295 related articles for article (PubMed ID: 18234793)
1. Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.
Kong Q; Zheng M; Casalone C; Qing L; Huang S; Chakraborty B; Wang P; Chen F; Cali I; Corona C; Martucci F; Iulini B; Acutis P; Wang L; Liang J; Wang M; Li X; Monaco S; Zanusso G; Zou WQ; Caramelli M; Gambetti P
J Virol; 2008 Apr; 82(7):3697-701. PubMed ID: 18234793
[TBL] [Abstract][Full Text] [Related]
2. Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.
Watts JC; Giles K; Saltzberg DJ; Dugger BN; Patel S; Oehler A; Bhardwaj S; Sali A; Prusiner SB
J Virol; 2016 Nov; 90(21):9558-9569. PubMed ID: 27440899
[TBL] [Abstract][Full Text] [Related]
3. Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice.
Jaumain E; Quadrio I; Herzog L; Reine F; Rezaei H; Andréoletti O; Laude H; Perret-Liaudet A; Haïk S; Béringue V
J Virol; 2016 Dec; 90(23):10867-10874. PubMed ID: 27681129
[TBL] [Abstract][Full Text] [Related]
4. Presence of subclinical infection in gene-targeted human prion protein transgenic mice exposed to atypical bovine spongiform encephalopathy.
Wilson R; Dobie K; Hunter N; Casalone C; Baron T; Barron RM
J Gen Virol; 2013 Dec; 94(Pt 12):2819-2827. PubMed ID: 24045112
[TBL] [Abstract][Full Text] [Related]
5. Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.
Scott MR; Will R; Ironside J; Nguyen HO; Tremblay P; DeArmond SJ; Prusiner SB
Proc Natl Acad Sci U S A; 1999 Dec; 96(26):15137-42. PubMed ID: 10611351
[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. Transgenic models of prion disease.
Scott MR; Supattapone S; Nguyen HO; DeArmond SJ; Prusiner SB
Arch Virol Suppl; 2000; (16):113-24. PubMed ID: 11214913
[TBL] [Abstract][Full Text] [Related]
8. Experimental Infection of Cattle With a Novel Prion Derived From Atypical H-Type Bovine Spongiform Encephalopathy.
Okada H; Masujin K; Miyazawa K; Iwamaru Y; Imamura M; Matsuura Y; Arai S; Fukuda S; Murayama Y; Yokoyama T
Vet Pathol; 2017 Nov; 54(6):892-900. PubMed ID: 28731378
[TBL] [Abstract][Full Text] [Related]
9. Transmission barriers for bovine, ovine, and human prions in transgenic mice.
Scott MR; Peretz D; Nguyen HO; Dearmond SJ; Prusiner SB
J Virol; 2005 May; 79(9):5259-71. PubMed ID: 15827140
[TBL] [Abstract][Full Text] [Related]
10. Emergence of a novel bovine spongiform encephalopathy (BSE) prion from an atypical H-type BSE.
Masujin K; Okada H; Miyazawa K; Matsuura Y; Imamura M; Iwamaru Y; Murayama Y; Yokoyama T
Sci Rep; 2016 Mar; 6():22753. PubMed ID: 26948374
[TBL] [Abstract][Full Text] [Related]
11. Tracking and clarifying differential traits of classical- and atypical L-type bovine spongiform encephalopathy prions after transmission from cattle to cynomolgus monkeys.
Hagiwara K; Sato Y; Yamakawa Y; Hara H; Tobiume M; Okemoto-Nakamura Y; Sata T; Horiuchi M; Shibata H; Ono F
PLoS One; 2019; 14(5):e0216807. PubMed ID: 31095605
[TBL] [Abstract][Full Text] [Related]
12. Bovine PrP expression levels in transgenic mice influence transmission characteristics of atypical bovine spongiform encephalopathy.
Wilson R; Hart P; Piccardo P; Hunter N; Casalone C; Baron T; Barron RM
J Gen Virol; 2012 May; 93(Pt 5):1132-1140. PubMed ID: 22302882
[TBL] [Abstract][Full Text] [Related]
13. Unique properties of the classical bovine spongiform encephalopathy strain and its emergence from H-type bovine spongiform encephalopathy substantiated by VM transmission studies.
Bencsik A; Leboidre M; Debeer S; Aufauvre C; Baron T
J Neuropathol Exp Neurol; 2013 Mar; 72(3):211-8. PubMed ID: 23399901
[TBL] [Abstract][Full Text] [Related]
14. Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
Capobianco R; Casalone C; Suardi S; Mangieri M; Miccolo C; Limido L; Catania M; Rossi G; Di Fede G; Giaccone G; Bruzzone MG; Minati L; Corona C; Acutis P; Gelmetti D; Lombardi G; Groschup MH; Buschmann A; Zanusso G; Monaco S; Caramelli M; Tagliavini F
PLoS Pathog; 2007 Mar; 3(3):e31. PubMed ID: 17352534
[TBL] [Abstract][Full Text] [Related]
15. BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.
Asante EA; Linehan JM; Desbruslais M; Joiner S; Gowland I; Wood AL; Welch J; Hill AF; Lloyd SE; Wadsworth JD; Collinge J
EMBO J; 2002 Dec; 21(23):6358-66. PubMed ID: 12456643
[TBL] [Abstract][Full Text] [Related]
16. Radical Change in Zoonotic Abilities of Atypical BSE Prion Strains as Evidenced by Crossing of Sheep Species Barrier in Transgenic Mice.
Marín-Moreno A; Huor A; Espinosa JC; Douet JY; Aguilar-Calvo P; Aron N; Píquer J; Lugan S; Lorenzo P; Tillier C; Cassard H; Andreoletti O; Torres JM
Emerg Infect Dis; 2020 Jun; 26(6):1130-1139. PubMed ID: 32441630
[TBL] [Abstract][Full Text] [Related]
17. Transmissibility of H-Type Bovine Spongiform Encephalopathy to Hamster PrP Transgenic Mice.
Okada H; Masujin K; Miyazawa K; Yokoyama T
PLoS One; 2015; 10(10):e0138977. PubMed ID: 26466381
[TBL] [Abstract][Full Text] [Related]
18. Differentiation of prions from L-type BSE versus sporadic Creutzfeldt-Jakob disease.
Nicot S; Bencsik A; Morignat E; Mestre-Francés N; Perret-Liaudet A; Baron T
Emerg Infect Dis; 2012 Dec; 18(12):2028-31. PubMed ID: 23171544
[TBL] [Abstract][Full Text] [Related]
19. Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.
Collinge J; Palmer MS; Sidle KC; Hill AF; Gowland I; Meads J; Asante E; Bradley R; Doey LJ; Lantos PL
Nature; 1995 Dec 21-28; 378(6559):779-83. PubMed ID: 8524411
[TBL] [Abstract][Full Text] [Related]
20. Bovine spongiform encephalopathy induces misfolding of alleged prion-resistant species cellular prion protein without altering its pathobiological features.
Vidal E; Fernández-Borges N; Pintado B; Ordóñez M; Márquez M; Fondevila D; Torres JM; Pumarola M; Castilla J
J Neurosci; 2013 May; 33(18):7778-86. PubMed ID: 23637170
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]