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Metabolic disruption identified in the Huntington's disease transgenic sheep model.
Handley RR, Reid SJ, Patassini S, Rudiger SR, Obolonkin V, McLaughlan CJ, Jacobsen JC, Gusella JF, MacDonald ME, Waldvogel HJ, Bawden CS, Faull RL, Snell RG. Handley RR, et al. Among authors: snell rg. Sci Rep. 2016 Feb 11;6:20681. doi: 10.1038/srep20681. Sci Rep. 2016. PMID: 26864449 Free PMC article.
A recombination event that redefines the Huntington disease region.
Snell RG, Thompson LM, Tagle DA, Holloway TL, Barnes G, Harley HG, Sandkuijl LA, MacDonald ME, Collins FS, Gusella JF, et al. Snell RG, et al. Am J Hum Genet. 1992 Aug;51(2):357-62. Am J Hum Genet. 1992. PMID: 1386495 Free PMC article.
Amyloid-like inclusions in Huntington's disease.
McGowan DP, van Roon-Mom W, Holloway H, Bates GP, Mangiarini L, Cooper GJ, Faull RL, Snell RG. McGowan DP, et al. Among authors: snell rg. Neuroscience. 2000;100(4):677-80. doi: 10.1016/s0306-4522(00)00391-2. Neuroscience. 2000. PMID: 11036200
Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia.
Rees MI, Harvey K, Ward H, White JH, Evans L, Duguid IC, Hsu CC, Coleman SL, Miller J, Baer K, Waldvogel HJ, Gibbon F, Smart TG, Owen MJ, Harvey RJ, Snell RG. Rees MI, et al. Among authors: snell rg. J Biol Chem. 2003 Jul 4;278(27):24688-96. doi: 10.1074/jbc.M301070200. Epub 2003 Apr 8. J Biol Chem. 2003. PMID: 12684523 Free article.
134 results