Cellular prion protein neuroprotective function: Implications in prion diseasesROUCOU, Xavier; LEBLANC, Andréa C.Journal of molecular medicine (Berlin. Print). 2005, Vol 83, Num 1, pp 3-11, issn 0946-2716, 9 p.Article

Interactions of prion proteins with soilLEITA, Liviana; FORNASIER, Flavio; DE NOBILI, Maria et al.Soil biology & biochemistry. 2006, Vol 38, Num 7, pp 1638-1644, issn 0038-0717, 7 p.Article

Polymorphism of PRNP codons in the normal Icelandic populationGEORGSSON, G; TRYGGVASON, T; JONASDOTTIR, A. D et al.Acta neurologica scandinavica. 2006, Vol 113, Num 6, pp 419-425, issn 0001-6314, 7 p.Article

Quantitative analysis of residual protein contamination on reprocessed surgical instrumentsBAXTER, R. L; BAXTER, H. C; CAMPBELL, G. A et al.The Journal of hospital infection. 2006, Vol 63, Num 4, pp 439-444, issn 0195-6701, 6 p.Article

The cellular prion protein (PrP^C) prevents apoptotic neuronal cell death and mitochondrial dysfunction induced by serum deprivationKIM, Boe-Hyun; LEE, Hyoung-Gon; CHOI, Jin-Kyu et al.Molecular brain research. 2004, Vol 124, Num 1, pp 40-50, issn 0169-328X, 11 p.Article

Structure and assembly properties of the yeast prion Ure2pBOUSSET, Luc; THUAL, Carine; BELRHALI, Hassan et al.Comptes rendus. Biologies. 2002, Vol 325, Num 1, pp 3-8, issn 1631-0691Article

Genetic prion disease : the EUROCJD experienceKOVACS, Gabor G; PUOPOLO, Maria; DELASNERIE-LAUPRETRE, Nicole et al.Human genetics. 2005, Vol 118, Num 2, pp 166-174, issn 0340-6717, 9 p.Article

Prion diseasesKNIGHT, R. S. G; WILL, R. G.Neurology in practice. 2004, Vol 75, pp i36-i42, issn 1473-7086, SUP1Article

Widespread prehistoric human cannibalism: easier to swallow?STONEKING, Mark.Trends in ecology & evolution (Amsterdam). 2003, Vol 18, Num 10, pp 489-490, issn 0169-5347, 2 p.Article

Gerstmann-Sträussler-Scheinker disease with P102L-V129 mutation: a case with psychiatric manifestations at onsetBIANCA, Marco; BIANCA, Sebastiano; VECCHIO, Ignazio et al.Annales de génétique (Paris). 2003, Vol 46, Num 4, pp 467-469, issn 0003-3995, 3 p.Article

Production of Prnp^-/-goats by gene targeting in adult fibroblastsCAIHONG ZHU; BEI LI; GUOHUA YU et al.Transgenic research. 2009, Vol 18, Num 2, pp 163-171, issn 0962-8819, 9 p.Article

Early age of onset in fatal familial insomnia: Two novel cases and review of the literatureHARDER, A; GREGOR, A; KUHLMANN, T et al.Journal of neurology. 2004, Vol 251, Num 6, pp 715-724, issn 0340-5354, 10 p.Article

Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted diseasePARCHI, Piero; CESCATTI, Maura; NOTARI, Silvio et al.Brain. 2010, Vol 133, pp 3030-3042, issn 0006-8950, 13 p., 10Article

The Prion's Elusive Reason for BeingAGUZZI, Adriano; BAUMANN, Frank; BREMER, Juliane et al.Annual review of neuroscience. 2008, Vol 31, pp 439-477, issn 0147-006X, 39 p.Article

Population-level retrospective study of neurologically expressed disorders in ruminants before the onset of Bovine Spongiform Encephalopathy (BSE) in Belgium, a BSE risk III countrySAEGERMAN, C; BERKVENS, D; DELUYKER, H et al.Journal of clinical microbiology (Print). 2005, Vol 43, Num 2, pp 862-869, issn 0095-1137, 8 p.Article

Pathogenèse des maladies à prions : Maladies à prionsLACROUX, Caroline; ANDREOLETTI, Olivier.Biofutur (Puteaux). 2009, Num 302, pp 40-43, issn 0294-3506, 4 p.Article

Prions and prion diseases : Fundamentals and mechanistic detailsRYOU, Chongsuk.Journal of microbiology and biotechnology. 2007, Vol 17, Num 7, pp 1059-1070, issn 1017-7825, 12 p.Article

Preimplantation exclusion of embryos at risk for prion diseasesMEINER, V; WEINBERG, N; SAFRAN, A et al.Neurology. 2006, Vol 66, Num 4, pp 607-608, issn 0028-3878, 2 p.Article

Human prion diseases : Molecular and clinical aspectsGLATZEL, Markus; STOECK, Katharina; SEEGER, Harald et al.Archives of neurology (Chicago). 2005, Vol 62, Num 4, pp 545-552, issn 0003-9942, 8 p.Article

Accelerated prion disease in the absence of interleukin-10THACKRAY, Alana M; MCKENZIE, Andrew N; KLEIN, Michael A et al.Journal of virology. 2004, Vol 78, Num 24, pp 13697-13707, issn 0022-538X, 11 p.Article

Past, present and future of bovine spongiform encephalopathy in FranceCALAVAS, D; DUCROT, C; BARON, T. G. M et al.Current Topics in Microbiology and Immunology. 2004, Vol 284, pp 51-63, issn 0070-217X, 13 p.Article

Some considerations on the kinetics of pathogenic prions formationBOTRE, Claudio; BOTRE, Francesco; MAZZEI, Franco et al.Annali dell' Istituto superiore di sanità. 2002, Vol 38, Num 2, pp 195-198, issn 0021-2571Article

Avis et recommandations sur les encéphalopathies spongiformes subaiguès transmissibles. Septembre 1999-juin 20012001, 504 p.Book

No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob diseaseCOLLINS, Steven J; SCHUUR, Maaike; VAN DUIJN, Cornelia M et al.Neuroscience letters. 2010, Vol 472, Num 1, pp 16-18, issn 0304-3940, 3 p.Article

Loss of Perineuronal Net in ME7 Prion DiseaseFRANKLIN, Sarah L; LOVE, Seth; GREENE, J. Richard T et al.Journal of neuropathology and experimental neurology. 2008, Vol 67, Num 3, pp 189-199, issn 0022-3069, 11 p.Article