Collinge J - Search Results

1

A systematic review of prion therapeutics in experimental models.

Trevitt CR, Collinge J. Trevitt CR, et al. Among authors: collinge j. Brain. 2006 Sep;129(Pt 9):2241-65. doi: 10.1093/brain/awl150. Epub 2006 Jul 1. Brain. 2006. PMID: 16816391 Review.

2

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

Poulter M, Baker HF, Frith CD, Leach M, Lofthouse R, Ridley RM, Shah T, Owen F, Collinge J, Brown J, et al. Poulter M, et al. Among authors: collinge j. Brain. 1992 Jun;115 ( Pt 3):675-85. doi: 10.1093/brain/115.3.675. Brain. 1992. PMID: 1352724

3

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

Collinge J, Brown J, Hardy J, Mullan M, Rossor MN, Baker H, Crow TJ, Lofthouse R, Poulter M, Ridley R, et al. Collinge J, et al. Brain. 1992 Jun;115 ( Pt 3):687-710. doi: 10.1093/brain/115.3.687. Brain. 1992. PMID: 1352725

4

Human prion diseases.

Palmer MS, Collinge J. Palmer MS, et al. Among authors: collinge j. Curr Opin Neurol Neurosurg. 1992 Dec;5(6):895-901. Curr Opin Neurol Neurosurg. 1992. PMID: 1467584 Review.

5

Inherited prion diseases.

Collinge J. Collinge J. Adv Neurol. 1993;61:155-65. Adv Neurol. 1993. PMID: 8421966 Review. No abstract available.

6

A prion disease with a novel 96-base pair insertional mutation in the prion protein gene.

Campbell TA, Palmer MS, Will RG, Gibb WR, Luthert PJ, Collinge J. Campbell TA, et al. Among authors: collinge j. Neurology. 1996 Mar;46(3):761-6. doi: 10.1212/wnl.46.3.761. Neurology. 1996. PMID: 8618679

7

Human prion diseases and bovine spongiform encephalopathy (BSE).

Collinge J. Collinge J. Hum Mol Genet. 1997;6(10):1699-705. doi: 10.1093/hmg/6.10.1699. Hum Mol Genet. 1997. PMID: 9300662 Review.

8

Molecular biology of prion propagation.

Wadsworth JD, Jackson GS, Hill AF, Collinge J. Wadsworth JD, et al. Among authors: collinge j. Curr Opin Genet Dev. 1999 Jun;9(3):338-45. doi: 10.1016/s0959-437x(99)80051-3. Curr Opin Genet Dev. 1999. PMID: 10377292 Review.

9

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: collinge j. Brain. 1999 Oct;122 ( Pt 10):1823-37. doi: 10.1093/brain/122.10.1823. Brain. 1999. PMID: 10506086

10

Strain-specific prion-protein conformation determined by metal ions.

Wadsworth JD, Hill AF, Joiner S, Jackson GS, Clarke AR, Collinge J. Wadsworth JD, et al. Among authors: collinge j. Nat Cell Biol. 1999 May;1(1):55-9. doi: 10.1038/9030. Nat Cell Biol. 1999. PMID: 10559865

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