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Journal Abstract Search

132 related items for PubMed ID: 15965045

  • 1. Upregulation of matrix metalloproteinase 1 and disruption of mitochondrial network in skin fibroblasts of patients with MERRF syndrome.
    Ma YS, Chen YC, Lu CY, Liu CY, Wei YH.
    Ann N Y Acad Sci; 2005 May; 1042():55-63. PubMed ID: 15965045
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  • 2. Involvement of protein kinase C delta in the alteration of mitochondrial mass in human cells under oxidative stress.
    Lee CF, Chen YC, Liu CY, Wei YH.
    Free Radic Biol Med; 2006 Jun 15; 40(12):2136-46. PubMed ID: 16785027
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  • 3. Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 nt.
    Antonická H, Floryk D, Klement P, Stratilová L, Hermanská J, Houstková H, Kalous M, Drahota Z, Zeman J, Houstek J.
    Biochem J; 1999 Sep 15; 342 Pt 3(Pt 3):537-44. PubMed ID: 10477264
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  • 4. Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome.
    Wu SB, Ma YS, Wu YT, Chen YC, Wei YH.
    Mol Neurobiol; 2010 Jun 15; 41(2-3):256-66. PubMed ID: 20411357
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  • 5. Overexpression of matrix metalloproteinase 1 in dermal fibroblasts from DNA repair-deficient/cancer-prone xeroderma pigmentosum group C patients.
    Fréchet M, Warrick E, Vioux C, Chevallier O, Spatz A, Benhamou S, Sarasin A, Bernerd F, Magnaldo T.
    Oncogene; 2008 Sep 04; 27(39):5223-32. PubMed ID: 18469853
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  • 6. Fibrous dysplasia in a child with mitochondrial A8344G mutation.
    Chen ST, Fan PC, Hwu WL, Wu MH.
    J Child Neurol; 2008 Dec 04; 23(12):1447-50. PubMed ID: 18772492
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  • 8. Treatment of human cells derived from MERRF syndrome by peptide-mediated mitochondrial delivery.
    Chang JC, Liu KH, Chuang CS, Su HL, Wei YH, Kuo SJ, Liu CS.
    Cytotherapy; 2013 Dec 04; 15(12):1580-96. PubMed ID: 24199594
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  • 10. 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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  • 12. Unusual presentations of patients with the mitochondrial MERRF mutation A8344G.
    Wiedemann FR, Bartels C, Kirches E, Mawrin C, Wallesch CW.
    Clin Neurol Neurosurg; 2008 Sep 15; 110(8):859-63. PubMed ID: 18657354
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  • 13. Parkin-mediated mitophagy and autophagy flux disruption in cellular models of MERRF syndrome.
    Villanueva-Paz M, Povea-Cabello S, Villalón-García I, Álvarez-Córdoba M, Suárez-Rivero JM, Talaverón-Rey M, Jackson S, Falcón-Moya R, Rodríguez-Moreno A, Sánchez-Alcázar JA.
    Biochim Biophys Acta Mol Basis Dis; 2020 Jun 01; 1866(6):165726. PubMed ID: 32061767
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  • 15. Oxidative stress-induced c-Jun N-terminal kinase (JNK) activation in tendon cells upregulates MMP1 mRNA and protein expression.
    Wang F, Murrell GA, Wang MX.
    J Orthop Res; 2007 Mar 01; 25(3):378-89. PubMed ID: 17106880
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  • 17. Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case report.
    Sitburana O, Witoonpanich R, Phudhichareonrat S, Lertrit P, Supavilai R.
    J Med Assoc Thai; 2001 Jul 01; 84(7):1051-5. PubMed ID: 11759966
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  • 20. Genetic analysis of one family with myoclonic epilepsy and ragged-red fibers (MERRF).
    Campos Y, Esteban J, Cabello A, Arenas J.
    Muscle Nerve; 1994 Oct 01; 17(10):1229-31. PubMed ID: 7935536
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