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Items: 1 to 20 of 160

1.

Identification of I137M and other mutations that modulate incubation periods for two human prion strains.

Giles K, De Nicola GF, Patel S, Glidden DV, Korth C, Oehler A, DeArmond SJ, Prusiner SB.

J Virol. 2012 Jun;86(11):6033-41. doi: 10.1128/JVI.07027-11. Epub 2012 Mar 21.

2.

Human prion strain selection in transgenic mice.

Giles K, Glidden DV, Patel S, Korth C, Groth D, Lemus A, DeArmond SJ, Prusiner SB.

Ann Neurol. 2010 Aug;68(2):151-61. doi: 10.1002/ana.22104.

3.

Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation.

Watts JC, Giles K, Serban A, Patel S, Oehler A, Bhardwaj S, Guan S, Greicius MD, Miller BL, DeArmond SJ, Geschwind MD, Prusiner SB.

Ann Neurol. 2015 Oct;78(4):540-53. doi: 10.1002/ana.24463. Epub 2015 Aug 25.

4.

Experimental verification of a traceback phenomenon in prion infection.

Kobayashi A, Sakuma N, Matsuura Y, Mohri S, Aguzzi A, Kitamoto T.

J Virol. 2010 Apr;84(7):3230-8. doi: 10.1128/JVI.02387-09. Epub 2010 Jan 20.

5.

A traceback phenomenon can reveal the origin of prion infection.

Kobayashi A, Asano M, Mohri S, Kitamoto T.

Neuropathology. 2009 Oct;29(5):619-24. doi: 10.1111/j.1440-1789.2008.00973.x. Epub 2009 Jul 29.

PMID:
19659941
6.

Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene.

Korth C, Kaneko K, Groth D, Heye N, Telling G, Mastrianni J, Parchi P, Gambetti P, Will R, Ironside J, Heinrich C, Tremblay P, DeArmond SJ, Prusiner SB.

Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4784-9. Epub 2003 Apr 8.

7.

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.

Asante EA, Gowland I, Grimshaw A, Linehan JM, Smidak M, Houghton R, Osiguwa O, Tomlinson A, Joiner S, Brandner S, Wadsworth JD, Collinge J.

J Gen Virol. 2009 Mar;90(Pt 3):546-58. doi: 10.1099/vir.0.007930-0.

8.

Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain.

Kobayashi A, Asano M, Mohri S, Kitamoto T.

J Biol Chem. 2007 Oct 12;282(41):30022-8. Epub 2007 Aug 20.

9.

PrP mRNA and protein expression in brain and PrP(c) in CSF in Creutzfeldt-Jakob disease MM1 and VV2.

Llorens F, Ansoleaga B, Garcia-Esparcia P, Zafar S, Grau-Rivera O, López-González I, Blanco R, Carmona M, Yagüe J, Nos C, Del Río JA, Gelpí E, Zerr I, Ferrer I.

Prion. 2013 Sep-Oct;7(5):383-93. doi: 10.4161/pri.26416. Epub 2013 Sep 18.

10.

Co-occurrence of types 1 and 2 PrP(res) in sporadic Creutzfeldt-Jakob disease MM1.

Kobayashi A, Mizukoshi K, Iwasaki Y, Miyata H, Yoshida Y, Kitamoto T.

Am J Pathol. 2011 Mar;178(3):1309-15. doi: 10.1016/j.ajpath.2010.11.069.

11.

Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.

Galeno R, Di Bari MA, Nonno R, Cardone F, Sbriccoli M, Graziano S, Ingrosso L, Fiorini M, Valanzano A, Pasini G, Poleggi A, Vinci R, Ladogana A, Puopolo M, Monaco S, Agrimi U, Zanusso G, Pocchiari M.

J Virol. 2017 May 12;91(11). pii: e02390-16. doi: 10.1128/JVI.02390-16. Print 2017 Jun 1.

PMID:
28298604
12.

Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions.

Chapuis J, Moudjou M, Reine F, Herzog L, Jaumain E, Chapuis C, Quadrio I, Boulliat J, Perret-Liaudet A, Dron M, Laude H, Rezaei H, Béringue V.

Acta Neuropathol Commun. 2016 Feb 5;4:10. doi: 10.1186/s40478-016-0284-9.

13.

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.

14.

Evidence that bank vole PrP is a universal acceptor for prions.

Watts JC, Giles K, Patel S, Oehler A, DeArmond SJ, Prusiner SB.

PLoS Pathog. 2014 Apr 3;10(4):e1003990. doi: 10.1371/journal.ppat.1003990. eCollection 2014 Apr.

16.

Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions.

Taguchi Y, Mohri S, Ironside JW, Muramoto T, Kitamoto T.

Am J Pathol. 2003 Dec;163(6):2585-93.

17.

Prion encephalopathies of animals and humans.

Prusiner SB.

Dev Biol Stand. 1993;80:31-44. Review.

PMID:
8270114
18.

Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type.

Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G.

Acta Neuropathol. 2006 Nov;112(5):561-71. Epub 2006 Jul 18.

PMID:
16847689
19.

Transmission barriers for bovine, ovine, and human prions in transgenic mice.

Scott MR, Peretz D, Nguyen HO, Dearmond SJ, Prusiner SB.

J Virol. 2005 May;79(9):5259-71.

20.

Chimeric elk/mouse prion proteins in transgenic mice.

Tamgüney G, Giles K, Oehler A, Johnson NL, DeArmond SJ, Prusiner SB.

J Gen Virol. 2013 Feb;94(Pt 2):443-52. doi: 10.1099/vir.0.045989-0. Epub 2012 Oct 24.

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