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Items: 1 to 20 of 81

1.

Naturally prion resistant mammals: a utopia?

Fernández-Borges N, Chianini F, Eraña H, Vidal E, Eaton SL, Pintado B, Finlayson J, Dagleish MP, Castilla J.

Prion. 2012 Nov-Dec;6(5):425-9. doi: 10.4161/pri.22057.

2.

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.

3.

Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease.

Makarava N, Kovacs GG, Savtchenko R, Alexeeva I, Budka H, Rohwer RG, Baskakov IV.

PLoS Pathog. 2011 Dec;7(12):e1002419. doi: 10.1371/journal.ppat.1002419.

4.

Quaternary structure of pathological prion protein as a determining factor of strain-specific prion replication dynamics.

Laferrière F, Tixador P, Moudjou M, Chapuis J, Sibille P, Herzog L, Reine F, Jaumain E, Laude H, Rezaei H, Béringue V.

PLoS Pathog. 2013;9(10):e1003702. doi: 10.1371/journal.ppat.1003702.

5.

Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease.

Meier P, Genoud N, Prinz M, Maissen M, Rülicke T, Zurbriggen A, Raeber AJ, Aguzzi A.

Cell. 2003 Apr 4;113(1):49-60.

6.

The N-terminal sequence of prion protein consists an epitope specific to the abnormal isoform of prion protein (PrP(Sc)).

Masujin K, Kaku-Ushiki Y, Miwa R, Okada H, Shimizu Y, Kasai K, Matsuura Y, Yokoyama T.

PLoS One. 2013;8(2):e58013. doi: 10.1371/journal.pone.0058013.

7.

Protease-resistant prions selectively decrease Shadoo protein.

Watts JC, Stöhr J, Bhardwaj S, Wille H, Oehler A, Dearmond SJ, Giles K, Prusiner SB.

PLoS Pathog. 2011 Nov;7(11):e1002382. doi: 10.1371/journal.ppat.1002382.

8.

Cell-free propagation of prion strains.

Castilla J, Morales R, Saá P, Barria M, Gambetti P, Soto C.

EMBO J. 2008 Oct 8;27(19):2557-66. doi: 10.1038/emboj.2008.181.

9.

The region approximately between amino acids 81 and 137 of proteinase K-resistant PrPSc is critical for the infectivity of the Chandler prion strain.

Shindoh R, Kim CL, Song CH, Hasebe R, Horiuchi M.

J Virol. 2009 Apr;83(8):3852-60. doi: 10.1128/JVI.01740-08.

10.

The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases.

Schulz-Schaeffer WJ, Tschöke S, Kranefuss N, Dröse W, Hause-Reitner D, Giese A, Groschup MH, Kretzschmar HA.

Am J Pathol. 2000 Jan;156(1):51-6.

11.

[Mechanisms of prion transmission].

Sakaguchi S.

Nihon Rinsho. 2007 Aug;65(8):1391-5. Review. Japanese.

PMID:
17695274
12.

Species-barrier-independent prion replication in apparently resistant species.

Hill AF, Collinge J.

APMIS. 2002 Jan;110(1):44-53. Review.

PMID:
12064255
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
15.

Bovine spongiform encephalopathy induces misfolding of alleged prion-resistant species cellular prion protein without altering its pathobiological features.

Vidal E, Fernández-Borges N, Pintado B, Ordóñez M, Márquez M, Fondevila D, Torres JM, Pumarola M, Castilla J.

J Neurosci. 2013 May 1;33(18):7778-86. doi: 10.1523/JNEUROSCI.0244-13.2013.

16.
17.

Tracing conformational transition of abnormal prion proteins during interspecies transmission by using novel antibodies.

Ushiki-Kaku Y, Endo R, Iwamaru Y, Shimizu Y, Imamura M, Masujin K, Yamamoto T, Hattori S, Itohara S, Irie S, Yokoyama T.

J Biol Chem. 2010 Apr 16;285(16):11931-6. doi: 10.1074/jbc.M109.058859.

18.

Cell-specific susceptibility to prion strains is a property of the intact cell.

Herva ME, Weissman C.

Prion. 2012 Sep-Oct;6(4):371-4. doi: 10.4161/pri.20198.

19.

Increased proportions of C1 truncated prion protein protect against cellular M1000 prion infection.

Lewis V, Hill AF, Haigh CL, Klug GM, Masters CL, Lawson VA, Collins SJ.

J Neuropathol Exp Neurol. 2009 Oct;68(10):1125-35. doi: 10.1097/NEN.0b013e3181b96981.

20.

Prion protein functions and dysfunction in prion diseases.

Sakudo A, Ikuta K.

Curr Med Chem. 2009;16(3):380-9. Review.

PMID:
19149584
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