Sidle KC - Search Results

1

Molecular screening of sheep for bovine spongiform encephalopathy.

Hill AF, Sidle KC, Joiner S, Keyes P, Martin TC, Dawson M, Collinge J. Hill AF, et al. Among authors: sidle kc. Neurosci Lett. 1998 Oct 23;255(3):159-62. doi: 10.1016/s0304-3940(98)00736-8. Neurosci Lett. 1998. PMID: 9832197

2

Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein.

Whittington MA, Sidle KC, Gowland I, Meads J, Hill AF, Palmer MS, Jefferys JG, Collinge J. Whittington MA, et al. Among authors: sidle kc. Nat Genet. 1995 Feb;9(2):197-201. doi: 10.1038/ng0295-197. Nat Genet. 1995. PMID: 7719349

3

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.

Telling GC, Scott M, Hsiao KK, Foster D, Yang SL, Torchia M, Sidle KC, Collinge J, DeArmond SJ, Prusiner SB. Telling GC, et al. Among authors: sidle kc. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9936-40. doi: 10.1073/pnas.91.21.9936. Proc Natl Acad Sci U S A. 1994. PMID: 7937921 Free PMC article.

4

Prion protein is necessary for normal synaptic function.

Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR, Jefferys JG. Collinge J, et al. Among authors: sidle kc. Nature. 1994 Jul 28;370(6487):295-7. doi: 10.1038/370295a0. Nature. 1994. PMID: 8035877

5

Deletions in the prion protein gene are not associated with CJD.

Palmer MS, Mahal SP, Campbell TA, Hill AF, Sidle KC, Laplanche JL, Collinge J. Palmer MS, et al. Among authors: sidle kc. Hum Mol Genet. 1993 May;2(5):541-4. doi: 10.1093/hmg/2.5.541. Hum Mol Genet. 1993. PMID: 8100163

6

Inherited prion disease (PrP lysine 200) in Britain: two case reports.

Collinge J, Palmer MS, Campbell T, Sidle KC, Carroll D, Harding A. Collinge J, et al. Among authors: sidle kc. BMJ. 1993 Jan 30;306(6873):301-2. doi: 10.1136/bmj.306.6873.301. BMJ. 1993. PMID: 8461647 Free PMC article.

7

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.

Collinge J, Palmer MS, Sidle KC, Hill AF, Gowland I, Meads J, Asante E, Bradley R, Doey LJ, Lantos PL. Collinge J, et al. Among authors: sidle kc. Nature. 1995 Dec 21-28;378(6559):779-83. doi: 10.1038/378779a0. Nature. 1995. PMID: 8524411

8

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, Will R, Springbett A, Campbell TA, Sidle KC, Palmer MS, Collinge J. Windl O, et al. Among authors: sidle kc. Hum Genet. 1996 Sep;98(3):259-64. doi: 10.1007/s004390050204. Hum Genet. 1996. PMID: 8707291

9

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

Collinge J, Sidle KC, Meads J, Ironside J, Hill AF. Collinge J, et al. Among authors: sidle kc. Nature. 1996 Oct 24;383(6602):685-90. doi: 10.1038/383685a0. Nature. 1996. PMID: 8878476

10

The same prion strain causes vCJD and BSE.

Hill AF, Desbruslais M, Joiner S, Sidle KC, Gowland I, Collinge J, Doey LJ, Lantos P. Hill AF, et al. Among authors: sidle kc. Nature. 1997 Oct 2;389(6650):448-50, 526. doi: 10.1038/38925. Nature. 1997. PMID: 9333232 No abstract available.

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