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Items: 1 to 20 of 64

1.

Resolution-enhanced native acidic gel electrophoresis: a method for resolving, sizing, and quantifying prion protein oligomers.

Ladner CL, Wishart DS.

Anal Biochem. 2012 Jul 1;426(1):54-62. doi: 10.1016/j.ab.2012.04.005. Epub 2012 Apr 7.

PMID:
22490465
2.
3.

Shaking alone induces de novo conversion of recombinant prion proteins to β-sheet rich oligomers and fibrils.

Ladner-Keay CL, Griffith BJ, Wishart DS.

PLoS One. 2014 Jun 3;9(6):e98753. doi: 10.1371/journal.pone.0098753. eCollection 2014.

4.

Autocatalytic conversion of recombinant prion proteins displays a species barrier.

Baskakov IV.

J Biol Chem. 2004 Feb 27;279(9):7671-7. Epub 2003 Dec 10.

5.

Macromolecular crowding converts the human recombinant PrPC to the soluble neurotoxic beta-oligomers.

Huang L, Jin R, Li J, Luo K, Huang T, Wu D, Wang W, Chen R, Xiao G.

FASEB J. 2010 Sep;24(9):3536-43. doi: 10.1096/fj.09-150987. Epub 2010 Apr 16.

PMID:
20400537
6.

Self-assembly of recombinant prion protein of 106 residues.

Baskakov IV, Aagaard C, Mehlhorn I, Wille H, Groth D, Baldwin MA, Prusiner SB, Cohen FE.

Biochemistry. 2000 Mar 14;39(10):2792-804.

PMID:
10704232
7.

Photo-induced cross-linking of unmodified proteins (PICUP) applied to amyloidogenic peptides.

Rahimi F, Maiti P, Bitan G.

J Vis Exp. 2009 Jan 12;(23). pii: 1071. doi: 10.3791/1071.

8.

Protein misfolding cyclic amplification induces the conversion of recombinant prion protein to PrP oligomers causing neuronal apoptosis.

Yuan Z, Yang L, Chen B, Zhu T, Hassan MF, Yin X, Zhou X, Zhao D.

J Neurochem. 2015 Jun;133(5):722-9. doi: 10.1111/jnc.13098. Epub 2015 Apr 13.

9.

On the mechanism of alpha-helix to beta-sheet transition in the recombinant prion protein.

Morillas M, Vanik DL, Surewicz WK.

Biochemistry. 2001 Jun 12;40(23):6982-7.

PMID:
11389614
10.

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

Swietnicki W, Morillas M, Chen SG, Gambetti P, Surewicz WK.

Biochemistry. 2000 Jan 18;39(2):424-31.

PMID:
10631004
11.
12.

PrP N-terminal domain triggers PrP(Sc)-like aggregation of Dpl.

Erlich P, Cesbron JY, Lemaire-Vieille C, Curt A, Andrieu JP, Schoehn G, Jamin M, Gagnon J.

Biochem Biophys Res Commun. 2008 Jan 18;365(3):478-83. Epub 2007 Nov 13.

PMID:
17997980
13.

Development of oligomeric prion-protein aggregates in a mouse model of prion disease.

Sasaki K, Minaki H, Iwaki T.

J Pathol. 2009 Sep;219(1):123-30. doi: 10.1002/path.2576.

PMID:
19479969
14.

Prion protein oligomers in Creutzfeldt-Jakob disease detected by gel-filtration centrifuge columns.

Minaki H, Sasaki K, Honda H, Iwaki T.

Neuropathology. 2009 Oct;29(5):536-42. doi: 10.1111/j.1440-1789.2009.01007.x. Epub 2009 Mar 3.

PMID:
19389076
15.

Molecular properties of complexes formed between the prion protein and synthetic peptides.

Kaneko K, Wille H, Mehlhorn I, Zhang H, Ball H, Cohen FE, Baldwin MA, Prusiner SB.

J Mol Biol. 1997 Jul 25;270(4):574-86.

PMID:
9245588
16.

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.

PMID:
17098995
17.

Role of polysaccharide and lipid in lipopolysaccharide induced prion protein conversion.

Ladner-Keay CL, LeVatte M, Wishart DS.

Prion. 2016 Nov;10(6):466-483.

18.

In vitro conversion and seeded fibrillization of posttranslationally modified prion protein.

Stöhr J, Elfrink K, Weinmann N, Wille H, Willbold D, Birkmann E, Riesner D.

Biol Chem. 2011 May;392(5):415-21. doi: 10.1515/BC.2011.048.

PMID:
21476870
19.

Photo-induced crosslinking of prion protein oligomers and prions.

Piening N, Weber P, Högen T, Beekes M, Kretzschmar H, Giese A.

Amyloid. 2006 Jun;13(2):67-77.

PMID:
16911960
20.

Assembly of natural and recombinant prion protein into fibrils.

Leffers KW, Wille H, Stöhr J, Junger E, Prusiner SB, Riesner D.

Biol Chem. 2005 Jun;386(6):569-80.

PMID:
16006244

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