respiratory function decline and DNA deletions in human muscle mitochondria.
    Hsieh RH; Hou JH; Hsu HS; Wei YH
    Biochem Mol Biol Int; 1994 Apr; 32(6):1009-22. PubMed ID: 8061617
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
    Zeviani M; Servidei S; Gellera C; Bertini E; DiMauro S; DiDonato S
    Nature; 1989 May; 339(6222):309-11. PubMed ID: 2725645
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nuclear gene defects in respiratory chain disorders.
    Shoubridge EA
    Semin Neurol; 2001 Sep; 21(3):261-7. PubMed ID: 11641816
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complete sequence of the mitochondrial genome of Tetrahymena pyriformis and comparison with Paramecium aurelia mitochondrial DNA.
    Burger G; Zhu Y; Littlejohn TG; Greenwood SJ; Schnare MN; Lang BF; Gray MW
    J Mol Biol; 2000 Mar; 297(2):365-80. PubMed ID: 10715207
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial myopathies.
    DiMauro S; Bonilla E; Zeviani M; Nakagawa M; DeVivo DC
    Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial abnormalities in inclusion-body myositis.
    Oldfors A; Moslemi AR; Jonasson L; Ohlsson M; Kollberg G; Lindberg C
    Neurology; 2006 Jan; 66(2 Suppl 1):S49-55. PubMed ID: 16432145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Expression of a defect in the respiratory chain in cultured human cells].
    Meola G; Rotondo G; Velicogna M; Toppi R; Sansone V; Bresolin N; Comi G; Bordoni A; Amati P; Ausenda C
    Riv Neurol; 1991; 61(4):122-34. PubMed ID: 1667713
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Molecular studies in Cuban patients with progressive external ophthalmoplegia].
    Rodríguez-Hernández M; Hirano M; Arrieta T; Lestayo Z; Estrada R; Santiesteban R; Guerra-Badía R; Galarraga J; Gutierres J; Hechevarría E; Andreu A; Montoya J; DiMauro S
    Rev Neurol; 2000 Jun 1-15; 30(11):1001-5. PubMed ID: 10904941
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial abnormalities in myofibrillar myopathies.
    Joshi PR; Hauburger A; Kley R; Claeys KG; Schneider I; Kress W; Stoltenburg G; Weis J; Vorgerd M; Deschauer M; Hanisch F
    Clin Neuropathol; 2014; 33(2):134-42. PubMed ID: 24361111
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Random mtDNA deletions and functional consequence in aged human skeletal muscle.
    Chabi B; Mousson de Camaret B; Chevrollier A; Boisgard S; Stepien G
    Biochem Biophys Res Commun; 2005 Jul; 332(2):542-9. PubMed ID: 15896715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evolution of interacting proteins in the mitochondrial electron transport system in a marine copepod.
    Willett CS; Burton RS
    Mol Biol Evol; 2004 Mar; 21(3):443-53. PubMed ID: 14660687
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial diseases.
    Zeviani M; Taroni F
    Baillieres Clin Neurol; 1994 Aug; 3(2):315-34. PubMed ID: 7952850
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.