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Effect of glycans and the glycophosphatidylinositol anchor on strain dependent conformations of scrapie prion protein: improved purifications and infrared spectra.

Baron GS, Hughson AG, Raymond GJ, Offerdahl DK, Barton KA, Raymond LD, Dorward DW, Caughey B.

Biochemistry. 2011 May 31;50(21):4479-90. doi: 10.1021/bi2003907. Epub 2011 May 3.


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.


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.


PrPSc-Specific Antibody Reveals C-Terminal Conformational Differences between Prion Strains.

Saijo E, Hughson AG, Raymond GJ, Suzuki A, Horiuchi M, Caughey B.

J Virol. 2016 Apr 29;90(10):4905-4913. doi: 10.1128/JVI.00088-16. Print 2016 May 15.


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.


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.


Strain-dependent differences in beta-sheet conformations of abnormal prion protein.

Caughey B, Raymond GJ, Bessen RA.

J Biol Chem. 1998 Nov 27;273(48):32230-5.


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.


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 1;411(1):1-8. doi: 10.1016/j.virol.2010.12.012. Epub 2011 Jan 11.


Synergistic and strain-specific effects of bovine spongiform encephalopathy and scrapie prions in the cell-free conversion of recombinant prion protein.

Eiden M, Palm GJ, Hinrichs W, Matthey U, Zahn R, Groschup MH.

J Gen Virol. 2006 Dec;87(Pt 12):3753-61.


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.


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.


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.


A C-terminal protease-resistant prion fragment distinguishes ovine "CH1641-like" scrapie from bovine classical and L-Type BSE in ovine transgenic mice.

Baron T, Bencsik A, Vulin J, Biacabe AG, Morignat E, Verchere J, Betemps D.

PLoS Pathog. 2008 Aug 29;4(8):e1000137. doi: 10.1371/journal.ppat.1000137.


Removal of the glycosylphosphatidylinositol anchor from PrP(Sc) by cathepsin D does not reduce prion infectivity.

Lewis PA, Properzi F, Prodromidou K, Clarke AR, Collinge J, Jackson GS.

Biochem J. 2006 Apr 15;395(2):443-8.


Post-translational modifications in PrP expand the conformational diversity of prions in vivo.

Aguilar-Calvo P, Xiao X, Bett C, Eraña H, Soldau K, Castilla J, Nilsson KP, Surewicz WK, Sigurdson CJ.

Sci Rep. 2017 Mar 8;7:43295. doi: 10.1038/srep43295.


Ultrastructures and strain comparison of under-glycosylated scrapie prion fibrils.

Sim VL, Caughey B.

Neurobiol Aging. 2009 Dec;30(12):2031-42. doi: 10.1016/j.neurobiolaging.2008.02.016. Epub 2008 Apr 3.


Ultrastructure and pathology of prion protein amyloid accumulation and cellular damage in extraneural tissues of scrapie-infected transgenic mice expressing anchorless prion protein.

Race B, Jeffrey M, McGovern G, Dorward D, Chesebro B.

Prion. 2017 Jul 4;11(4):234-248. doi: 10.1080/19336896.2017.1336274. Epub 2017 Jul 31.


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.


Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy.

Caughey BW, Dong A, Bhat KS, Ernst D, Hayes SF, Caughey WS.

Biochemistry. 1991 Aug 6;30(31):7672-80. Erratum in: Biochemistry 1991 Oct 29;30(43):10600.


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