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Items: 1 to 20 of 145

1.

Conserved properties of human and bovine prion strains on transmission to guinea pigs.

Safar JG, Giles K, Lessard P, Letessier F, Patel S, Serban A, Dearmond SJ, Prusiner SB.

Lab Invest. 2011 Sep;91(9):1326-36. doi: 10.1038/labinvest.2011.89. Epub 2011 Jul 4.

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 Jul 20. pii: JVI.01106-16. [Epub ahead of print]

PMID:
27440899
3.

Genetic and infectious prion diseases.

Prusiner SB.

Arch Neurol. 1993 Nov;50(11):1129-53. Review.

PMID:
8105771
4.

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 2;21(23):6358-66.

5.

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.

7.

Human prion strain selection in transgenic mice.

Giles K, Glidden DV, Patel S, Korth C, Groth D, Lemus A, DeArmond SJ, Prusiner SB.

Ann Neurol. 2010 Aug;68(2):151-61. doi: 10.1002/ana.22104.

8.

Strain-specific viral properties of variant Creutzfeldt-Jakob disease (vCJD) are encoded by the agent and not by host prion protein.

Manuelidis L, Liu Y, Mullins B.

J Cell Biochem. 2009 Feb 1;106(2):220-31. doi: 10.1002/jcb.21988.

9.

Mutant PrPSc conformers induced by a synthetic peptide and several prion strains.

Tremblay P, Ball HL, Kaneko K, Groth D, Hegde RS, Cohen FE, DeArmond SJ, Prusiner SB, Safar JG.

J Virol. 2004 Feb;78(4):2088-99.

10.

Transgenic models of prion disease.

Scott MR, Supattapone S, Nguyen HO, DeArmond SJ, Prusiner SB.

Arch Virol Suppl. 2000;(16):113-24. Review.

PMID:
11214913
11.

Prion encephalopathies of animals and humans.

Prusiner SB.

Dev Biol Stand. 1993;80:31-44. Review.

PMID:
8270114
12.

Resistance of bovine spongiform encephalopathy (BSE) prions to inactivation.

Giles K, Glidden DV, Beckwith R, Seoanes R, Peretz D, DeArmond SJ, Prusiner SB.

PLoS Pathog. 2008 Nov;4(11):e1000206. doi: 10.1371/journal.ppat.1000206. Epub 2008 Nov 14.

13.

Molecular biology and genetics of prion diseases.

Prusiner SB.

Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):447-63. Review.

PMID:
7913765
14.

Alteration of the biological and biochemical characteristics of bovine spongiform encephalopathy prions during interspecies transmission in transgenic mice models.

Yokoyama T, Masujin K, Iwamaru Y, Imamura M, Mohri S.

J Gen Virol. 2009 Jan;90(Pt 1):261-8. doi: 10.1099/vir.0.004754-0.

PMID:
19088297
15.

A traceback phenomenon can reveal the origin of prion infection.

Kobayashi A, Asano M, Mohri S, Kitamoto T.

Neuropathology. 2009 Oct;29(5):619-24. doi: 10.1111/j.1440-1789.2008.00973.x. Epub 2009 Jul 29.

PMID:
19659941
16.

Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type mice.

Ritchie DL, Boyle A, McConnell I, Head MW, Ironside JW, Bruce ME.

J Gen Virol. 2009 Dec;90(Pt 12):3075-82. doi: 10.1099/vir.0.013227-0. Epub 2009 Aug 5.

PMID:
19656962
17.

Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice.

Scott MR, Safar J, Telling G, Nguyen O, Groth D, Torchia M, Koehler R, Tremblay P, Walther D, Cohen FE, DeArmond SJ, Prusiner SB.

Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14279-84.

18.

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.

Asante EA, Gowland I, Grimshaw A, Linehan JM, Smidak M, Houghton R, Osiguwa O, Tomlinson A, Joiner S, Brandner S, Wadsworth JD, Collinge J.

J Gen Virol. 2009 Mar;90(Pt 3):546-58. doi: 10.1099/vir.0.007930-0.

19.

Enhanced virulence of sheep-passaged bovine spongiform encephalopathy agent is revealed by decreased polymorphism barriers in prion protein conversion studies.

Priem J, Langeveld JP, van Keulen LJ, van Zijderveld FG, Andreoletti O, Bossers A.

J Virol. 2014 Mar;88(5):2903-12. doi: 10.1128/JVI.02446-13. Epub 2013 Dec 26.

20.

Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein.

Tamg├╝ney G, Miller MW, Giles K, Lemus A, Glidden DV, DeArmond SJ, Prusiner SB.

J Gen Virol. 2009 Apr;90(Pt 4):1035-47. doi: 10.1099/vir.0.007500-0. Epub 2009 Mar 4.

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