211 related articles for article (PubMed ID: 15146244)
1. Preclinical deposition of pathological prion protein PrPSc in muscles of hamsters orally exposed to scrapie.
Thomzig A; Schulz-Schaeffer W; Kratzel C; Mai J; Beekes M
J Clin Invest; 2004 May; 113(10):1465-72. PubMed ID: 15146244
[TBL] [Abstract][Full Text] [Related]
2. Pathological prion protein in muscles of hamsters and mice infected with rodent-adapted BSE or vCJD.
Thomzig A; Cardone F; Krüger D; Pocchiari M; Brown P; Beekes M
J Gen Virol; 2006 Jan; 87(Pt 1):251-254. PubMed ID: 16361438
[TBL] [Abstract][Full Text] [Related]
3. Widespread PrPSc accumulation in muscles of hamsters orally infected with scrapie.
Thomzig A; Kratzel C; Lenz G; Krüger D; Beekes M
EMBO Rep; 2003 May; 4(5):530-3. PubMed ID: 12776740
[TBL] [Abstract][Full Text] [Related]
4. Accumulation of pathological prion protein PrPSc in the skin of animals with experimental and natural scrapie.
Thomzig A; Schulz-Schaeffer W; Wrede A; Wemheuer W; Brenig B; Kratzel C; Lemmer K; Beekes M
PLoS Pathog; 2007 May; 3(5):e66. PubMed ID: 17530923
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Dimethyl sulfoxide delays PrP sc accumulation and disease symptoms in prion-infected hamsters.
Shaked GM; Engelstein R; Avraham I; Kahana E; Gabizon R
Brain Res; 2003 Sep; 983(1-2):137-43. PubMed ID: 12914974
[TBL] [Abstract][Full Text] [Related]
8. Stability properties of PrP(Sc) from cattle with experimental transmissible spongiform encephalopathies: use of a rapid whole homogenate, protease-free assay.
Vrentas CE; Greenlee JJ; Baron T; Caramelli M; Czub S; Nicholson EM
BMC Vet Res; 2013 Aug; 9():167. PubMed ID: 23945217
[TBL] [Abstract][Full Text] [Related]
9. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.
Raymond GJ; Hope J; Kocisko DA; Priola SA; Raymond LD; Bossers A; Ironside J; Will RG; Chen SG; Petersen RB; Gambetti P; Rubenstein R; Smits MA; Lansbury PT; Caughey B
Nature; 1997 Jul; 388(6639):285-8. PubMed ID: 9230438
[TBL] [Abstract][Full Text] [Related]
10. Prion encephalopathies of animals and humans.
Prusiner SB
Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
[TBL] [Abstract][Full Text] [Related]
11. Computerized morphometric analysis of pathological prion protein deposition in scrapie-infected hamster brain.
Maximova OA; Taffs RE; Pomeroy KL; Piccardo P; Asher DM
J Histochem Cytochem; 2006 Jan; 54(1):97-107. PubMed ID: 16148313
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Prions in skeletal muscle.
Bosque PJ; Ryou C; Telling G; Peretz D; Legname G; DeArmond SJ; Prusiner SB
Proc Natl Acad Sci U S A; 2002 Mar; 99(6):3812-7. PubMed ID: 11904434
[TBL] [Abstract][Full Text] [Related]
14. Seeded fibrillation as molecular basis of the species barrier in human prion diseases.
Luers L; Bannach O; Stöhr J; Wördehoff MM; Wolff M; Nagel-Steger L; Riesner D; Willbold D; Birkmann E
PLoS One; 2013; 8(8):e72623. PubMed ID: 23977331
[TBL] [Abstract][Full Text] [Related]
15. Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy.
Bartz JC; Bessen RA; McKenzie D; Marsh RF; Aiken JM
J Virol; 2000 Jun; 74(12):5542-7. PubMed ID: 10823860
[TBL] [Abstract][Full Text] [Related]
16. Genetic and infectious prion diseases.
Prusiner SB
Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
[TBL] [Abstract][Full Text] [Related]
17. Differences in proteinase K resistance and neuronal deposition of abnormal prion proteins characterize bovine spongiform encephalopathy (BSE) and scrapie strains.
Kuczius T; Groschup MH
Mol Med; 1999 Jun; 5(6):406-18. PubMed ID: 10415165
[TBL] [Abstract][Full Text] [Related]
18. Scrapie, CWD, and Transmissible Mink Encephalopathy.
Mathiason CK
Prog Mol Biol Transl Sci; 2017; 150():267-292. PubMed ID: 28838664
[TBL] [Abstract][Full Text] [Related]
19. Urinary excretion and blood level of prions in scrapie-infected hamsters.
Murayama Y; Yoshioka M; Okada H; Takata M; Yokoyama T; Mohri S
J Gen Virol; 2007 Oct; 88(Pt 10):2890-2898. PubMed ID: 17872544
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
