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Items: 1 to 20 of 116

1.

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 6;32(5):756-69. doi: 10.1038/emboj.2013.6. Epub 2013 Feb 8.

2.

How independent are TSE agents from their hosts?

Somerville RA.

Prion. 2013 Jul-Aug;7(4):272-5. doi: 10.4161/pri.25420. Epub 2013 Jun 18. Review.

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Host PrP glycosylation: a major factor determining the outcome of prion infection.

Tuzi NL, Cancellotti E, Baybutt H, Blackford L, Bradford B, Plinston C, Coghill A, Hart P, Piccardo P, Barron RM, Manson JC.

PLoS Biol. 2008 Apr 15;6(4):e100. doi: 10.1371/journal.pbio.0060100.

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 15;9:167. doi: 10.1186/1746-6148-9-167.

9.

High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo.

Barron RM, Campbell SL, King D, Bellon A, Chapman KE, Williamson RA, Manson JC.

J Biol Chem. 2007 Dec 7;282(49):35878-86. Epub 2007 Oct 8.

10.

The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between species.

Wiseman FK, Cancellotti E, Piccardo P, Iremonger K, Boyle A, Brown D, Ironside JW, Manson JC, Diack AB.

J Virol. 2015 May;89(9):4738-47. doi: 10.1128/JVI.02296-14. Epub 2015 Feb 11.

11.

Molecular basis of scrapie strain glycoform variation.

Vorberg I, Priola SA.

J Biol Chem. 2002 Sep 27;277(39):36775-81. Epub 2002 Jul 23.

12.

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. doi: 10.1111/j.1348-0421.2011.00328.x.

13.

Dramatic reduction of PrP C level and glycosylation in peripheral nerves following PrP knock-out from Schwann cells does not prevent transmissible spongiform encephalopathy neuroinvasion.

Bradford BM, Tuzi NL, Feltri ML, McCorquodale C, Cancellotti E, Manson JC.

J Neurosci. 2009 Dec 9;29(49):15445-54. doi: 10.1523/JNEUROSCI.4195-09.2009.

14.

Sialylation of prion protein controls the rate of prion amplification, the cross-species barrier, the ratio of PrPSc glycoform and prion infectivity.

Katorcha E, Makarava N, Savtchenko R, D'Azzo A, Baskakov IV.

PLoS Pathog. 2014 Sep 11;10(9):e1004366. doi: 10.1371/journal.ppat.1004366. eCollection 2014 Sep.

15.

Insights into prion strains and neurotoxicity.

Aguzzi A, Heikenwalder M, Polymenidou M.

Nat Rev Mol Cell Biol. 2007 Jul;8(7):552-61. Review.

PMID:
17585315
16.

Disease-associated prion protein in neural and lymphoid tissues of mink (Mustela vison) inoculated with transmissible mink encephalopathy.

Schneider DA, Harrington RD, Zhuang D, Yan H, Truscott TC, Dassanayake RP, O'Rourke KI.

J Comp Pathol. 2012 Nov;147(4):508-21. doi: 10.1016/j.jcpa.2012.03.008. Epub 2012 May 16.

17.

Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein.

Nishida N, Harris DA, Vilette D, Laude H, Frobert Y, Grassi J, Casanova D, Milhavet O, Lehmann S.

J Virol. 2000 Jan;74(1):320-5.

19.

Glycosylation deficiency at either one of the two glycan attachment sites of cellular prion protein preserves susceptibility to bovine spongiform encephalopathy and scrapie infections.

Neuendorf E, Weber A, Saalmueller A, Schatzl H, Reifenberg K, Pfaff E, Groschup MH.

J Biol Chem. 2004 Dec 17;279(51):53306-16. Epub 2004 Sep 23.

20.

Molecular analysis of the protease-resistant prion protein in scrapie and bovine spongiform encephalopathy transmitted to ovine transgenic and wild-type mice.

Baron T, Crozet C, Biacabe AG, Philippe S, Verchere J, Bencsik A, Madec JY, Calavas D, Samarut J.

J Virol. 2004 Jun;78(12):6243-51.

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