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6. 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; 354(1386):1035-45. PubMed ID: 10434303 [TBL] [Abstract][Full Text] [Related]
7. Caspase cleavage of mutant huntingtin precedes neurodegeneration in Huntington's disease. Wellington CL; Ellerby LM; Gutekunst CA; Rogers D; Warby S; Graham RK; Loubser O; van Raamsdonk J; Singaraja R; Yang YZ; Gafni J; Bredesen D; Hersch SM; Leavitt BR; Roy S; Nicholson DW; Hayden MR J Neurosci; 2002 Sep; 22(18):7862-72. PubMed ID: 12223539 [TBL] [Abstract][Full Text] [Related]
8. Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length. Hansson O; Castilho RF; Korhonen L; Lindholm D; Bates GP; Brundin P J Neurochem; 2001 Aug; 78(4):694-703. PubMed ID: 11520890 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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; 453(7197):921-4. PubMed ID: 18488016 [TBL] [Abstract][Full Text] [Related]
11. 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; 11(4):424-38. PubMed ID: 14713958 [TBL] [Abstract][Full Text] [Related]
12. 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; 285(14):10653-61. PubMed ID: 20145253 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Protection by dietary restriction in the YAC128 mouse model of Huntington's disease: Relation to genes regulating histone acetylation and HTT. Moreno CL; Ehrlich ME; Mobbs CV Neurobiol Dis; 2016 Jan; 85():25-34. PubMed ID: 26485309 [TBL] [Abstract][Full Text] [Related]
16. The Effects of Pharmacological Inhibition of Histone Deacetylase 3 (HDAC3) in Huntington's Disease Mice. Jia H; Wang Y; Morris CD; Jacques V; Gottesfeld JM; Rusche JR; Thomas EA PLoS One; 2016; 11(3):e0152498. PubMed ID: 27031333 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Impaired ubiquitin-proteasome system activity in the synapses of Huntington's disease mice. Wang J; Wang CE; Orr A; Tydlacka S; Li SH; Li XJ J Cell Biol; 2008 Mar; 180(6):1177-89. PubMed ID: 18362179 [TBL] [Abstract][Full Text] [Related]
19. Histone deacetylase inhibitors: a novel therapeutic approach to Huntington's disease (complex mechanism of neuronal death). Sadri-Vakili G; Cha JH Curr Alzheimer Res; 2006 Sep; 3(4):403-8. PubMed ID: 17017871 [TBL] [Abstract][Full Text] [Related]
20. Partial depletion of CREB-binding protein reduces life expectancy in a mouse model of Huntington disease. Klevytska AM; Tebbenkamp AT; Savonenko AV; Borchelt DR J Neuropathol Exp Neurol; 2010 Apr; 69(4):396-404. PubMed ID: 20448484 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]