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Journal Abstract Search

129 related items for PubMed ID: 31836143

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  • 2. 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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  • 3. The MELAS mutation m.3243A>G promotes reactivation of fetal cardiac genes and an epithelial-mesenchymal transition-like program via dysregulation of miRNAs.
    Meseguer S, Panadero J, Navarro-González C, Villarroya M, Boutoual R, Comi GP, Armengod ME.
    Biochim Biophys Acta Mol Basis Dis; 2018 Sep; 1864(9 Pt B):3022-3037. PubMed ID: 29928977
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  • 4. Modeling of mitochondrial bioenergetics and autophagy impairment in MELAS-mutant iPSC-derived retinal pigment epithelial cells.
    Bhattacharya S, Yin J, Huo W, Chaum E.
    Stem Cell Res Ther; 2022 Jun 17; 13(1):260. PubMed ID: 35715869
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  • 5. 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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  • 6. 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. Mutations of the mitochondrial ND1 gene as a cause of MELAS.
    Kirby DM, McFarland R, Ohtake A, Dunning C, Ryan MT, Wilson C, Ketteridge D, Turnbull DM, Thorburn DR, Taylor RW.
    J Med Genet; 2004 Oct 17; 41(10):784-9. PubMed ID: 15466014
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  • 8. Cell cycle of myocytes of cardiac and skeletal muscle in mitochondrial myopathy.
    Takeda A, Chiba S, Takaaki I, Tanamura A, Yamaguchi Y, Takeda N.
    Jpn Circ J; 1998 Sep 17; 62(9):695-9. PubMed ID: 9766710
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  • 9. Mitochondrial dysfunction and cerebral metabolic abnormalities in patients with mitochondrial encephalomyopathy subtypes: Evidence from proton MR spectroscopy and muscle biopsy.
    Niu FN, Meng HL, Chang LL, Wu HY, Li WP, Liu RY, Wang HT, Zhang B, Xu Y.
    CNS Neurosci Ther; 2017 Aug 17; 23(8):686-697. PubMed ID: 28695670
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  • 10. Pathology of mitochondria in MELAS syndrome: an ultrastructural study.
    Felczak P, Lewandowska E, Stępniak I, Ołdak M, Pollak A, Lechowicz U, Pasennik E, Stępień T, Wierzba-Bobrowicz T.
    Pol J Pathol; 2017 Aug 17; 68(2):173-181. PubMed ID: 29025253
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  • 13. Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation.
    Wang W, Zhuang Q, Ji K, Wen B, Lin P, Zhao Y, Li W, Yan C.
    Sci Rep; 2017 Jan 31; 7():41639. PubMed ID: 28139706
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  • 17. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep 31; 4(5):631-44. PubMed ID: 15347257
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  • 19. Vascular involvement in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
    Takahashi N, Shimada T, Murakami Y, Katoh H, Oyake N, Ishibashi Y, Nishino I, Nonaka I, Goto Y.
    Am J Med Sci; 2005 May 31; 329(5):265-6. PubMed ID: 15894869
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