241 related articles for article (PubMed ID: 7613755)
1. On safari with PrP: prion diseases of animals.
Westaway D; Carlson GA; Prusiner SB
Trends Microbiol; 1995 Apr; 3(4):141-7. PubMed ID: 7613755
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies.
Weissmann C
FEBS Lett; 1996 Jun; 389(1):3-11. PubMed ID: 8682199
[TBL] [Abstract][Full Text] [Related]
4. Prion encephalopathies of animals and humans.
Prusiner SB
Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
[TBL] [Abstract][Full Text] [Related]
5. Aptamers against prion proteins and prions.
Gilch S; Schätzl HM
Cell Mol Life Sci; 2009 Aug; 66(15):2445-55. PubMed ID: 19396399
[TBL] [Abstract][Full Text] [Related]
6. Prions and prion diseases.
Pergami P; Poloni TE; Corato M; Camisa B; Ceroni M
Funct Neurol; 1999; 14(4):241-52. PubMed ID: 10713898
[No Abstract] [Full Text] [Related]
7. Novel mechanisms of degeneration of the central nervous system--prion structure and biology.
Prusiner SB; Stahl N; DeArmond SJ
Ciba Found Symp; 1988; 135():239-60. PubMed ID: 2900720
[TBL] [Abstract][Full Text] [Related]
8. Allelic Interference in Prion Replication Is Modulated by the Convertibility of the Interfering PrP
Espinosa JC; Andreoletti O; Marín-Moreno A; Lugan S; Aguilar-Calvo P; Cassard H; Lorenzo P; Douet JY; Villa-Díaz A; Aron N; Prieto I; Huor A; Torres JM
mBio; 2021 Mar; 12(2):. PubMed ID: 33727358
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Genetic and infectious prion diseases.
Prusiner SB
Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
[TBL] [Abstract][Full Text] [Related]
12. On the biology of prions.
Prusiner SB; Gabizon R; McKinley MP
Acta Neuropathol; 1987; 72(4):299-314. PubMed ID: 3554880
[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. 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]
15. 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]
16. Environmental and host factors that contribute to prion strain evolution.
Bartz JC
Acta Neuropathol; 2021 Jul; 142(1):5-16. PubMed ID: 33899132
[TBL] [Abstract][Full Text] [Related]
17. Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.
Moreno JA; Telling GC
Methods Mol Biol; 2017; 1658():219-252. PubMed ID: 28861793
[TBL] [Abstract][Full Text] [Related]
18. Evolving views in prion glycosylation: functional and pathological implications.
Ermonval M; Mouillet-Richard S; Codogno P; Kellermann O; Botti J
Biochimie; 2003; 85(1-2):33-45. PubMed ID: 12765773
[TBL] [Abstract][Full Text] [Related]
19. Utility of RNAi-mediated prnp gene silencing in neuroblastoma cells permanently infected by prions: potentials and limitations.
Kim Y; Han B; Titlow W; Mays CE; Kwon M; Ryou C
Antiviral Res; 2009 Nov; 84(2):185-93. PubMed ID: 19748523
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]