236 related articles for article (PubMed ID: 24027305)
1. Dissociation of prion protein amyloid seeding from transmission of a spongiform encephalopathy.
Piccardo P; King D; Telling G; Manson JC; Barron RM
J Virol; 2013 Nov; 87(22):12349-56. PubMed ID: 24027305
[TBL] [Abstract][Full Text] [Related]
2. PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions.
Barron RM; King D; Jeffrey M; McGovern G; Agarwal S; Gill AC; Piccardo P
Acta Neuropathol; 2016 Oct; 132(4):611-24. PubMed ID: 27376534
[TBL] [Abstract][Full Text] [Related]
3. Infectious prions and proteinopathies.
Barron RM
Prion; 2017 Jan; 11(1):40-47. PubMed ID: 28281925
[TBL] [Abstract][Full Text] [Related]
4. Mechanism of PrP-amyloid formation in mice without transmissible spongiform encephalopathy.
Jeffrey M; McGovern G; Chambers EV; King D; González L; Manson JC; Ghetti B; Piccardo P; Barron RM
Brain Pathol; 2012 Jan; 22(1):58-66. PubMed ID: 21645162
[TBL] [Abstract][Full Text] [Related]
5. Accumulation of prion protein in the brain that is not associated with transmissible disease.
Piccardo P; Manson JC; King D; Ghetti B; Barron RM
Proc Natl Acad Sci U S A; 2007 Mar; 104(11):4712-7. PubMed ID: 17360589
[TBL] [Abstract][Full Text] [Related]
6. A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy.
Manson JC; Jamieson E; Baybutt H; Tuzi NL; Barron R; McConnell I; Somerville R; Ironside J; Will R; Sy MS; Melton DW; Hope J; Bostock C
EMBO J; 1999 Dec; 18(23):6855-64. PubMed ID: 10581259
[TBL] [Abstract][Full Text] [Related]
7. PrP P102L and Nearby Lysine Mutations Promote Spontaneous
Kraus A; Raymond GJ; Race B; Campbell KJ; Hughson AG; Anson KJ; Raymond LD; Caughey B
J Virol; 2017 Nov; 91(21):. PubMed ID: 28835493
[TBL] [Abstract][Full Text] [Related]
8. Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy.
Katorcha E; Makarava N; Lee YJ; Lindberg I; Monteiro MJ; Kovacs GG; Baskakov IV
PLoS Pathog; 2017 Aug; 13(8):e1006563. PubMed ID: 28797122
[TBL] [Abstract][Full Text] [Related]
9. Kinetics of Abnormal Prion Protein in Blood of Transgenic Mice Experimentally Infected by Multiple Routes with the Agent of Variant Creutzfeldt-Jakob Disease.
Yakovleva O; Pilant T; Asher DM; Gregori L
Viruses; 2023 Jun; 15(7):. PubMed ID: 37515154
[TBL] [Abstract][Full Text] [Related]
10. De novo generation of infectious prions in vitro produces a new disease phenotype.
Barria MA; Mukherjee A; Gonzalez-Romero D; Morales R; Soto C
PLoS Pathog; 2009 May; 5(5):e1000421. PubMed ID: 19436715
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties.
Cancellotti E; Mahal SP; Somerville R; Diack A; Brown D; Piccardo P; Weissmann C; Manson JC
EMBO J; 2013 Mar; 32(5):756-69. PubMed ID: 23395905
[TBL] [Abstract][Full Text] [Related]
13. Host and transmissible spongiform encephalopathy agent strain control glycosylation of PrP.
Somerville RA
J Gen Virol; 1999 Jul; 80 ( Pt 7)():1865-1872. PubMed ID: 10423157
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A single amino acid alteration in murine PrP dramatically alters TSE incubation time.
Manson JC; Barron R; Jamieson E; Baybutt H; Tuzi N; McConnell I; Melton D; Hope J; Bostock C
Arch Virol Suppl; 2000; (16):95-102. PubMed ID: 11214938
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Neuropathology of Animal Prion Diseases.
Orge L; Lima C; Machado C; Tavares P; Mendonça P; Carvalho P; Silva J; Pinto ML; Bastos E; Pereira JC; Gonçalves-Anjo N; Gama A; Esteves A; Alves A; Matos AC; Seixas F; Silva F; Pires I; Figueira L; Vieira-Pinto M; Sargo R; Pires MDA
Biomolecules; 2021 Mar; 11(3):. PubMed ID: 33801117
[TBL] [Abstract][Full Text] [Related]
18. Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein.
Race B; Williams K; Hughson AG; Jansen C; Parchi P; Rozemuller AJM; Chesebro B
Acta Neuropathol Commun; 2018 Feb; 6(1):13. PubMed ID: 29458424
[TBL] [Abstract][Full Text] [Related]
19. Sc237 hamster PrPSc and Sc237-derived mouse PrPSc generated by interspecies in vitro amplification exhibit distinct pathological and biochemical properties in tga20 transgenic mice.
Yoshioka M; Imamura M; Okada H; Shimozaki N; Murayama Y; Yokoyama T; Mohri S
Microbiol Immunol; 2011 May; 55(5):331-40. PubMed ID: 21362027
[TBL] [Abstract][Full Text] [Related]
20. In situ formation of protease-resistant prion protein in transmissible spongiform encephalopathy-infected brain slices.
Bessen RA; Raymond GJ; Caughey B
J Biol Chem; 1997 Jun; 272(24):15227-31. PubMed ID: 9182546
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
