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298 related items for PubMed ID: 21679777

  • 1. 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; 11(5):739-49. PubMed ID: 21679777
    [Abstract] [Full Text] [Related]

  • 2. 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; 279(16):2987-3001. PubMed ID: 22742457
    [Abstract] [Full Text] [Related]

  • 3. Effects of carbonic anhydrase-related protein VIII on human cells harbouring an A8344G mitochondrial DNA mutation.
    Wang TK, Cheng CK, Chi TH, Ma YS, Wu SB, Wei YH, Hsieh M.
    Biochem J; 2014 Apr 01; 459(1):149-60. PubMed ID: 24476000
    [Abstract] [Full Text] [Related]

  • 4. Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model.
    Lo CM, Ma YS, Wei YH, Hsieh BYT, Hsieh M.
    Arch Biochem Biophys; 2018 Mar 01; 641():50-61. PubMed ID: 29407793
    [Abstract] [Full Text] [Related]

  • 5. Hypersensitivity of A8344G MERRF mutated cybrid cells to staurosporine-induced cell death is mediated by calcium-dependent activation of calpains.
    Rommelaere G, Michel S, Malaisse J, Charlier S, Arnould T, Renard P.
    Int J Biochem Cell Biol; 2012 Jan 01; 44(1):139-49. PubMed ID: 22037425
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Recovery of MERRF fibroblasts and cybrids pathophysiology by coenzyme Q10.
    De la Mata M, Garrido-Maraver J, Cotán D, Cordero MD, Oropesa-Ávila M, Izquierdo LG, De Miguel M, Lorite JB, Infante ER, Ybot P, Jackson S, Sánchez-Alcázar JA.
    Neurotherapeutics; 2012 Apr 01; 9(2):446-63. PubMed ID: 22354625
    [Abstract] [Full Text] [Related]

  • 8. Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas.
    Larsson NG, Tulinius MH, Holme E, Oldfors A.
    Muscle Nerve Suppl; 1995 Apr 01; 3():S102-6. PubMed ID: 7603509
    [Abstract] [Full Text] [Related]

  • 9. Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism.
    Masucci JP, Schon EA, King MP.
    Mol Cell Biochem; 1997 Sep 01; 174(1-2):215-9. PubMed ID: 9309690
    [Abstract] [Full Text] [Related]

  • 10. Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts.
    Cotán D, Cordero MD, Garrido-Maraver J, Oropesa-Ávila M, Rodríguez-Hernández A, Gómez Izquierdo L, De la Mata M, De Miguel M, Lorite JB, Infante ER, Jackson S, Navas P, Sánchez-Alcázar JA.
    FASEB J; 2011 Aug 01; 25(8):2669-87. PubMed ID: 21551238
    [Abstract] [Full Text] [Related]

  • 11. Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.
    Kolesnikova OA, Entelis NS, Jacquin-Becker C, Goltzene F, Chrzanowska-Lightowlers ZM, Lightowlers RN, Martin RP, Tarassov I.
    Hum Mol Genet; 2004 Oct 15; 13(20):2519-34. PubMed ID: 15317755
    [Abstract] [Full Text] [Related]

  • 12. Fibrous dysplasia in a child with mitochondrial A8344G mutation.
    Chen ST, Fan PC, Hwu WL, Wu MH.
    J Child Neurol; 2008 Dec 15; 23(12):1447-50. PubMed ID: 18772492
    [Abstract] [Full Text] [Related]

  • 13. Impaired ROS Scavenging System in Human Induced Pluripotent Stem Cells Generated from Patients with MERRF Syndrome.
    Chou SJ, Tseng WL, Chen CT, Lai YF, Chien CS, Chang YL, Lee HC, Wei YH, Chiou SH.
    Sci Rep; 2016 Mar 30; 6():23661. PubMed ID: 27025901
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial DNA mutation and depletion increase the susceptibility of human cells to apoptosis.
    Liu CY, Lee CF, Hong CH, Wei YH.
    Ann N Y Acad Sci; 2004 Apr 30; 1011():133-45. PubMed ID: 15126291
    [Abstract] [Full Text] [Related]

  • 15. [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
    [Abstract] [Full Text] [Related]

  • 16. Disruption of the human COQ5-containing protein complex is associated with diminished coenzyme Q10 levels under two different conditions of mitochondrial energy deficiency.
    Yen HC, Liu YC, Kan CC, Wei HJ, Lee SH, Wei YH, Feng YH, Chen CW, Huang CC.
    Biochim Biophys Acta; 2016 Sep 30; 1860(9):1864-76. PubMed ID: 27155576
    [Abstract] [Full Text] [Related]

  • 17. 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 30; 41(2-3):256-66. PubMed ID: 20411357
    [Abstract] [Full Text] [Related]

  • 18. Generation of an induced pluripotent stem cell (iPSC) line from a 40-year-old patient with the A8344G mutation of mitochondrial DNA and MERRF (myoclonic epilepsy with ragged red fibers) syndrome.
    Wu YT, Hsu YH, Huang CY, Ho MC, Cheng YC, Wen CH, Ko HW, Lu HE, Chen YC, Tsai CL, Hsu YC, Wei YH, Hsieh PCH.
    Stem Cell Res; 2018 Mar 30; 27():10-14. PubMed ID: 29288969
    [Abstract] [Full Text] [Related]

  • 19. Upregulation of heat shock protein 27 confers resistance to actinomycin D-induced apoptosis in cancer cells.
    Ma W, Teng Y, Hua H, Hou J, Luo T, Jiang Y.
    FEBS J; 2013 Sep 30; 280(18):4612-24. PubMed ID: 23848600
    [Abstract] [Full Text] [Related]

  • 20. Decreased expression of Hsp27 and Hsp70 in transformed lymphoblastoid cells from patients with spinocerebellar ataxia type 7.
    Tsai HF, Lin SJ, Li C, Hsieh M.
    Biochem Biophys Res Commun; 2005 Sep 09; 334(4):1279-86. PubMed ID: 16039988
    [Abstract] [Full Text] [Related]


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