328 related articles for article (PubMed ID: 25810548)
1. Increased infectivity of anchorless mouse scrapie prions in transgenic mice overexpressing human prion protein.
Race B; Phillips K; Meade-White K; Striebel J; Chesebro B
J Virol; 2015 Jun; 89(11):6022-32. PubMed ID: 25810548
[TBL] [Abstract][Full Text] [Related]
2. Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring.
Chesebro B; Race B; Meade-White K; Lacasse R; Race R; Klingeborn M; Striebel J; Dorward D; McGovern G; Jeffrey M
PLoS Pathog; 2010 Mar; 6(3):e1000800. PubMed ID: 20221436
[TBL] [Abstract][Full Text] [Related]
3. Cells expressing anchorless prion protein are resistant to scrapie infection.
McNally KL; Ward AE; Priola SA
J Virol; 2009 May; 83(9):4469-75. PubMed ID: 19225008
[TBL] [Abstract][Full Text] [Related]
4. Distinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion protein.
Rangel A; Race B; Phillips K; Striebel J; Kurtz N; Chesebro B
Acta Neuropathol Commun; 2014 Jan; 2():8. PubMed ID: 24447368
[TBL] [Abstract][Full Text] [Related]
5. Isolation of novel synthetic prion strains by amplification in transgenic mice coexpressing wild-type and anchorless prion proteins.
Raymond GJ; Race B; Hollister JR; Offerdahl DK; Moore RA; Kodali R; Raymond LD; Hughson AG; Rosenke R; Long D; Dorward DW; Baron GS
J Virol; 2012 Nov; 86(21):11763-78. PubMed ID: 22915801
[TBL] [Abstract][Full Text] [Related]
6. PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection.
Marshall KE; Hughson A; Vascellari S; Priola SA; Sakudo A; Onodera T; Baron GS
J Virol; 2017 Jan; 91(2):. PubMed ID: 27847358
[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. Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC.
Vascellari S; Orrù CD; Hughson AG; King D; Barron R; Wilham JM; Baron GS; Race B; Pani A; Caughey B
PLoS One; 2012; 7(11):e48969. PubMed ID: 23139828
[TBL] [Abstract][Full Text] [Related]
9. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S
J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683
[TBL] [Abstract][Full Text] [Related]
10. Crucial role for prion protein membrane anchoring in the neuroinvasion and neural spread of prion infection.
Klingeborn M; Race B; Meade-White KD; Rosenke R; Striebel JF; Chesebro B
J Virol; 2011 Feb; 85(4):1484-94. PubMed ID: 21123371
[TBL] [Abstract][Full Text] [Related]
11. Non-amyloid and amyloid prion protein deposits in prion-infected mice differ in blockage of interstitial brain fluid.
Rangel A; Race B; Striebel J; Chesebro B
Neuropathol Appl Neurobiol; 2013 Apr; 39(3):217-30. PubMed ID: 22998478
[TBL] [Abstract][Full Text] [Related]
12. Scrapie-induced defects in learning and memory of transgenic mice expressing anchorless prion protein are associated with alterations in the gamma aminobutyric acid-ergic pathway.
Trifilo MJ; Sanchez-Alavez M; Solforosi L; Bernard-Trifilo J; Kunz S; McGavern D; Oldstone MB
J Virol; 2008 Oct; 82(20):9890-9. PubMed ID: 18667494
[TBL] [Abstract][Full Text] [Related]
13. Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality.
Coleman BM; Harrison CF; Guo B; Masters CL; Barnham KJ; Lawson VA; Hill AF
J Virol; 2014 Mar; 88(5):2690-703. PubMed ID: 24352465
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Extraneural manifestations of prion infection in GPI-anchorless transgenic mice.
Lee AM; Paulsson JF; Cruite J; Andaya AA; Trifilo MJ; Oldstone MB
Virology; 2011 Mar; 411(1):1-8. PubMed ID: 21227476
[TBL] [Abstract][Full Text] [Related]
16. Propagation of RML prions in mice expressing PrP devoid of GPI anchor leads to formation of a novel, stable prion strain.
Mahal SP; Jablonski J; Suponitsky-Kroyter I; Oelschlegel AM; Herva ME; Oldstone M; Weissmann C
PLoS Pathog; 2012; 8(6):e1002746. PubMed ID: 22685404
[TBL] [Abstract][Full Text] [Related]
17. Amino acid conditions near the GPI anchor attachment site of prion protein for the conversion and the GPI anchoring.
Hizume M; Kobayashi A; Mizusawa H; Kitamoto T
Biochem Biophys Res Commun; 2010 Jan; 391(4):1681-6. PubMed ID: 20040362
[TBL] [Abstract][Full Text] [Related]
18. Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro.
Shen P; Dang J; Wang Z; Zhang W; Yuan J; Lang Y; Ding M; Mitchell M; Kong Q; Feng J; Rozemuller AJM; Cui L; Petersen RB; Zou WQ
Mol Neurobiol; 2021 Jan; 58(1):21-33. PubMed ID: 32889654
[TBL] [Abstract][Full Text] [Related]
19. Overexpression of chimaeric murine/ovine PrP (A136H154Q171) in transgenic mice facilitates transmission and differentiation of ruminant prions.
Griffiths PC; Plater JM; Chave A; Jayasena D; Tout AC; Rice PB; Vickery CM; Spiropoulos J; Stack MJ; Windl O
J Gen Virol; 2013 Nov; 94(Pt 11):2577-2586. PubMed ID: 23761404
[TBL] [Abstract][Full Text] [Related]
20. Prion encephalopathies of animals and humans.
Prusiner SB
Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
