BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 8506008)

  • 21. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features.
    Thyagarajan D; Byrne E
    Int Rev Neurobiol; 2002; 53():93-144. PubMed ID: 12512338
    [No Abstract]   [Full Text] [Related]  

  • 22. An evaluation of the measurement of the activities of complexes I-IV in the respiratory chain of human skeletal muscle mitochondria.
    Birch-Machin MA; Briggs HL; Saborido AA; Bindoff LA; Turnbull DM
    Biochem Med Metab Biol; 1994 Feb; 51(1):35-42. PubMed ID: 8192914
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mitochondrial DNA in Parkinson's disease.
    Schapira AH
    Adv Neurol; 1999; 80():233-7. PubMed ID: 10410727
    [No Abstract]   [Full Text] [Related]  

  • 24. Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene.
    Birch-Machin MA; Taylor RW; Cochran B; Ackrell BA; Turnbull DM
    Ann Neurol; 2000 Sep; 48(3):330-5. PubMed ID: 10976639
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mitochondrial complex I deficiency in Parkinson's disease.
    Schapira AH
    Adv Neurol; 1993; 60():288-91. PubMed ID: 8420145
    [No Abstract]   [Full Text] [Related]  

  • 26. [Ptosis and asthenia manifesting a mitochondrial myopathy].
    Disdier P; Harlé JR; Figarella-Branger D; Chérif AA; Desnuelle C; Weiller PJ
    Rev Med Interne; 1992; 13(5):381-3. PubMed ID: 1344837
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comparative study and cDNA cloning of the flavoprotein subunit of mitochondrial complex II (succinate-ubiquinone oxidoreductase: fumarate reductase) from the dog heartworm, Dirofilaria immitis.
    Kuramochi T; Kita K; Takamiya S; Kojima S; Hayasaki M
    Comp Biochem Physiol B Biochem Mol Biol; 1995 Jul; 111(3):491-502. PubMed ID: 7613771
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Platelet mitochondrial DNA in Parkinson's disease.
    Schapira AH; Marsden CD
    Mov Disord; 1994 Jan; 9(1):119-21. PubMed ID: 8139599
    [No Abstract]   [Full Text] [Related]  

  • 29. Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.
    Angelini C; Melacini P; Valente ML; Reichmann H; Carrozzo R; Fanin M; Vergani L; Boffa GM; Martinuzzi A; Fasoli G
    Jpn Heart J; 1993 Jan; 34(1):63-77. PubMed ID: 8515573
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Succinate: quinone oxidoreductases. Variations on a conserved theme.
    Hägerhäll C
    Biochim Biophys Acta; 1997 Jun; 1320(2):107-41. PubMed ID: 9210286
    [No Abstract]   [Full Text] [Related]  

  • 31. [Electron transfer complex II deficiency].
    Goto Y
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):491-3. PubMed ID: 9645117
    [No Abstract]   [Full Text] [Related]  

  • 32. Deficiencies of NADH and succinate dehydrogenases in degenerative diseases and myopathies.
    Singer TP; Ramsay RR; Ackrell BA
    Biochim Biophys Acta; 1995 May; 1271(1):211-9. PubMed ID: 7599211
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gene of the month.
    Nat Biotechnol; 1996 Dec; 14(13):1638. PubMed ID: 9634834
    [No Abstract]   [Full Text] [Related]  

  • 34. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
    Taschner PE; Bröcker-Vriends AH; van der Mey AG
    Ned Tijdschr Geneeskd; 2002 Nov; 146(46):2188-90. PubMed ID: 12467161
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mitochondrial mutations differentially affect aging, mutability and anesthetic sensitivity in Caenorhabditis elegans.
    Hartman PS; Ishii N; Kayser EB; Morgan PG; Sedensky MM
    Mech Ageing Dev; 2001 Aug; 122(11):1187-201. PubMed ID: 11389932
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. [Mitochondrial disease].
    Goto Y
    Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):496-502. PubMed ID: 11032007
    [No Abstract]   [Full Text] [Related]  

  • 38. [Mitochondriopathies].
    Ricoy-Campo JR; Cabello A
    Rev Neurol; 2003 Oct 16-31; 37(8):775-9. PubMed ID: 14593640
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The electron transport chain in anaerobically functioning eukaryotes.
    Tielens AG; Van Hellemond JJ
    Biochim Biophys Acta; 1998 Jun; 1365(1-2):71-8. PubMed ID: 9693724
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy.
    Saada A; Shaag A; Mandel H; Nevo Y; Eriksson S; Elpeleg O
    Nat Genet; 2001 Nov; 29(3):342-4. PubMed ID: 11687801
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.