Lloyd SE - Search Results

1

Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice.

Lloyd SE, Uphill JB, Targonski PV, Fisher EM, Collinge J. Lloyd SE, et al. Neurogenetics. 2002 Oct;4(2):77-81. doi: 10.1007/s10048-002-0133-9. Neurogenetics. 2002. PMID: 12481985

2

Identification and characterization of a novel mouse prion gene allele.

Lloyd SE, Thompson SR, Beck JA, Linehan JM, Wadsworth JD, Brandner S, Collinge J, Fisher EM. Lloyd SE, et al. Mamm Genome. 2004 May;15(5):383-9. doi: 10.1007/s00335-004-3041-5. Mamm Genome. 2004. PMID: 15170227

3

Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice.

Lloyd SE, Linehan JM, Desbruslais M, Joiner S, Buckell J, Brandner S, Wadsworth JDF, Collinge J. Lloyd SE, et al. J Gen Virol. 2004 Aug;85(Pt 8):2471-2478. doi: 10.1099/vir.0.79889-0. J Gen Virol. 2004. PMID: 15269389

4

Investigation of mcp1 as a quantitative trait gene for prion disease incubation time in mouse.

O'Shea M, Maytham EG, Linehan JM, Brandner S, Collinge J, Lloyd SE. O'Shea M, et al. Among authors: lloyd se. Genetics. 2008 Sep;180(1):559-66. doi: 10.1534/genetics.108.090894. Epub 2008 Aug 20. Genetics. 2008. PMID: 18716327 Free PMC article.

5

A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse.

Lloyd SE, Maytham EG, Grizenkova J, Hummerich H, Collinge J. Lloyd SE, et al. Neurogenetics. 2010 May;11(2):185-91. doi: 10.1007/s10048-009-0219-8. Epub 2009 Oct 1. Neurogenetics. 2010. PMID: 19795140 Free PMC article.

6

Identification of multiple quantitative trait loci linked to prion disease incubation period in mice.

Lloyd SE, Onwuazor ON, Beck JA, Mallinson G, Farrall M, Targonski P, Collinge J, Fisher EM. Lloyd SE, et al. Proc Natl Acad Sci U S A. 2001 May 22;98(11):6279-83. doi: 10.1073/pnas.101130398. Epub 2001 May 15. Proc Natl Acad Sci U S A. 2001. PMID: 11353827 Free PMC article.

7

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.

Asante EA, Linehan JM, Desbruslais M, Joiner S, Gowland I, Wood AL, Welch J, Hill AF, Lloyd SE, Wadsworth JD, Collinge J. Asante EA, et al. Among authors: lloyd se. EMBO J. 2002 Dec 2;21(23):6358-66. doi: 10.1093/emboj/cdf653. EMBO J. 2002. PMID: 12456643 Free PMC article.

8

Human prion protein with valine 129 prevents expression of variant CJD phenotype.

Wadsworth JD, Asante EA, Desbruslais M, Linehan JM, Joiner S, Gowland I, Welch J, Stone L, Lloyd SE, Hill AF, Brandner S, Collinge J. Wadsworth JD, et al. Among authors: lloyd se. Science. 2004 Dec 3;306(5702):1793-6. doi: 10.1126/science.1103932. Epub 2004 Nov 11. Science. 2004. PMID: 15539564

9

HECTD2 is associated with susceptibility to mouse and human prion disease.

Lloyd SE, Maytham EG, Pota H, Grizenkova J, Molou E, Uphill J, Hummerich H, Whitfield J, Alpers MP, Mead S, Collinge J. Lloyd SE, et al. PLoS Genet. 2009 Feb;5(2):e1000383. doi: 10.1371/journal.pgen.1000383. Epub 2009 Feb 13. PLoS Genet. 2009. PMID: 19214206 Free PMC article.

10

Shadoo (Sprn) and prion disease incubation time in mice.

Lloyd SE, Grizenkova J, Pota H, Collinge J. Lloyd SE, et al. Mamm Genome. 2009 Jun;20(6):367-74. doi: 10.1007/s00335-009-9194-5. Epub 2009 Jun 10. Mamm Genome. 2009. PMID: 19513788 Free PMC article.

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