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Items: 1 to 20 of 281

1.

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. doi: 10.1128/JVI.01353-12. Epub 2012 Aug 22.

2.

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. doi: 10.1371/journal.pone.0048969. Epub 2012 Nov 5.

3.

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. doi: 10.1128/JVI.00362-15. Epub 2015 Mar 25.

4.

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 3;91(2). pii: e01686-16. doi: 10.1128/JVI.01686-16. Print 2017 Jan 15.

5.

Cells expressing anchorless prion protein are resistant to scrapie infection.

McNally KL, Ward AE, Priola SA.

J Virol. 2009 May;83(9):4469-75. doi: 10.1128/JVI.02412-08. Epub 2009 Feb 18.

6.

Glycosylphosphatidylinositol anchor-dependent stimulation pathway required for generation of baculovirus-derived recombinant scrapie prion protein.

Imamura M, Kato N, Yoshioka M, Okada H, Iwamaru Y, Shimizu Y, Mohri S, Yokoyama T, Murayama Y.

J Virol. 2011 Mar;85(6):2582-8. doi: 10.1128/JVI.02098-10. Epub 2011 Jan 12.

7.

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. doi: 10.1007/s00401-016-1594-5. Epub 2016 Jul 4.

8.

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 21;289(8):4870-81. doi: 10.1074/jbc.M113.531335. Epub 2014 Jan 7.

9.

De Novo Generation of a Unique Cervid Prion Strain Using Protein Misfolding Cyclic Amplification.

Meyerett-Reid C, Wyckoff AC, Spraker T, Pulford B, Bender H, Zabel MD.

mSphere. 2017 Jan 25;2(1). pii: e00372-16. doi: 10.1128/mSphere.00372-16. eCollection 2017 Jan-Feb.

10.

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 5;6(3):e1000800. doi: 10.1371/journal.ppat.1000800.

11.

Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171.

Striebel JF, Race B, Meade-White KD, LaCasse R, Chesebro B.

PLoS Pathog. 2011 Sep;7(9):e1002275. doi: 10.1371/journal.ppat.1002275. Epub 2011 Sep 29.

12.

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 3;308(5727):1435-9.

13.

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 21;2:8. doi: 10.1186/2051-5960-2-8.

14.

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. doi: 10.1371/journal.ppat.1002746. Epub 2012 Jun 7.

15.

Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains.

Duque Velásquez C, Kim C, Herbst A, Daude N, Garza MC, Wille H, Aiken J, McKenzie D.

J Virol. 2015 Dec;89(24):12362-73. doi: 10.1128/JVI.02010-15. Epub 2015 Sep 30.

16.

Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotype.

Arsac JN, Bétemps D, Morignat E, Féraudet C, Bencsik A, Aubert D, Grassi J, Baron T.

PLoS One. 2009 Oct 6;4(10):e7300. doi: 10.1371/journal.pone.0007300.

17.

Conformational properties of prion strains can be transmitted to recombinant prion protein fibrils in real-time quaking-induced conversion.

Sano K, Atarashi R, Ishibashi D, Nakagaki T, Satoh K, Nishida N.

J Virol. 2014 Oct;88(20):11791-801. doi: 10.1128/JVI.00585-14. Epub 2014 Jul 30.

18.

Recombinant prion protein refolded with lipid and RNA has the biochemical hallmarks of a prion but lacks in vivo infectivity.

Timmes AG, Moore RA, Fischer ER, Priola SA.

PLoS One. 2013 Jul 30;8(7):e71081. doi: 10.1371/journal.pone.0071081. Print 2013.

19.

Infectious prions and proteinopathies.

Barron RM.

Prion. 2017 Jan 2;11(1):40-47. doi: 10.1080/19336896.2017.1283464.

PMID:
28281925
20.

Prions of ruminants show distinct splenotropisms in an ovine transgenic mouse model.

Baron T, Bencsik A, Morignat E.

PLoS One. 2010 Apr 26;5(4):e10310. doi: 10.1371/journal.pone.0010310.

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