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.
63. Natural and experimental prion diseases of humans and animals. Prusiner SB Curr Opin Neurobiol; 1992 Oct; 2(5):638-47. PubMed ID: 1422120 [TBL] [Abstract][Full Text] [Related]
64. Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease. Meier P; Genoud N; Prinz M; Maissen M; Rülicke T; Zurbriggen A; Raeber AJ; Aguzzi A Cell; 2003 Apr; 113(1):49-60. PubMed ID: 12679034 [TBL] [Abstract][Full Text] [Related]
65. Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies. Kitamoto T; Tateishi J; Tashima T; Takeshita I; Barry RA; DeArmond SJ; Prusiner SB Ann Neurol; 1986 Aug; 20(2):204-8. PubMed ID: 3092727 [TBL] [Abstract][Full Text] [Related]
66. 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]
67. Breaking an absolute species barrier: transgenic mice expressing the mink PrP gene are susceptible to transmissible mink encephalopathy. Windl O; Buchholz M; Neubauer A; Schulz-Schaeffer W; Groschup M; Walter S; Arendt S; Neumann M; Voss AK; Kretzschmar HA J Virol; 2005 Dec; 79(23):14971-5. PubMed ID: 16282497 [TBL] [Abstract][Full Text] [Related]
68. High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene. Büeler H; Raeber A; Sailer A; Fischer M; Aguzzi A; Weissmann C Mol Med; 1994 Nov; 1(1):19-30. PubMed ID: 8790598 [TBL] [Abstract][Full Text] [Related]
69. Re-infection of the prion from the scrapie‑infected cell line SMB-S15 in three strains of mice, CD1, C57BL/6 and Balb/c. Xiao K; Zhang BY; Zhang XM; Wang J; Chen C; Chen LN; Lv Y; Shi Q; Dong XP Int J Mol Med; 2016 Mar; 37(3):716-26. PubMed ID: 26820255 [TBL] [Abstract][Full Text] [Related]
70. Evaluation of infective property of recombinant prion protein amyloids in cultured cells overexpressing cellular prion protein. Kim DH; Lee HM; Ryou C J Korean Med Sci; 2014 Dec; 29(12):1604-9. PubMed ID: 25469058 [TBL] [Abstract][Full Text] [Related]
71. 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 Neurodegeneration; 1994 Dec; 3(4):331-40. PubMed ID: 7842304 [TBL] [Abstract][Full Text] [Related]
72. Genetics of prions. Prusiner SB; Scott MR Annu Rev Genet; 1997; 31():139-75. PubMed ID: 9442893 [TBL] [Abstract][Full Text] [Related]
74. Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity. Telling GC; Parchi P; DeArmond SJ; Cortelli P; Montagna P; Gabizon R; Mastrianni J; Lugaresi E; Gambetti P; Prusiner SB Science; 1996 Dec; 274(5295):2079-82. PubMed ID: 8953038 [TBL] [Abstract][Full Text] [Related]
75. Horse prion protein NMR structure and comparisons with related variants of the mouse prion protein. Pérez DR; Damberger FF; Wüthrich K J Mol Biol; 2010 Jul; 400(2):121-8. PubMed ID: 20460128 [TBL] [Abstract][Full Text] [Related]
76. Susceptibility of transgenic mice expressing chimeric sheep, bovine and human PrP genes to sheep scrapie. Gombojav A; Shimauchi I; Horiuchi M; Ishiguro N; Shinagawa M; Kitamoto T; Miyoshi I; Mohri S; Takata M J Vet Med Sci; 2003 Mar; 65(3):341-7. PubMed ID: 12679564 [TBL] [Abstract][Full Text] [Related]
77. 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]