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Journal Abstract Search

264 related items for PubMed ID: 32061767

  • 21. Ubiquitin-specific protease USP36 knockdown impairs Parkin-dependent mitophagy via downregulation of Beclin-1-associated autophagy-related ATG14L.
    Geisler S, Jäger L, Golombek S, Nakanishi E, Hans F, Casadei N, Terradas AL, Linnemann C, Kahle PJ.
    Exp Cell Res; 2019 Nov 15; 384(2):111641. PubMed ID: 31550441
    [Abstract] [Full Text] [Related]

  • 22. Regionalized pathology correlates with augmentation of mtDNA copy numbers in a patient with myoclonic epilepsy with ragged-red fibers (MERRF-syndrome).
    Brinckmann A, Weiss C, Wilbert F, von Moers A, Zwirner A, Stoltenburg-Didinger G, Wilichowski E, Schuelke M.
    PLoS One; 2010 Oct 20; 5(10):e13513. PubMed ID: 20976001
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  • 23. Mitochondrial biogenesis: pharmacological approaches.
    Valero T.
    Curr Pharm Des; 2014 Oct 20; 20(35):5507-9. PubMed ID: 24606795
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  • 24. Glutamate excitotoxicity in neurons triggers mitochondrial and endoplasmic reticulum accumulation of Parkin, and, in the presence of N-acetyl cysteine, mitophagy.
    Van Laar VS, Roy N, Liu A, Rajprohat S, Arnold B, Dukes AA, Holbein CD, Berman SB.
    Neurobiol Dis; 2015 Feb 20; 74():180-93. PubMed ID: 25478815
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  • 25. 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
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  • 27. 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 01; 1042():55-63. PubMed ID: 15965045
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  • 28. Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers.
    Chomyn A, Lai ST, Shakeley R, Bresolin N, Scarlato G, Attardi G.
    Am J Hum Genet; 1994 Jun 01; 54(6):966-74. PubMed ID: 8198140
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  • 29. 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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  • 31. Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition.
    Gilkerson RW, De Vries RL, Lebot P, Wikstrom JD, Torgyekes E, Shirihai OS, Przedborski S, Schon EA.
    Hum Mol Genet; 2012 Mar 01; 21(5):978-90. PubMed ID: 22080835
    [Abstract] [Full Text] [Related]

  • 32. 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 Mar 01; 3():S102-6. PubMed ID: 7603509
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  • 33. Lack of Parkin Anticipates the Phenotype and Affects Mitochondrial Morphology and mtDNA Levels in a Mouse Model of Parkinson's Disease.
    Pinto M, Nissanka N, Moraes CT.
    J Neurosci; 2018 Jan 24; 38(4):1042-1053. PubMed ID: 29222404
    [Abstract] [Full Text] [Related]

  • 34. 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
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  • 35. Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutation.
    Blakely EL, Alston CL, Lecky B, Chakrabarti B, Falkous G, Turnbull DM, Taylor RW, Gorman GS.
    Neuromuscul Disord; 2014 Jun 30; 24(6):533-6. PubMed ID: 24792523
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  • 39. Nix restores mitophagy and mitochondrial function to protect against PINK1/Parkin-related Parkinson's disease.
    Koentjoro B, Park JS, Sue CM.
    Sci Rep; 2017 Mar 10; 7():44373. PubMed ID: 28281653
    [Abstract] [Full Text] [Related]

  • 40. Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism.
    Masucci JP, Schon EA, King MP.
    Mol Cell Biochem; 1997 Sep 10; 174(1-2):215-9. PubMed ID: 9309690
    [Abstract] [Full Text] [Related]

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