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Journal Abstract Search

148 related items for PubMed ID: 7846043

  • 1. Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy.
    Moudy AM, Handran SD, Goldberg MP, Ruffin N, Karl I, Kranz-Eble P, DeVivo DC, Rothman SM.
    Proc Natl Acad Sci U S A; 1995 Jan 31; 92(3):729-33. PubMed ID: 7846043
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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 31; 25(8):2669-87. PubMed ID: 21551238
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  • 3. 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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  • 5. 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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  • 9. The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model.
    Frey S, Geffroy G, Desquiret-Dumas V, Gueguen N, Bris C, Belal S, Amati-Bonneau P, Chevrollier A, Barth M, Henrion D, Lenaers G, Bonneau D, Reynier P, Procaccio V.
    Biochim Biophys Acta Mol Basis Dis; 2017 Jan 17; 1863(1):284-291. PubMed ID: 27815040
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  • 10. [Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Liu XL, Bao XH, Ma YN, Chang XZ, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2013 Feb 17; 51(2):130-5. PubMed ID: 23527980
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  • 12. Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies.
    Bonod-Bidaud C, Giraud S, Mandon G, Mousson B, Stepien G.
    Exp Cell Res; 1999 Jan 10; 246(1):91-7. PubMed ID: 9882518
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  • 16. Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.
    Robinson BH, Petrova-Benedict R, Buncic JR, Wallace DC.
    Biochem Med Metab Biol; 1992 Oct 10; 48(2):122-6. PubMed ID: 1329873
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  • 20. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts.
    Hirano M, Pavlakis SG.
    J Child Neurol; 1994 Jan 10; 9(1):4-13. PubMed ID: 8151079
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