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Journal Abstract Search

434 related items for PubMed ID: 14526190

  • 1. Mechanisms of neuronal cell death in Huntington's disease.
    Sawa A, Tomoda T, Bae BI.
    Cytogenet Genome Res; 2003; 100(1-4):287-95. PubMed ID: 14526190
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  • 2. Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease.
    Reddy PH, Charles V, Williams M, Miller G, Whetsell WO, Tagle DA.
    Philos Trans R Soc Lond B Biol Sci; 1999 Jun 29; 354(1386):1035-45. PubMed ID: 10434303
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  • 3. Specific caspase interactions and amplification are involved in selective neuronal vulnerability in Huntington's disease.
    Hermel E, Gafni J, Propp SS, Leavitt BR, Wellington CL, Young JE, Hackam AS, Logvinova AV, Peel AL, Chen SF, Hook V, Singaraja R, Krajewski S, Goldsmith PC, Ellerby HM, Hayden MR, Bredesen DE, Ellerby LM.
    Cell Death Differ; 2004 Apr 29; 11(4):424-38. PubMed ID: 14713958
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  • 4. Towards a transgenic model of Huntington's disease in a non-human primate.
    Yang SH, Cheng PH, Banta H, Piotrowska-Nitsche K, Yang JJ, Cheng EC, Snyder B, Larkin K, Liu J, Orkin J, Fang ZH, Smith Y, Bachevalier J, Zola SM, Li SH, Li XJ, Chan AW.
    Nature; 2008 Jun 12; 453(7197):921-4. PubMed ID: 18488016
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  • 6. Genetics and neuropathology of Huntington's disease.
    Reiner A, Dragatsis I, Dietrich P.
    Int Rev Neurobiol; 2011 Jun 12; 98():325-72. PubMed ID: 21907094
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  • 7. Pathogenic mechanisms in Huntington's disease.
    Jones L, Hughes A.
    Int Rev Neurobiol; 2011 Jun 12; 98():373-418. PubMed ID: 21907095
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  • 9. Mechanisms for neuronal cell death and dysfunction in Huntington's disease: pathological cross-talk between the nucleus and the mitochondria?
    Sawa A.
    J Mol Med (Berl); 2001 Jul 12; 79(7):375-81. PubMed ID: 11466559
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  • 12. Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
    Kenney C, Powell S, Jankovic J.
    Mov Disord; 2007 Jan 12; 22(1):127-30. PubMed ID: 17115386
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  • 13. Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington's disease.
    Wyttenbach A, Swartz J, Kita H, Thykjaer T, Carmichael J, Bradley J, Brown R, Maxwell M, Schapira A, Orntoft TF, Kato K, Rubinsztein DC.
    Hum Mol Genet; 2001 Aug 15; 10(17):1829-45. PubMed ID: 11532992
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  • 14. Effects on murine behavior and lifespan of selectively decreasing expression of mutant huntingtin allele by supt4h knockdown.
    Cheng HM, Chern Y, Chen IH, Liu CR, Li SH, Chun SJ, Rigo F, Bennett CF, Deng N, Feng Y, Lin CS, Yan YT, Cohen SN, Cheng TH.
    PLoS Genet; 2015 Mar 15; 11(3):e1005043. PubMed ID: 25760041
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  • 15. Mutant huntingtin in glial cells exacerbates neurological symptoms of Huntington disease mice.
    Bradford J, Shin JY, Roberts M, Wang CE, Sheng G, Li S, Li XJ.
    J Biol Chem; 2010 Apr 02; 285(14):10653-61. PubMed ID: 20145253
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  • 16. Lentiviral-mediated delivery of mutant huntingtin in the striatum of rats induces a selective neuropathology modulated by polyglutamine repeat size, huntingtin expression levels, and protein length.
    de Almeida LP, Ross CA, Zala D, Aebischer P, Déglon N.
    J Neurosci; 2002 May 01; 22(9):3473-83. PubMed ID: 11978824
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  • 19. Aggregation in Huntington's disease: insights through modelling.
    Cajavec B, Bernard S, Herzel H.
    Genome Inform; 2005 May 01; 16(1):262-71. PubMed ID: 16362929
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  • 20. Inducing huntingtin inclusion formation in primary neuronal cell culture and in vivo by high-capacity adenoviral vectors expressing truncated and full-length huntingtin with polyglutamine expansion.
    Huang B, Schiefer J, Sass C, Kosinski CM, Kochanek S.
    J Gene Med; 2008 Mar 01; 10(3):269-79. PubMed ID: 18067195
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