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5. Strain-Dependent Prion Infection in Mice Expressing Prion Protein with Deletion of Central Residues 91-106. Uchiyama K; Miyata H; Yamaguchi Y; Imamura M; Okazaki M; Pasiana AD; Chida J; Hara H; Atarashi R; Watanabe H; Kondoh G; Sakaguchi S Int J Mol Sci; 2020 Oct; 21(19):. PubMed ID: 33019549 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. Weissmann C; Fischer M; Raeber A; Büeler H; Sailer A; Shmerling D; Rülicke T; Brandner S; Aguzzi A Rev Sci Tech; 1998 Apr; 17(1):278-90. PubMed ID: 9638817 [TBL] [Abstract][Full Text] [Related]
8. Prion encephalopathies of animals and humans. Prusiner SB Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114 [TBL] [Abstract][Full Text] [Related]
9. Molecular genetics of transmissible spongiform encephalopathies: an introduction. Weissmann C J Toxicol Sci; 2002 May; 27(2):69-77. PubMed ID: 12058449 [TBL] [Abstract][Full Text] [Related]
10. Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies. Prusiner SB; Groth D; Serban A; Koehler R; Foster D; Torchia M; Burton D; Yang SL; DeArmond SJ Proc Natl Acad Sci U S A; 1993 Nov; 90(22):10608-12. PubMed ID: 7902565 [TBL] [Abstract][Full Text] [Related]
11. Sheep scrapie susceptibility-linked polymorphisms do not modulate the initial binding of cellular to disease-associated prion protein prior to conversion. Rigter A; Bossers A J Gen Virol; 2005 Sep; 86(Pt 9):2627-2634. PubMed ID: 16099922 [TBL] [Abstract][Full Text] [Related]
12. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle. Prusiner SB Dev Biol Stand; 1991; 75():55-74. PubMed ID: 1686599 [TBL] [Abstract][Full Text] [Related]
14. Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality. Coleman BM; Harrison CF; Guo B; Masters CL; Barnham KJ; Lawson VA; Hill AF J Virol; 2014 Mar; 88(5):2690-703. PubMed ID: 24352465 [TBL] [Abstract][Full Text] [Related]
15. Molecular biology and genetics of prion diseases. Prusiner SB Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):447-63. PubMed ID: 7913765 [TBL] [Abstract][Full Text] [Related]
16. Overexpression of nonconvertible PrPc delta114-121 in scrapie-infected mouse neuroblastoma cells leads to trans-dominant inhibition of wild-type PrP(Sc) accumulation. Hölscher C; Delius H; Bürkle A J Virol; 1998 Feb; 72(2):1153-9. PubMed ID: 9445012 [TBL] [Abstract][Full Text] [Related]
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19. Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms. Bossers A; Belt PBGM ; Raymond GJ; Caughey B; de Vries R; Smits MA Proc Natl Acad Sci U S A; 1997 May; 94(10):4931-6. PubMed ID: 9144167 [TBL] [Abstract][Full Text] [Related]
20. Prion protein transgenes and the neuropathology in prion diseases. DeArmond SJ; Prusiner SB Brain Pathol; 1995 Jan; 5(1):77-89. PubMed ID: 7767493 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]