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Items: 1 to 20 of 98

1.

The extent of protease resistance of misfolded prion protein is highly dependent on the salt concentration.

Concha-Marambio L, Diaz-Espinoza R, Soto C.

J Biol Chem. 2014 Jan 31;289(5):3073-9. doi: 10.1074/jbc.M113.513267. Epub 2013 Dec 12.

2.

Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions.

Saverioni D, Notari S, Capellari S, Poggiolini I, Giese A, Kretzschmar HA, Parchi P.

J Biol Chem. 2013 Sep 27;288(39):27972-85. doi: 10.1074/jbc.M113.477547. Epub 2013 Jul 29.

3.

Kosmotropic anions promote conversion of recombinant prion protein into a PrPSc-like misfolded form.

Diaz-Espinoza R, Mukherjee A, Soto C.

PLoS One. 2012;7(2):e31678. doi: 10.1371/journal.pone.0031678. Epub 2012 Feb 9.

4.

Host Determinants of Prion Strain Diversity Independent of Prion Protein Genotype.

Crowell J, Hughson A, Caughey B, Bessen RA.

J Virol. 2015 Oct;89(20):10427-41. doi: 10.1128/JVI.01586-15. Epub 2015 Aug 5.

5.

In vivo generation of neurotoxic prion protein: role for hsp70 in accumulation of misfolded isoforms.

Fernandez-Funez P, Casas-Tinto S, Zhang Y, Gómez-Velazquez M, Morales-Garza MA, Cepeda-Nieto AC, Castilla J, Soto C, Rincon-Limas DE.

PLoS Genet. 2009 Jun;5(6):e1000507. doi: 10.1371/journal.pgen.1000507. Epub 2009 Jun 5.

6.

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.

7.

PrP(Sc) of scrapie 263K propagates efficiently in spleen and muscle tissues with protein misfolding cyclic amplification.

Shi S, Dong CF, Wang GR, Wang X, An R, Chen JM, Shan B, Zhang BY, Xu K, Shi Q, Tian C, Gao C, Han J, Dong XP.

Virus Res. 2009 Apr;141(1):26-33. doi: 10.1016/j.virusres.2008.12.010. Epub 2009 Jan 20.

PMID:
19162101
8.

Infrared microspectroscopy detects protein misfolding cyclic amplification (PMCA)-induced conformational alterations in hamster scrapie progeny seeds.

Daus ML, Wagenführ K, Thomzig A, Boerner S, Hermann P, Hermelink A, Beekes M, Lasch P.

J Biol Chem. 2013 Dec 6;288(49):35068-80. doi: 10.1074/jbc.M113.497131. Epub 2013 Oct 25.

9.

Conformational stability of mammalian prion protein amyloid fibrils is dictated by a packing polymorphism within the core region.

Cobb NJ, Apostol MI, Chen S, Smirnovas V, Surewicz WK.

J Biol Chem. 2014 Jan 31;289(5):2643-50. doi: 10.1074/jbc.M113.520718. Epub 2013 Dec 12.

10.

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.

11.

In vitro amplification of protease-resistant prion protein requires free sulfhydryl groups.

Lucassen R, Nishina K, Supattapone S.

Biochemistry. 2003 Apr 15;42(14):4127-35.

PMID:
12680767
12.

Generation of genuine prion infectivity by serial PMCA.

Weber P, Giese A, Piening N, Mitteregger G, Thomzig A, Beekes M, Kretzschmar HA.

Vet Microbiol. 2007 Aug 31;123(4):346-57. Epub 2007 Apr 7.

PMID:
17493773
13.

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.

14.

A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.

Pirisinu L, Di Bari M, Marcon S, Vaccari G, D'Agostino C, Fazzi P, Esposito E, Galeno R, Langeveld J, Agrimi U, Nonno R.

PLoS One. 2010 Sep 14;5(9):e12723. doi: 10.1371/journal.pone.0012723.

15.

Generation of prions in vitro and the protein-only hypothesis.

Diaz-Espinoza R, Soto C.

Prion. 2010 Apr-Jun;4(2):53-9. Epub 2010 Apr 5.

16.

Reconstitution of prion infectivity from solubilized protease-resistant PrP and nonprotein components of prion rods.

Shaked GM, Meiner Z, Avraham I, Taraboulos A, Gabizon R.

J Biol Chem. 2001 Apr 27;276(17):14324-8. Epub 2001 Jan 4.

17.

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.

18.

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
19.

Strain-dependent profile of misfolded prion protein aggregates.

Morales R, Hu PP, Duran-Aniotz C, Moda F, Diaz-Espinoza R, Chen B, Bravo-Alegria J, Makarava N, Baskakov IV, Soto C.

Sci Rep. 2016 Feb 15;6:20526. doi: 10.1038/srep20526.

20.

Efficient in vitro amplification of a mouse-adapted scrapie prion protein.

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

Neurosci Lett. 2007 Feb 21;413(3):270-3. Epub 2006 Dec 14.

PMID:
17174030

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