Hope J - Search Results

1

Mice with gene targetted prion protein alterations show that Prnp, Sinc and Prni are congruent.

Moore RC, Hope J, McBride PA, McConnell I, Selfridge J, Melton DW, Manson JC. Moore RC, et al. Among authors: hope j. Nat Genet. 1998 Feb;18(2):118-25. doi: 10.1038/ng0298-118. Nat Genet. 1998. PMID: 9462739

2

Double replacement gene targeting for the production of a series of mouse strains with different prion protein gene alterations.

Moore RC, Redhead NJ, Selfridge J, Hope J, Manson JC, Melton DW. Moore RC, et al. Among authors: hope j. Biotechnology (N Y). 1995 Sep;13(9):999-1004. doi: 10.1038/nbt0995-999. Biotechnology (N Y). 1995. PMID: 9636277

3

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent.

Bruce ME, Will RG, Ironside JW, McConnell I, Drummond D, Suttie A, McCardle L, Chree A, Hope J, Birkett C, Cousens S, Fraser H, Bostock CJ. Bruce ME, et al. Among authors: hope j. Nature. 1997 Oct 2;389(6650):498-501. doi: 10.1038/39057. Nature. 1997. PMID: 9333239

4

A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy.

Manson JC, Jamieson E, Baybutt H, Tuzi NL, Barron R, McConnell I, Somerville R, Ironside J, Will R, Sy MS, Melton DW, Hope J, Bostock C. Manson JC, et al. Among authors: hope j. EMBO J. 1999 Dec 1;18(23):6855-64. doi: 10.1093/emboj/18.23.6855. EMBO J. 1999. PMID: 10581259 Free PMC article.

5

A single amino acid alteration in murine PrP dramatically alters TSE incubation time.

Manson JC, Barron R, Jamieson E, Baybutt H, Tuzi N, McConnell I, Melton D, Hope J, Bostock C. Manson JC, et al. Among authors: hope j. Arch Virol Suppl. 2000;(16):95-102. doi: 10.1007/978-3-7091-6308-5_8. Arch Virol Suppl. 2000. PMID: 11214938 Review.

6

Are Sinc and the PrP gene congruent? Evidence from PrP gene analysis in Sinc congenic mice.

Hunter N, Dann JC, Bennett AD, Somerville RA, McConnell I, Hope J. Hunter N, et al. Among authors: hope j. J Gen Virol. 1992 Oct;73 ( Pt 10):2751-5. doi: 10.1099/0022-1317-73-10-2751. J Gen Virol. 1992. PMID: 1357080

7

The scrapie fibril protein and its cellular isoform.

Hope J, Manson J. Hope J, et al. Curr Top Microbiol Immunol. 1991;172:57-74. doi: 10.1007/978-3-642-76540-7_4. Curr Top Microbiol Immunol. 1991. PMID: 1687385 Review.

8

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: hope j. J Gen Virol. 1987 Oct;68 ( Pt 10):2711-6. doi: 10.1099/0022-1317-68-10-2711. J Gen Virol. 1987. PMID: 2889794

9

PrP gene dosage determines the timing but not the final intensity or distribution of lesions in scrapie pathology.

Manson JC, Clarke AR, McBride PA, McConnell I, Hope J. Manson JC, et al. Among authors: hope j. Neurodegeneration. 1994 Dec;3(4):331-40. Neurodegeneration. 1994. PMID: 7842304

10

129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal.

Manson JC, Clarke AR, Hooper ML, Aitchison L, McConnell I, Hope J. Manson JC, et al. Among authors: hope j. Mol Neurobiol. 1994 Apr-Jun;8(2-3):121-7. doi: 10.1007/BF02780662. Mol Neurobiol. 1994. PMID: 7999308

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

620 results

Search Page

Filters