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Results: 1 to 20 of 11692

1.

Lesion of the Olfactory Epithelium Accelerates Prion Neuroinvasion and Disease Onset when Prion Replication Is Restricted to Neurons.

Crowell J, Wiley JA, Bessen RA.

PLoS One. 2015 Mar 30;10(3):e0119863. doi: 10.1371/journal.pone.0119863. eCollection 2015.

PMID:
25822718
2.

Proteinase K and the structure of PrPSc: the good, the bad and the ugly.

Silva CJ, Vázquez-Fernández E, Onisko B, Requena JR.

Virus Res. 2015 Mar 24. pii: S0168-1702(15)00126-4. doi: 10.1016/j.virusres.2015.03.008. [Epub ahead of print] Review.

PMID:
25816779
3.

Increased Infectivity of Anchorless Mouse Scrapie Prions in Transgenic Mice Overexpressing Human Prion Protein.

Race B, Phillips K, Meade-White K, Striebel J, Chesebro B.

J Virol. 2015 Mar 25. pii: JVI.00362-15. [Epub ahead of print]

PMID:
25810548
4.

Structural Studies of Truncated Forms of the Prion Protein PrP.

Wan W, Wille H, Stöhr J, Kendall A, Bian W, McDonald M, Tiggelaar S, Watts JC, Prusiner SB, Stubbs G.

Biophys J. 2015 Mar 24;108(6):1548-54. doi: 10.1016/j.bpj.2015.01.008.

PMID:
25809267
5.

Correction: A Bovine Cell Line That Can Be Infected by Natural Sheep Scrapie Prions.

PLOS ONE Staff.

PLoS One. 2015 Mar 25;10(3):e0121881. doi: 10.1371/journal.pone.0121881. eCollection 2015.

6.

Detection of exosomal prions in blood by immunochemistry techniques.

Properzi F, Logozzi M, Abdel-Haq H, Federici C, Lugini L, Azzarito T, Cristofaro I, di Sevo D, Ferroni E, Cardone F, Venditti M, Colone M, Comoy E, Durand V, Fais S, Pocchiari M.

J Gen Virol. 2015 Mar 24. pii: vir.0.000117. doi: 10.1099/vir.0.000117. [Epub ahead of print]

PMID:
25805411
7.

Madness and Memory: The Discovery of Prions-A New Biological Principle of Diseaseby Stanley B. Prusiner. New Haven, Conn., Yale University Press, 2014, 344 pp., $30.00.

Lopez O.

Am J Psychiatry. 2014 Nov 1;171(11):1226-7. doi: 10.1176/appi.ajp.2014.14070825. No abstract available.

PMID:
25756641
8.

Methylphenidate prolongs symptom-free period of experimental prion disease in mice.

Nissan I, Gahali-Sass I, Rouvinski A, Makedonski K, Taraboulos A, Tal Y.

J Neurol Sci. 2015 Feb 28. pii: S0022-510X(15)00107-0. doi: 10.1016/j.jns.2015.02.040. [Epub ahead of print] No abstract available.

PMID:
25748967
9.

Predicting the aggregation propensity of prion sequences.

Espargaró A, Busquets MA, Estelrich J, Sabate R.

Virus Res. 2015 Mar 6. pii: S0168-1702(15)00119-7. doi: 10.1016/j.virusres.2015.03.001. [Epub ahead of print]

PMID:
25747492
10.

New insights into structural determinants of prion protein folding and stability.

Benetti F, Legname G.

Prion. 2015 Mar 6:0. [Epub ahead of print]

PMID:
25746597
11.

Invasive procedures in Parkinson's disease: Let's be aware we are dealing with prion-like proteins.

Cersosimo MG.

J Neurol Sci. 2015 Feb 26. pii: S0022-510X(15)00100-8. doi: 10.1016/j.jns.2015.02.033. [Epub ahead of print] No abstract available.

PMID:
25743225
12.

Legal but lethal: functional protein aggregation at the verge of toxicity.

Falsone A, Falsone SF.

Front Cell Neurosci. 2015 Feb 18;9:45. doi: 10.3389/fncel.2015.00045. eCollection 2015. Review.

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Prion infections and anti-PrP antibodies trigger converging neurotoxic pathways.

Herrmann US, Sonati T, Falsig J, Reimann RR, Dametto P, O'Connor T, Li B, Lau A, Hornemann S, Sorce S, Wagner U, Sanoudou D, Aguzzi A.

PLoS Pathog. 2015 Feb 24;11(2):e1004662. doi: 10.1371/journal.ppat.1004662. eCollection 2015 Feb.

16.

Emerging zoonotic viral diseases.

Wang LF, Crameri G.

Rev Sci Tech. 2014 Aug;33(2):569-81.

PMID:
25707184
17.

Human prion protein sequence elements impede cross-species chronic wasting disease transmission.

Kurt TD, Jiang L, Fernández-Borges N, Bett C, Liu J, Yang T, Spraker TR, Castilla J, Eisenberg D, Kong Q, Sigurdson CJ.

J Clin Invest. 2015 Feb 23. pii: 79408. doi: 10.1172/JCI79408. [Epub ahead of print]

PMID:
25705888
18.

Extracellular vesicles - Their role in the packaging and spread of misfolded proteins associated with neurodegenerative diseases.

Coleman BM, Hill AF.

Semin Cell Dev Biol. 2015 Feb 20. pii: S1084-9521(15)00034-8. doi: 10.1016/j.semcdb.2015.02.007. [Epub ahead of print] Review.

PMID:
25704308
19.

Glycosaminoglycan sulfation determines the biochemical properties of prion protein aggregates.

Ellett LJ, Coleman BM, Shambrook MC, Johanssen VA, Collins SJ, Masters CL, Hill AF, Lawson VA.

Glycobiology. 2015 Feb 20. pii: cwv014. [Epub ahead of print]

PMID:
25701659
20.

From molecule to molecule and cell to cell: Prion-like mechanisms in amyotrophic lateral sclerosis.

Grad LI, Fernando SM, Cashman NR.

Neurobiol Dis. 2015 Feb 17. pii: S0969-9961(15)00029-7. doi: 10.1016/j.nbd.2015.02.009. [Epub ahead of print] Review.

PMID:
25701498
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