Dickinson A - Search Results

1

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Mead S, et al. Among authors: dickinson a. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

2

Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia.

Beck JA, Mead S, Campbell TA, Dickinson A, Wientjens DP, Croes EA, Van Duijn CM, Collinge J. Beck JA, et al. Among authors: dickinson a. Neurology. 2001 Jul 24;57(2):354-6. doi: 10.1212/wnl.57.2.354. Neurology. 2001. PMID: 11468331

3

Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations.

Hill AF, Joiner S, Beck JA, Campbell TA, Dickinson A, Poulter M, Wadsworth JD, Collinge J. Hill AF, et al. Among authors: dickinson a. Brain. 2006 Mar;129(Pt 3):676-85. doi: 10.1093/brain/awl013. Epub 2006 Jan 16. Brain. 2006. PMID: 16415305

4

Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.

Mallucci GR, Campbell TA, Dickinson A, Beck J, Holt M, Plant G, de Pauw KW, Hakin RN, Clarke CE, Howell S, Davies-Jones GA, Lawden M, Smith CM, Ince P, Ironside JW, Bridges LR, Dean A, Weeks I, Collinge J. Mallucci GR, et al. Among authors: dickinson a. Brain. 1999 Oct;122 ( Pt 10):1823-37. doi: 10.1093/brain/122.10.1823. Brain. 1999. PMID: 10506086

5

Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

Mallucci G, Dickinson A, Linehan J, Klöhn PC, Brandner S, Collinge J. Mallucci G, et al. Among authors: dickinson a. Science. 2003 Oct 31;302(5646):871-4. doi: 10.1126/science.1090187. Science. 2003. PMID: 14593181

6

Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice.

Mallucci GR, White MD, Farmer M, Dickinson A, Khatun H, Powell AD, Brandner S, Jefferys JG, Collinge J. Mallucci GR, et al. Among authors: dickinson a. Neuron. 2007 Feb 1;53(3):325-35. doi: 10.1016/j.neuron.2007.01.005. Neuron. 2007. PMID: 17270731 Free article.

7

Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.

Janssen JC, Hall M, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell T, Collinge J, Lantos PL, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: dickinson a. Brain. 2000 May;123 ( Pt 5):894-907. doi: 10.1093/brain/123.5.894. Brain. 2000. PMID: 10775535

8

Early onset familial Alzheimer's disease: Mutation frequency in 31 families.

Janssen JC, Beck JA, Campbell TA, Dickinson A, Fox NC, Harvey RJ, Houlden H, Rossor MN, Collinge J. Janssen JC, et al. Among authors: dickinson a. Neurology. 2003 Jan 28;60(2):235-9. doi: 10.1212/01.wnl.0000042088.22694.e3. Neurology. 2003. PMID: 12552037

9

Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation.

Janssen JC, Lantos PL, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell TA, Collinge J, Hanger DP, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: dickinson a. Arch Neurol. 2001 Jun;58(6):953-8. doi: 10.1001/archneur.58.6.953. Arch Neurol. 2001. PMID: 11405810

10

Linkage of the scrapie-associated fibril protein (PrP) gene and Sinc using congenic mice and restriction fragment length polymorphism analysis.

Hunter N, Hope J, McConnell I, Dickinson AG. Hunter N, et al. Among authors: dickinson ag. J Gen Virol. 1987 Oct;68 ( Pt 10):2711-6. doi: 10.1099/0022-1317-68-10-2711. J Gen Virol. 1987. PMID: 2889794

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