BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 11803021)

  • 1. Inborn errors of complex II--unusual human mitochondrial diseases.
    Rustin P; Rötig A
    Biochim Biophys Acta; 2002 Jan; 1553(1-2):117-22. PubMed ID: 11803021
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotypic dichotomy in mitochondrial complex II genetic disorders.
    Baysal BE; Rubinstein WS; Taschner PE
    J Mol Med (Berl); 2001 Sep; 79(9):495-503. PubMed ID: 11692162
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Succinate dehydrogenase deficiency in human.
    Brière JJ; Favier J; El Ghouzzi V; Djouadi F; Bénit P; Gimenez AP; Rustin P
    Cell Mol Life Sci; 2005 Oct; 62(19-20):2317-24. PubMed ID: 16143825
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial myopathies.
    DiMauro S; Bonilla E; Zeviani M; Servidei S; DeVivo DC; Schon EA
    J Inherit Metab Dis; 1987; 10 Suppl 1():113-28. PubMed ID: 2824920
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Complex II (succinate-ubiquinone reductase) deficiency].
    Nonaka I
    Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
    [No Abstract]   [Full Text] [Related]  

  • 6. Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.
    Birch-Machin MA; Marsac C; Ponsot G; Parfait B; Taylor RW; Rustin P; Munnich A
    Biochem Biophys Res Commun; 1996 Mar; 220(1):57-62. PubMed ID: 8602857
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Optic atrophy and ataxia (complex II deficiency-mutation in Fp subunit gene of succinate dehydrogenase)].
    Goto Y
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():376-7. PubMed ID: 12013890
    [No Abstract]   [Full Text] [Related]  

  • 8. Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency.
    Alston CL; Davison JE; Meloni F; van der Westhuizen FH; He L; Hornig-Do HT; Peet AC; Gissen P; Goffrini P; Ferrero I; Wassmer E; McFarland R; Taylor RW
    J Med Genet; 2012 Sep; 49(9):569-77. PubMed ID: 22972948
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The genetic basis of isolated mitochondrial complex II deficiency.
    Fullerton M; McFarland R; Taylor RW; Alston CL
    Mol Genet Metab; 2020; 131(1-2):53-65. PubMed ID: 33162331
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Succinate: quinone oxidoreductases: new insights from X-ray crystal structures.
    Lancaster CR; Kröger A
    Biochim Biophys Acta; 2000 Aug; 1459(2-3):422-31. PubMed ID: 11004459
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Complex II deficiency due to Fp gene mutation].
    Ito M
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():444-5. PubMed ID: 12013908
    [No Abstract]   [Full Text] [Related]  

  • 12. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
    Niemann S; Müller U
    Nat Genet; 2000 Nov; 26(3):268-70. PubMed ID: 11062460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Succinate dehydrogenase and human diseases: new insights into a well-known enzyme.
    Rustin P; Munnich A; Rötig A
    Eur J Hum Genet; 2002 May; 10(5):289-91. PubMed ID: 12082502
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Succinate:quinone oxidoreductases from epsilon-proteobacteria.
    Lancaster CR; Simon J
    Biochim Biophys Acta; 2002 Jan; 1553(1-2):84-101. PubMed ID: 11803019
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Cytopathies involving mitochondrial complex II.
    Ackrell BA
    Mol Aspects Med; 2002 Oct; 23(5):369-84. PubMed ID: 12231007
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human.
    Rustin P; Bourgeron T; Parfait B; Chretien D; Munnich A; Rötig A
    Biochim Biophys Acta; 1997 Aug; 1361(2):185-97. PubMed ID: 9300800
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A role for mitochondrial enzymes in inherited neoplasia and beyond.
    Eng C; Kiuru M; Fernandez MJ; Aaltonen LA
    Nat Rev Cancer; 2003 Mar; 3(3):193-202. PubMed ID: 12612654
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Architecture of succinate dehydrogenase and reactive oxygen species generation.
    Yankovskaya V; Horsefield R; Törnroth S; Luna-Chavez C; Miyoshi H; Léger C; Byrne B; Cecchini G; Iwata S
    Science; 2003 Jan; 299(5607):700-4. PubMed ID: 12560550
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.