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7. 2,4 DNP improves motor function, preserves medium spiny neuronal identity, and reduces oxidative stress in a mouse model of Huntington's disease. Wu B; Jiang M; Peng Q; Li G; Hou Z; Milne GL; Mori S; Alonso R; Geisler JG; Duan W Exp Neurol; 2017 Jul; 293():83-90. PubMed ID: 28359739 [TBL] [Abstract][Full Text] [Related]
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9. Tiagabine is neuroprotective in the N171-82Q and R6/2 mouse models of Huntington's disease. Masuda N; Peng Q; Li Q; Jiang M; Liang Y; Wang X; Zhao M; Wang W; Ross CA; Duan W Neurobiol Dis; 2008 Jun; 30(3):293-302. PubMed ID: 18395459 [TBL] [Abstract][Full Text] [Related]
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11. Neuroprotective effects of probenecid in a transgenic animal model of Huntington's disease. Vamos E; Voros K; Zadori D; Vecsei L; Klivenyi P J Neural Transm (Vienna); 2009 Sep; 116(9):1079-86. PubMed ID: 19551467 [TBL] [Abstract][Full Text] [Related]
12. Mutant huntingtin causes context-dependent neurodegeneration in mice with Huntington's disease. Yu ZX; Li SH; Evans J; Pillarisetti A; Li H; Li XJ J Neurosci; 2003 Mar; 23(6):2193-202. PubMed ID: 12657678 [TBL] [Abstract][Full Text] [Related]
13. A2A receptor knockout worsens survival and motor behaviour in a transgenic mouse model of Huntington's disease. Mievis S; Blum D; Ledent C Neurobiol Dis; 2011 Feb; 41(2):570-6. PubMed ID: 21062644 [TBL] [Abstract][Full Text] [Related]
14. Early white matter abnormalities, progressive brain pathology and motor deficits in a novel knock-in mouse model of Huntington's disease. Jin J; Peng Q; Hou Z; Jiang M; Wang X; Langseth AJ; Tao M; Barker PB; Mori S; Bergles DE; Ross CA; Detloff PJ; Zhang J; Duan W Hum Mol Genet; 2015 May; 24(9):2508-27. PubMed ID: 25609071 [TBL] [Abstract][Full Text] [Related]
15. Small molecule modulator of protein disulfide isomerase attenuates mutant huntingtin toxicity and inhibits endoplasmic reticulum stress in a mouse model of Huntington's disease. Zhou X; Li G; Kaplan A; Gaschler MM; Zhang X; Hou Z; Jiang M; Zott R; Cremers S; Stockwell BR; Duan W Hum Mol Genet; 2018 May; 27(9):1545-1555. PubMed ID: 29462355 [TBL] [Abstract][Full Text] [Related]
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18. Lack of interleukin-1 type 1 receptor enhances the accumulation of mutant huntingtin in the striatum and exacerbates the neurological phenotypes of Huntington's disease mice. Wang CE; Li S; Li XJ Mol Brain; 2010 Nov; 3():33. PubMed ID: 21044321 [TBL] [Abstract][Full Text] [Related]
19. The mGluR5 positive allosteric modulator, CDPPB, ameliorates pathology and phenotypic signs of a mouse model of Huntington's disease. Doria JG; de Souza JM; Andrade JN; Rodrigues HA; Guimaraes IM; Carvalho TG; Guatimosim C; Dobransky T; Ribeiro FM Neurobiol Dis; 2015 Jan; 73():163-73. PubMed ID: 25160573 [TBL] [Abstract][Full Text] [Related]
20. Weight loss in Huntington disease increases with higher CAG repeat number. Aziz NA; van der Burg JM; Landwehrmeyer GB; Brundin P; Stijnen T; ; Roos RA Neurology; 2008 Nov; 71(19):1506-13. PubMed ID: 18981372 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]