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Journal Abstract Search


215 related items for PubMed ID: 18691453

  • 1. Increased expression of Bim contributes to the potentiation of serum deprivation-induced apoptotic cell death in Huntington's disease knock-in striatal cell line.
    Kong PJ, Kil MO, Lee H, Kim SS, Johnson GV, Chun W.
    Neurol Res; 2009 Feb; 31(1):77-83. PubMed ID: 18691453
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  • 2. Calcineurin is involved in the early activation of NMDA-mediated cell death in mutant huntingtin knock-in striatal cells.
    Xifró X, García-Martínez JM, Del Toro D, Alberch J, Pérez-Navarro E.
    J Neurochem; 2008 Jun; 105(5):1596-612. PubMed ID: 18221365
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  • 3. The common inhaled anesthetic isoflurane increases aggregation of huntingtin and alters calcium homeostasis in a cell model of Huntington's disease.
    Wang Q, Liang G, Yang H, Wang S, Eckenhoff MF, Wei H.
    Toxicol Appl Pharmacol; 2011 Feb 01; 250(3):291-8. PubMed ID: 21059370
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  • 4. Differential proteomic and genomic profiling of mouse striatal cell model of Huntington's disease and control; probable implications to the disease biology.
    Choudhury KR, Das S, Bhattacharyya NP.
    J Proteomics; 2016 Jan 30; 132():155-66. PubMed ID: 26581643
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  • 5. Dysregulation of system xc(-) expression induced by mutant huntingtin in a striatal neuronal cell line and in R6/2 mice.
    Frederick NM, Bertho J, Patel KK, Petr GT, Bakradze E, Smith SB, Rosenberg PA.
    Neurochem Int; 2014 Oct 30; 76():59-69. PubMed ID: 25004085
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  • 6. Impaired mitochondrial dynamics and Nrf2 signaling contribute to compromised responses to oxidative stress in striatal cells expressing full-length mutant huntingtin.
    Jin YN, Yu YV, Gundemir S, Jo C, Cui M, Tieu K, Johnson GV.
    PLoS One; 2013 Oct 30; 8(3):e57932. PubMed ID: 23469253
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  • 7. Glutamate transporter expression and function in a striatal neuronal model of Huntington's disease.
    Petr GT, Bakradze E, Frederick NM, Wang J, Armsen W, Aizenman E, Rosenberg PA.
    Neurochem Int; 2013 Jun 30; 62(7):973-81. PubMed ID: 23507328
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  • 8. PH domain leucine-rich repeat protein phosphatase 1 contributes to maintain the activation of the PI3K/Akt pro-survival pathway in Huntington's disease striatum.
    Saavedra A, García-Martínez JM, Xifró X, Giralt A, Torres-Peraza JF, Canals JM, Díaz-Hernández M, Lucas JJ, Alberch J, Pérez-Navarro E.
    Cell Death Differ; 2010 Feb 30; 17(2):324-35. PubMed ID: 19745829
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  • 14. Increased 90-kDa ribosomal S6 kinase (Rsk) activity is protective against mutant huntingtin toxicity.
    Xifró X, Anglada-Huguet M, Rué L, Saavedra A, Pérez-Navarro E, Alberch J.
    Mol Neurodegener; 2011 Oct 31; 6():74. PubMed ID: 22041125
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  • 15. Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis.
    Reis SA, Thompson MN, Lee JM, Fossale E, Kim HH, Liao JK, Moskowitz MA, Shaw SY, Dong L, Haggarty SJ, MacDonald ME, Seong IS.
    Hum Mol Genet; 2011 Jun 15; 20(12):2344-55. PubMed ID: 21447599
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  • 16. Insulin-like growth factor-I blocks Bcl-2 interacting mediator of cell death (Bim) induction and intrinsic death signaling in cerebellar granule neurons.
    Linseman DA, Phelps RA, Bouchard RJ, Le SS, Laessig TA, McClure ML, Heidenreich KA.
    J Neurosci; 2002 Nov 01; 22(21):9287-97. PubMed ID: 12417654
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  • 18. Striatal cells from mutant huntingtin knock-in mice are selectively vulnerable to mitochondrial complex II inhibitor-induced cell death through a non-apoptotic pathway.
    Ruan Q, Lesort M, MacDonald ME, Johnson GV.
    Hum Mol Genet; 2004 Apr 01; 13(7):669-81. PubMed ID: 14962977
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