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PUBMED FOR HANDHELDS

Journal Abstract Search

329 related items for PubMed ID: 22949510

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  • 3. Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms.
    Perier C, Bender A, García-Arumí E, Melià MJ, Bové J, Laub C, Klopstock T, Elstner M, Mounsey RB, Teismann P, Prolla T, Andreu AL, Vila M.
    Brain; 2013 Aug; 136(Pt 8):2369-78. PubMed ID: 23884809
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  • 4. Bacterial artificial chromosome transgenic mice expressing a truncated mutant parkin exhibit age-dependent hypokinetic motor deficits, dopaminergic neuron degeneration, and accumulation of proteinase K-resistant alpha-synuclein.
    Lu XH, Fleming SM, Meurers B, Ackerson LC, Mortazavi F, Lo V, Hernandez D, Sulzer D, Jackson GR, Maidment NT, Chesselet MF, Yang XW.
    J Neurosci; 2009 Feb 18; 29(7):1962-76. PubMed ID: 19228951
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  • 6. Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling.
    Goffart S, Cooper HM, Tyynismaa H, Wanrooij S, Suomalainen A, Spelbrink JN.
    Hum Mol Genet; 2009 Jan 15; 18(2):328-40. PubMed ID: 18971204
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  • 8. 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
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  • 9. Preserved striatal innervation maintains motor function despite severe loss of nigral dopaminergic neurons.
    Paß T, Ricke KM, Hofmann P, Chowdhury RS, Nie Y, Chinnery P, Endepols H, Neumaier B, Carvalho A, Rigoux L, Steculorum SM, Prudent J, Riemer T, Aswendt M, Liss B, Brachvogel B, Wiesner RJ.
    Brain; 2024 Sep 03; 147(9):3189-3203. PubMed ID: 38574200
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  • 11. Parkin deficiency exacerbate ethanol-induced dopaminergic neurodegeneration by P38 pathway dependent inhibition of autophagy and mitochondrial function.
    Hwang CJ, Kim YE, Son DJ, Park MH, Choi DY, Park PH, Hellström M, Han SB, Oh KW, Park EK, Hong JT.
    Redox Biol; 2017 Apr 03; 11():456-468. PubMed ID: 28086194
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  • 14. Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice.
    Tyynismaa H, Mjosund KP, Wanrooij S, Lappalainen I, Ylikallio E, Jalanko A, Spelbrink JN, Paetau A, Suomalainen A.
    Proc Natl Acad Sci U S A; 2005 Dec 06; 102(49):17687-92. PubMed ID: 16301523
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  • 16. Repulsive Guidance Molecule a (RGMa) Induces Neuropathological and Behavioral Changes That Closely Resemble Parkinson's Disease.
    Korecka JA, Moloney EB, Eggers R, Hobo B, Scheffer S, Ras-Verloop N, Pasterkamp RJ, Swaab DF, Smit AB, van Kesteren RE, Bossers K, Verhaagen J.
    J Neurosci; 2017 Sep 27; 37(39):9361-9379. PubMed ID: 28842419
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  • 17. PARK14 (D331Y) PLA2G6 Causes Early-Onset Degeneration of Substantia Nigra Dopaminergic Neurons by Inducing Mitochondrial Dysfunction, ER Stress, Mitophagy Impairment and Transcriptional Dysregulation in a Knockin Mouse Model.
    Chiu CC, Lu CS, Weng YH, Chen YL, Huang YZ, Chen RS, Cheng YC, Huang YC, Liu YC, Lai SC, Lin KJ, Lin YW, Chen YJ, Chen CL, Yeh TH, Wang HL.
    Mol Neurobiol; 2019 Jun 27; 56(6):3835-3853. PubMed ID: 30088174
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