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Annals of Neurology|January 6, 2004
Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscleGabor G Kovacs, Elisabeth Lindeck-Pozza, Leila Chimelli, et al.
Plos One|November 12, 2020
Soluble dimeric prion protein ligand activates Adgrg6 receptor but does not rescue early signs of demyelination in PrP-deficient miceAnna Henzi, Assunta Senatore, Asvin K K Lakkaraju, et al.
European Neurology|January 21, 2012
Phenotypic variation of autosomal-dominant corticobasal degenerationHans H Jung, Juliane Bremer, Johannes Streffer, et al.
European Journal of Immunology|July 15, 2006
Expression of lymphotoxin beta governs immunity at two distinct levelsTobias Junt, Alexei V Tumanov, Nicola Harris, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 17, 2014
Prion transmission prevented by modifying the β2-α2 loop structure of host PrPCTimothy D Kurt, Cyrus Bett, Natalia Fernández-Borges, et al.
Nature Communications|November 13, 2020
Developmental divergence of sensory stimulus representation in cortical interneuronsRahel Kastli, Rasmus Vighagen, Alexander van der Bourg, et al.
Msphere|December 5, 2017
Relative Impact of Complement Receptors CD21/35 (Cr2/1) on Scrapie Pathogenesis in MiceSarah J Kane, Eric Swanson, Elizabeth O Gordon, et al.
Plos One|June 26, 2018
Food anticipatory activity on a calorie-restricted diet is independent of Sirt1Dina R Assali, Cynthia T Hsu, Keith M Gunapala, et al.
The Lancet. Neurology|November 26, 2003
Human prion diseases: epidemiology and integrated risk assessmentMarkus Glatzel, Peter M Ott, Thomas Linder, et al.
FEBS Letters|July 19, 2005
PrP(106-126) activates neuronal intracellular kinases and Egr1 synthesis through activation of NADPH-oxidase independently of PrPcRosalina Gavín, Nathalie Braun, Oriol Nicolas, et al.
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