These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers. Davenport KA; Henderson DM; Mathiason CK; Hoover EA J Virol; 2016 Dec; 90(23):10752-10761. PubMed ID: 27654299 [TBL] [Abstract][Full Text] [Related]
5. Evidence that bank vole PrP is a universal acceptor for prions. Watts JC; Giles K; Patel S; Oehler A; DeArmond SJ; Prusiner SB PLoS Pathog; 2014 Apr; 10(4):e1003990. PubMed ID: 24699458 [TBL] [Abstract][Full Text] [Related]
6. Soluble polymorphic bank vole prion proteins induced by co-expression of quiescin sulfhydryl oxidase in E. coli and their aggregation behaviors. Abskharon R; Dang J; Elfarash A; Wang Z; Shen P; Zou LS; Hassan S; Wang F; Fujioka H; Steyaert J; Mulaj M; Surewicz WK; Castilla J; Wohlkonig A; Zou WQ Microb Cell Fact; 2017 Oct; 16(1):170. PubMed ID: 28978309 [TBL] [Abstract][Full Text] [Related]
7. Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles. Nonno R; Di Bari MA; Cardone F; Vaccari G; Fazzi P; Dell'Omo G; Cartoni C; Ingrosso L; Boyle A; Galeno R; Sbriccoli M; Lipp HP; Bruce M; Pocchiari M; Agrimi U PLoS Pathog; 2006 Feb; 2(2):e12. PubMed ID: 16518470 [TBL] [Abstract][Full Text] [Related]
8. The utility of bank voles for studying prion disease. Arshad H; Bourkas MEC; Watts JC Prog Mol Biol Transl Sci; 2020; 175():179-211. PubMed ID: 32958232 [TBL] [Abstract][Full Text] [Related]
9. Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivo. Piening N; Nonno R; Di Bari M; Walter S; Windl O; Agrimi U; Kretzschmar HA; Bertsch U J Biol Chem; 2006 Apr; 281(14):9373-84. PubMed ID: 16455657 [TBL] [Abstract][Full Text] [Related]
10. Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins. Asante EA; Gowland I; Grimshaw A; Linehan JM; Smidak M; Houghton R; Osiguwa O; Tomlinson A; Joiner S; Brandner S; Wadsworth JDF; Collinge J J Gen Virol; 2009 Mar; 90(Pt 3):546-558. PubMed ID: 19218199 [TBL] [Abstract][Full Text] [Related]
12. Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions. Chapuis J; Moudjou M; Reine F; Herzog L; Jaumain E; Chapuis C; Quadrio I; Boulliat J; Perret-Liaudet A; Dron M; Laude H; Rezaei H; Béringue V Acta Neuropathol Commun; 2016 Feb; 4():10. PubMed ID: 26847207 [TBL] [Abstract][Full Text] [Related]
13. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice. Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443 [TBL] [Abstract][Full Text] [Related]
14. Prion protein amino acid determinants of differential susceptibility and molecular feature of prion strains in mice and voles. PLoS Pathog; ; . PubMed ID: 18654630 [TBL] [Abstract][Full Text] [Related]