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5. Expanded-polyglutamine huntingtin protein suppresses the secretion and production of a chemokine (CCL5/RANTES) by astrocytes. Chou SY; Weng JY; Lai HL; Liao F; Sun SH; Tu PH; Dickson DW; Chern Y J Neurosci; 2008 Mar; 28(13):3277-90. PubMed ID: 18367595 [TBL] [Abstract][Full Text] [Related]
6. Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice. Li H; Li SH; Yu ZX; Shelbourne P; Li XJ J Neurosci; 2001 Nov; 21(21):8473-81. PubMed ID: 11606636 [TBL] [Abstract][Full Text] [Related]
7. Genetic manipulations of mutant huntingtin in mice: new insights into Huntington's disease pathogenesis. Lee CY; Cantle JP; Yang XW FEBS J; 2013 Sep; 280(18):4382-94. PubMed ID: 23829302 [TBL] [Abstract][Full Text] [Related]
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9. Mutant huntingtin expression in microglia is neither required nor sufficient to cause the Huntington's disease-like phenotype in BACHD mice. Petkau TL; Hill A; Connolly C; Lu G; Wagner P; Kosior N; Blanco J; Leavitt BR Hum Mol Genet; 2019 May; 28(10):1661-1670. PubMed ID: 30624705 [TBL] [Abstract][Full Text] [Related]
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11. Full length mutant huntingtin is required for altered Ca2+ signaling and apoptosis of striatal neurons in the YAC mouse model of Huntington's disease. Zhang H; Li Q; Graham RK; Slow E; Hayden MR; Bezprozvanny I Neurobiol Dis; 2008 Jul; 31(1):80-8. PubMed ID: 18502655 [TBL] [Abstract][Full Text] [Related]
12. Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease. Valencia A; Reeves PB; Sapp E; Li X; Alexander J; Kegel KB; Chase K; Aronin N; DiFiglia M J Neurosci Res; 2010 Jan; 88(1):179-90. PubMed ID: 19642201 [TBL] [Abstract][Full Text] [Related]
13. Microglial physiological properties and interactions with synapses are altered at presymptomatic stages in a mouse model of Huntington's disease pathology. Savage JC; St-Pierre MK; Carrier M; El Hajj H; Novak SW; Sanchez MG; Cicchetti F; Tremblay MÈ J Neuroinflammation; 2020 Apr; 17(1):98. PubMed ID: 32241286 [TBL] [Abstract][Full Text] [Related]
14. 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]
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16. Cortical efferents lacking mutant huntingtin improve striatal neuronal activity and behavior in a conditional mouse model of Huntington's disease. Estrada-Sánchez AM; Burroughs CL; Cavaliere S; Barton SJ; Chen S; Yang XW; Rebec GV J Neurosci; 2015 Mar; 35(10):4440-51. PubMed ID: 25762686 [TBL] [Abstract][Full Text] [Related]
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19. Disruption of the nuclear membrane by perinuclear inclusions of mutant huntingtin causes cell-cycle re-entry and striatal cell death in mouse and cell models of Huntington's disease. Liu KY; Shyu YC; Barbaro BA; Lin YT; Chern Y; Thompson LM; James Shen CK; Marsh JL Hum Mol Genet; 2015 Mar; 24(6):1602-16. PubMed ID: 25398943 [TBL] [Abstract][Full Text] [Related]
20. Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell-type-specific. Jansen AH; van Hal M; Op den Kelder IC; Meier RT; de Ruiter AA; Schut MH; Smith DL; Grit C; Brouwer N; Kamphuis W; Boddeke HW; den Dunnen WF; van Roon WM; Bates GP; Hol EM; Reits EA Glia; 2017 Jan; 65(1):50-61. PubMed ID: 27615381 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]