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Journal Abstract Search

551 related items for PubMed ID: 21551238

  • 1. 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; 25(8):2669-87. PubMed ID: 21551238
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  • 2. Coenzyme Q deficiency triggers mitochondria degradation by mitophagy.
    Rodríguez-Hernández A, Cordero MD, Salviati L, Artuch R, Pineda M, Briones P, Gómez Izquierdo L, Cotán D, Navas P, Sánchez-Alcázar JA.
    Autophagy; 2009 Jan; 5(1):19-32. PubMed ID: 19115482
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  • 4. Oxidative Insults and Mitochondrial DNA Mutation Promote Enhanced Autophagy and Mitophagy Compromising Cell Viability in Pluripotent Cell Model of Mitochondrial Disease.
    Lin DS, Huang YW, Ho CS, Hung PL, Hsu MH, Wang TJ, Wu TY, Lee TH, Huang ZD, Chang PC, Chiang MF.
    Cells; 2019 Jan 17; 8(1):. PubMed ID: 30658448
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  • 7. Screening of effective pharmacological treatments for MELAS syndrome using yeasts, fibroblasts and cybrid models of the disease.
    Garrido-Maraver J, Cordero MD, Moñino ID, Pereira-Arenas S, Lechuga-Vieco AV, Cotán D, De la Mata M, Oropesa-Ávila M, De Miguel M, Bautista Lorite J, Rivas Infante E, Alvarez-Dolado M, Navas P, Jackson S, Francisci S, Sánchez-Alcázar JA.
    Br J Pharmacol; 2012 Nov 17; 167(6):1311-28. PubMed ID: 22747838
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  • 9. 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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  • 12. Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function.
    Hayashi J, Ohta S, Takai D, Miyabayashi S, Sakuta R, Goto Y, Nonaka I.
    Biochem Biophys Res Commun; 1993 Dec 30; 197(3):1049-55. PubMed ID: 8280119
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  • 13. Effect of rapamycin on mitochondria and lysosomes in fibroblasts from patients with mtDNA mutations.
    Cheema NJ, Cameron JM, Hood DA.
    Am J Physiol Cell Physiol; 2021 Jul 01; 321(1):C176-C186. PubMed ID: 34106788
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  • 17. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.
    Chomyn A, Enriquez JA, Micol V, Fernandez-Silva P, Attardi G.
    J Biol Chem; 2000 Jun 23; 275(25):19198-209. PubMed ID: 10858457
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  • 18. Decreased ATP synthesis is phenotypically expressed during increased energy demand in fibroblasts containing mitochondrial tRNA mutations.
    James AM, Sheard PW, Wei YH, Murphy MP.
    Eur J Biochem; 1999 Jan 23; 259(1-2):462-9. PubMed ID: 9914528
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  • 20. The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.
    Sasarman F, Antonicka H, Shoubridge EA.
    Hum Mol Genet; 2008 Dec 01; 17(23):3697-707. PubMed ID: 18753147
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