750 related articles for article (PubMed ID: 7913760)
1. The neuropathological phenotype in transgenic mice expressing different prion protein constructs.
DeArmond SJ; Yang SL; Cayetano-Canlas J; Groth D; Prusiner SB
Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):415-23. PubMed ID: 7913760
[TBL] [Abstract][Full Text] [Related]
2. Prion encephalopathies of animals and humans.
Prusiner SB
Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetics of prion diseases and prion diversity in mice.
Carlson GA; DeArmond SJ; Torchia M; Westaway D; Prusiner SB
Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):363-9. PubMed ID: 7913753
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Anchorless prion protein results in infectious amyloid disease without clinical scrapie.
Chesebro B; Trifilo M; Race R; Meade-White K; Teng C; LaCasse R; Raymond L; Favara C; Baron G; Priola S; Caughey B; Masliah E; Oldstone M
Science; 2005 Jun; 308(5727):1435-9. PubMed ID: 15933194
[TBL] [Abstract][Full Text] [Related]
8. Mouse-adapted sporadic human Creutzfeldt-Jakob disease prions propagate in cell culture.
Lawson VA; Vella LJ; Stewart JD; Sharples RA; Klemm H; Machalek DM; Masters CL; Cappai R; Collins SJ; Hill AF
Int J Biochem Cell Biol; 2008; 40(12):2793-801. PubMed ID: 18590830
[TBL] [Abstract][Full Text] [Related]
9. Transgenetic investigations of prion diseases of humans and animals.
Prusiner SB
Philos Trans R Soc Lond B Biol Sci; 1993 Feb; 339(1288):239-54. PubMed ID: 8097053
[TBL] [Abstract][Full Text] [Related]
10. Genetic and infectious prion diseases.
Prusiner SB
Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
[TBL] [Abstract][Full Text] [Related]
11. Dominant-negative inhibition of prion replication in transgenic mice.
Perrier V; Kaneko K; Safar J; Vergara J; Tremblay P; DeArmond SJ; Cohen FE; Prusiner SB; Wallace AC
Proc Natl Acad Sci U S A; 2002 Oct; 99(20):13079-84. PubMed ID: 12271119
[TBL] [Abstract][Full Text] [Related]
12. Molecular biology and transgenetics of prion diseases.
Prusiner SB
Crit Rev Biochem Mol Biol; 1991; 26(5-6):397-438. PubMed ID: 1684745
[TBL] [Abstract][Full Text] [Related]
13. [Mechanisms of neuroinvasion by prions: molecular principles and present state of research].
Brandner S; Klein MA; Aguzzi A
Schweiz Med Wochenschr; 2000 Mar; 130(12):435-42. PubMed ID: 10780058
[TBL] [Abstract][Full Text] [Related]
14. Immunoaffinity purification and neutralization of scrapie prions.
Gabizon R; McKinley MP; Groth D; Westaway D; DeArmond SJ; Carlson GA; Prusiner SB
Prog Clin Biol Res; 1989; 317():583-600. PubMed ID: 2574871
[TBL] [Abstract][Full Text] [Related]
15. Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice.
Pfeifer A; Eigenbrod S; Al-Khadra S; Hofmann A; Mitteregger G; Moser M; Bertsch U; Kretzschmar H
J Clin Invest; 2006 Dec; 116(12):3204-10. PubMed ID: 17143329
[TBL] [Abstract][Full Text] [Related]
16. Reduction of protein kinase MARK4 in the brains of experimental scrapie rodents and human prion disease correlates with deposits of PrP(Sc).
Gong HS; Guo Y; Tian C; Xie WL; Shi Q; Zhang J; Xu Y; Wang SB; Zhang BY; Chen C; Liu Y; Dong XP
Int J Mol Med; 2012 Sep; 30(3):569-78. PubMed ID: 22692785
[TBL] [Abstract][Full Text] [Related]
17. Propagation of ovine prions from "poor" transmitter scrapie isolates in ovine PrP transgenic mice.
Thackray AM; Hopkins L; Lockey R; Spiropoulos J; Bujdoso R
Exp Mol Pathol; 2012 Feb; 92(1):167-74. PubMed ID: 22120785
[TBL] [Abstract][Full Text] [Related]
18. Scrapie-specific neuronal lesions are independent of neuronal PrP expression.
Jeffrey M; Goodsir CM; Race RE; Chesebro B
Ann Neurol; 2004 Jun; 55(6):781-92. PubMed ID: 15174012
[TBL] [Abstract][Full Text] [Related]
19. Scrg1 is induced in TSE and brain injuries, and associated with autophagy.
Dron M; Bailly Y; Beringue V; Haeberlé AM; Griffond B; Risold PY; Tovey MG; Laude H; Dandoy-Dron F
Eur J Neurosci; 2005 Jul; 22(1):133-46. PubMed ID: 16029203
[TBL] [Abstract][Full Text] [Related]
20. Marked influence of the route of infection on prion strain apparent phenotype in a scrapie transgenic mouse model.
Langevin C; Andréoletti O; Le Dur A; Laude H; Béringue V
Neurobiol Dis; 2011 Jan; 41(1):219-25. PubMed ID: 20875860
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]