Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 201

1.

The prion's elusive reason for being.

Aguzzi A, Baumann F, Bremer J.

Annu Rev Neurosci. 2008;31:439-77. doi: 10.1146/annurev.neuro.31.060407.125620. Review.

PMID:
18558863
2.

Prion proteins: a biological role beyond prion diseases.

Hu W, Rosenberg RN, Stüve O.

Acta Neurol Scand. 2007 Aug;116(2):75-82. Review.

PMID:
17661791
3.

Cellular prion protein co-localizes with nAChR beta4 subunit in brain and gastrointestinal tract.

Petrakis S, Irinopoulou T, Panagiotidis CH, Engelstein R, Lindstrom J, Orr-Urtreger A, Gabizon R, Grigoriadis N, Sklaviadis T.

Eur J Neurosci. 2008 Feb;27(3):612-20. doi: 10.1111/j.1460-9568.2008.06037.x. Erratum in: Eur J Neurosci. 2008 Apr;27(8):2212.

PMID:
18279314
4.
5.

Prion protein: orchestrating neurotrophic activities.

Martins VR, Beraldo FH, Hajj GN, Lopes MH, Lee KS, Prado MA, Linden R.

Curr Issues Mol Biol. 2010;12(2):63-86. Epub 2009 Sep 18. Review.

6.

Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality.

Coleman BM, Harrison CF, Guo B, Masters CL, Barnham KJ, Lawson VA, Hill AF.

J Virol. 2014 Mar;88(5):2690-703. doi: 10.1128/JVI.02720-13. Epub 2013 Dec 18.

7.

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.

8.

Prion proteins: physiological functions and role in neurological disorders.

Hu W, Kieseier B, Frohman E, Eagar TN, Rosenberg RN, Hartung HP, Stüve O.

J Neurol Sci. 2008 Jan 15;264(1-2):1-8. Epub 2007 Aug 17. Review.

PMID:
17707411
9.

The role of PrP in health and disease.

Flechsig E, Weissmann C.

Curr Mol Med. 2004 Jun;4(4):337-53. Review.

PMID:
15354865
10.

[Mechanisms of neuroinvasion by prions: molecular principles and present state of research].

Brandner S, Klein MA, Aguzzi A.

Schweiz Med Wochenschr. 2000 Mar 25;130(12):435-42. Review. German.

PMID:
10780058
11.

Prion protein self-interactions: a gateway to novel therapeutic strategies?

Rigter A, Langeveld JP, van Zijderveld FG, Bossers A.

Vaccine. 2010 Nov 16;28(49):7810-23. doi: 10.1016/j.vaccine.2010.09.012. Epub 2010 Oct 20. Review.

PMID:
20932496
12.

Evolving views in prion glycosylation: functional and pathological implications.

Ermonval M, Mouillet-Richard S, Codogno P, Kellermann O, Botti J.

Biochimie. 2003 Jan-Feb;85(1-2):33-45. Review.

PMID:
12765773
13.

Molecular clues to pathogenesis in prion diseases.

Laurent M, Johannin G.

Histol Histopathol. 1997 Apr;12(2):583-94. Review.

PMID:
9151145
14.

Transmissible spongiform encephalopathies.

Liemann S, Glockshuber R.

Biochem Biophys Res Commun. 1998 Sep 18;250(2):187-93. Review.

PMID:
9753605
15.

Transmissible and genetic prion diseases share a common pathway of neurodegeneration.

Hegde RS, Tremblay P, Groth D, DeArmond SJ, Prusiner SB, Lingappa VR.

Nature. 1999 Dec 16;402(6763):822-6.

PMID:
10617204
16.

New insights into prion structure and toxicity.

Harris DA, True HL.

Neuron. 2006 May 4;50(3):353-7. Review.

17.

[Mechanisms of prion transmission].

Sakaguchi S.

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

PMID:
17695274
18.

Prions: pathogenesis and reverse genetics.

Aguzzi A, Klein MA, Montrasio F, Pekarik V, Brandner S, Furukawa H, Käser P, Röckl C, Glatzel M.

Ann N Y Acad Sci. 2000;920:140-57. Review.

PMID:
11193143
20.

Supplemental Content

Support Center