Snell RG - Search Results

1

An ovine transgenic Huntington's disease model.

Jacobsen JC, Bawden CS, Rudiger SR, McLaughlan CJ, Reid SJ, Waldvogel HJ, MacDonald ME, Gusella JF, Walker SK, Kelly JM, Webb GC, Faull RL, Rees MI, Snell RG. Jacobsen JC, et al. Among authors: snell rg. Hum Mol Genet. 2010 May 15;19(10):1873-82. doi: 10.1093/hmg/ddq063. Epub 2010 Feb 13. Hum Mol Genet. 2010. PMID: 20154343 Free PMC article.

2

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.

3

MboI RFLP at the D4S43 (C4H) locus.

Lazarou LP, Snell RG, MacDonald ME, Gusella JF, Wasmuth JJ, Shaw DJ. Lazarou LP, et al. Among authors: snell rg. Nucleic Acids Res. 1991 Oct 11;19(19):5445. doi: 10.1093/nar/19.19.5445-a. Nucleic Acids Res. 1991. PMID: 1681512 Free PMC article. No abstract available.

4

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.

Snell RG, MacMillan JC, Cheadle JP, Fenton I, Lazarou LP, Davies P, MacDonald ME, Gusella JF, Harper PS, Shaw DJ. Snell RG, et al. Nat Genet. 1993 Aug;4(4):393-7. doi: 10.1038/ng0893-393. Nat Genet. 1993. PMID: 8401588

5

The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library.

Snell RG, Doucette-Stamm LA, Gillespie KM, Taylor SA, Riba L, Bates GP, Altherr MR, MacDonald ME, Gusella JF, Wasmuth JJ, et al. Snell RG, et al. Hum Mol Genet. 1993 Mar;2(3):305-9. doi: 10.1093/hmg/2.3.305. Hum Mol Genet. 1993. PMID: 8499921

6

Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).

Rees MI, Watts P, Fenton I, Clarke A, Snell RG, Owen MJ, Gray J. Rees MI, et al. Among authors: snell rg. Hum Genet. 2000 Feb;106(2):206-9. doi: 10.1007/s004390051029. Hum Genet. 2000. PMID: 10746562

7

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

8

Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia.

Rees MI, Lewis TM, Vafa B, Ferrie C, Corry P, Muntoni F, Jungbluth H, Stephenson JB, Kerr M, Snell RG, Schofield PR, Owen MJ. Rees MI, et al. Among authors: snell rg. Hum Genet. 2001 Sep;109(3):267-70. doi: 10.1007/s004390100569. Hum Genet. 2001. PMID: 11702206

9

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB).

Rees MI, Lewis TM, Kwok JB, Mortier GR, Govaert P, Snell RG, Schofield PR, Owen MJ. Rees MI, et al. Among authors: snell rg. Hum Mol Genet. 2002 Apr 1;11(7):853-60. doi: 10.1093/hmg/11.7.853. Hum Mol Genet. 2002. PMID: 11929858

10

Insoluble TATA-binding protein accumulation in Huntington's disease cortex.

van Roon-Mom WM, Reid SJ, Jones AL, MacDonald ME, Faull RL, Snell RG. van Roon-Mom WM, et al. Among authors: snell rg. Brain Res Mol Brain Res. 2002 Dec 30;109(1-2):1-10. doi: 10.1016/s0169-328x(02)00450-3. Brain Res Mol Brain Res. 2002. PMID: 12531510

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