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200 related items for PubMed ID: 11160915

  • 1. Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR.
    Szuhai K, Ouweland J, Dirks R, Lemaître M, Truffert J, Janssen G, Tanke H, Holme E, Maassen J, Raap A.
    Nucleic Acids Res; 2001 Feb 01; 29(3):E13. PubMed ID: 11160915
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  • 2. [Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].
    Tanno Y, Yoneda M, Tanaka K, Tsuji S.
    Nihon Rinsho; 1993 Sep 01; 51(9):2379-85. PubMed ID: 8411716
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  • 4. Analysis of mtDNA copy number and composition of single mitochondrial particles using flow cytometry and PCR.
    Cavelier L, Johannisson A, Gyllensten U.
    Exp Cell Res; 2000 Aug 25; 259(1):79-85. PubMed ID: 10942580
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  • 7. [The correlation of the heteroplasmy of mtDNA and clinicopathological findings in the patients with mitochondrial encephalomyopathies].
    Tanno Y, Tanaka K, Tsuji S.
    Nihon Rinsho; 1997 Dec 25; 55(12):3270-6. PubMed ID: 9436449
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  • 8. Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism.
    Masucci JP, Schon EA, King MP.
    Mol Cell Biochem; 1997 Sep 25; 174(1-2):215-9. PubMed ID: 9309690
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  • 10. [Clinical heterogeneity associated with mitochondrial DNA A8344G point mutation].
    Zhao J, Zhao DH, Zhang W, Lü H, Yuan Y, Qi Y, Wang ZX.
    Zhonghua Yi Xue Za Zhi; 2012 Oct 30; 92(40):2835-8. PubMed ID: 23290212
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  • 11. Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation.
    Chen CY, Chen HF, Gi SJ, Chi TH, Cheng CK, Hsu CF, Ma YS, Wei YH, Liu CS, Hsieh M.
    Mitochondrion; 2011 Sep 30; 11(5):739-49. PubMed ID: 21679777
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  • 13. Regionalized pathology correlates with augmentation of mtDNA copy numbers in a patient with myoclonic epilepsy with ragged-red fibers (MERRF-syndrome).
    Brinckmann A, Weiss C, Wilbert F, von Moers A, Zwirner A, Stoltenburg-Didinger G, Wilichowski E, Schuelke M.
    PLoS One; 2010 Oct 20; 5(10):e13513. PubMed ID: 20976001
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  • 16. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
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  • 17. The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation.
    Chen HF, Chen CY, Lin TH, Huang ZW, Chi TH, Ma YS, Wu SB, Wei YH, Hsieh M.
    FEBS J; 2012 Aug 15; 279(16):2987-3001. PubMed ID: 22742457
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  • 18. The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.
    Hammans SR, Sweeney MG, Brockington M, Lennox GG, Lawton NF, Kennedy CR, Morgan-Hughes JA, Harding AE.
    Brain; 1993 Jun 15; 116 ( Pt 3)():617-32. PubMed ID: 8513395
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