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. Identification of I137M and other mutations that modulate incubation periods for two human prion strains. Giles K; De Nicola GF; Patel S; Glidden DV; Korth C; Oehler A; DeArmond SJ; Prusiner SB J Virol; 2012 Jun; 86(11):6033-41. PubMed ID: 22438549 [TBL] [Abstract][Full Text] [Related]
5. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene. Korth C; Kaneko K; Groth D; Heye N; Telling G; Mastrianni J; Parchi P; Gambetti P; Will R; Ironside J; Heinrich C; Tremblay P; DeArmond SJ; Prusiner SB Proc Natl Acad Sci U S A; 2003 Apr; 100(8):4784-9. PubMed ID: 12684540 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Telling GC; Scott M; Hsiao KK; Foster D; Yang SL; Torchia M; Sidle KC; Collinge J; DeArmond SJ; Prusiner SB Proc Natl Acad Sci U S A; 1994 Oct; 91(21):9936-40. PubMed ID: 7937921 [TBL] [Abstract][Full Text] [Related]
8. A traceback phenomenon can reveal the origin of prion infection. Kobayashi A; Asano M; Mohri S; Kitamoto T Neuropathology; 2009 Oct; 29(5):619-24. PubMed ID: 19659941 [TBL] [Abstract][Full Text] [Related]
9. Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt-Jakob disease prions is strongly seed and substrate dependent. Bélondrade M; Nicot S; Mayran C; Bruyere-Ostells L; Almela F; Di Bari MA; Levavasseur E; Watts JC; Fournier-Wirth C; Lehmann S; Haïk S; Nonno R; Bougard D Sci Rep; 2021 Feb; 11(1):4058. PubMed ID: 33603091 [TBL] [Abstract][Full Text] [Related]
10. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. Parchi P; Cescatti M; Notari S; Schulz-Schaeffer WJ; Capellari S; Giese A; Zou WQ; Kretzschmar H; Ghetti B; Brown P Brain; 2010 Oct; 133(10):3030-42. PubMed ID: 20823086 [TBL] [Abstract][Full Text] [Related]
11. 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]
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 encephalopathies of animals and humans. Prusiner SB Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease. Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604 [TBL] [Abstract][Full Text] [Related]
16. Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions. Taguchi Y; Mohri S; Ironside JW; Muramoto T; Kitamoto T Am J Pathol; 2003 Dec; 163(6):2585-93. PubMed ID: 14633630 [TBL] [Abstract][Full Text] [Related]
17. Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain. Kobayashi A; Asano M; Mohri S; Kitamoto T J Biol Chem; 2007 Oct; 282(41):30022-8. PubMed ID: 17709374 [TBL] [Abstract][Full Text] [Related]
18. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases. Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565 [TBL] [Abstract][Full Text] [Related]
19. PrP mRNA and protein expression in brain and PrP(c) in CSF in Creutzfeldt-Jakob disease MM1 and VV2. Llorens F; Ansoleaga B; Garcia-Esparcia P; Zafar S; Grau-Rivera O; López-González I; Blanco R; Carmona M; Yagüe J; Nos C; Del Río JA; Gelpí E; Zerr I; Ferrer I Prion; 2013; 7(5):383-93. PubMed ID: 24047819 [TBL] [Abstract][Full Text] [Related]
20. Experimental verification of a traceback phenomenon in prion infection. Kobayashi A; Sakuma N; Matsuura Y; Mohri S; Aguzzi A; Kitamoto T J Virol; 2010 Apr; 84(7):3230-8. PubMed ID: 20089646 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]