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Items: 1 to 20 of 70

1.

Lichens: unexpected anti-prion agents?

Rodriguez CM, Bennett JP, Johnson CJ.

Prion. 2012 Jan-Mar;6(1):11-6. doi: 10.4161/pri.6.1.17414. Review.

2.

Degradation of the disease-associated prion protein by a serine protease from lichens.

Johnson CJ, Bennett JP, Biro SM, Duque-Velasquez JC, Rodriguez CM, Bessen RA, Rocke TE.

PLoS One. 2011 May 11;6(5):e19836. doi: 10.1371/journal.pone.0019836.

3.

Detection of protease-resistant cervid prion protein in water from a CWD-endemic area.

Nichols TA, Pulford B, Wyckoff AC, Meyerett C, Michel B, Gertig K, Hoover EA, Jewell JE, Telling GC, Zabel MD.

Prion. 2009 Jul-Sep;3(3):171-83. Epub 2009 Jul 14.

4.

[Biology of non-conventional transmissible agents or prions].

Dormont D.

Rev Neurol (Paris). 1998 Feb;154(2):142-51. Review. French.

PMID:
9773035
5.

Direct detection of soil-bound prions.

Genovesi S, Leita L, Sequi P, Andrighetto I, Sorgato MC, Bertoli A.

PLoS One. 2007 Oct 24;2(10):e1069.

6.

The elk PRNP codon 132 polymorphism controls cervid and scrapie prion propagation.

Green KM, Browning SR, Seward TS, Jewell JE, Ross DL, Green MA, Williams ES, Hoover EA, Telling GC.

J Gen Virol. 2008 Feb;89(Pt 2):598-608. doi: 10.1099/vir.0.83168-0.

PMID:
18198392
7.

Prion encephalopathies of animals and humans.

Prusiner SB.

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

PMID:
8270114
8.

Prion protein adsorption to soil in a competitive matrix is slow and reduced.

Saunders SE, Bartz JC, Bartelt-Hunt SL.

Environ Sci Technol. 2009 Oct 15;43(20):7728-33. doi: 10.1021/es901385t.

PMID:
19921886
9.

Genetic and infectious prion diseases.

Prusiner SB.

Arch Neurol. 1993 Nov;50(11):1129-53. Review.

PMID:
8105771
10.

Prions and prion diseases: fundamentals and mechanistic details.

Ryou C.

J Microbiol Biotechnol. 2007 Jul;17(7):1059-70. Review.

11.

Prion interaction with the 37-kDa/67-kDa laminin receptor on enterocytes as a cellular model for intestinal uptake of prions.

Kolodziejczak D, Da Costa Dias B, Zuber C, Jovanovic K, Omar A, Beck J, Vana K, Mbazima V, Richt J, Brenig B, Weiss SF.

J Mol Biol. 2010 Sep 17;402(2):293-300. doi: 10.1016/j.jmb.2010.06.055. Epub 2010 Jul 13.

PMID:
20603132
12.

Prion disease: a deadly disease for protein misfolding.

Chakraborty C, Nandi S, Jana S.

Curr Pharm Biotechnol. 2005 Apr;6(2):167-77. Review.

PMID:
15853695
13.

Immunoaffinity purification and neutralization of scrapie prions.

Gabizon R, McKinley MP, Groth D, Westaway D, DeArmond SJ, Carlson GA, Prusiner SB.

Prog Clin Biol Res. 1989;317:583-600. Review.

PMID:
2574871
14.

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
15.

Prions of ruminants show distinct splenotropisms in an ovine transgenic mouse model.

Baron T, Bencsik A, Morignat E.

PLoS One. 2010 Apr 26;5(4):e10310. doi: 10.1371/journal.pone.0010310.

16.

Antiprion properties of prion protein-derived cell-penetrating peptides.

Löfgren K, Wahlström A, Lundberg P, Langel U, Gräslund A, Bedecs K.

FASEB J. 2008 Jul;22(7):2177-84. doi: 10.1096/fj.07-099549. Epub 2008 Feb 22.

PMID:
18296502
17.

Experimental approaches to TSE prevention via inhibition of prion formation.

Politopoulou G.

Protein Pept Lett. 2004 Jun;11(3):249-55. Review.

PMID:
15182226
18.

Prion diseases of the central nervous system.

Prusiner SB, DeArmond SJ.

Monogr Pathol. 1990;(32):86-122. Review.

PMID:
2192281
19.

Prion biology relevant to bovine spongiform encephalopathy.

Novakofski J, Brewer MS, Mateus-Pinilla N, Killefer J, McCusker RH.

J Anim Sci. 2005 Jun;83(6):1455-76. Review.

20.

Transmission of elk and deer prions to transgenic mice.

Tamgüney G, Giles K, Bouzamondo-Bernstein E, Bosque PJ, Miller MW, Safar J, DeArmond SJ, Prusiner SB.

J Virol. 2006 Sep;80(18):9104-14.

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