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Brain Pathology (Zurich, Switzerland)|September 30, 2010
Atypical prion protein conformation in familial prion disease with PRNP P105T mutationMagdalini Polymenidou, Stefan Prokop, Hans H Jung, et al.Proceedings of the National Academy of Sciences of the United States of America|January 17, 2002
Lymph nodal prion replication and neuroinvasion in mice devoid of follicular dendritic cellsMarco Prinz, Fabio Montrasio, Michael A Klein, et al.Cell|April 8, 2003
Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion diseasePhilipp Meier, Nicolas Genoud, Marco Prinz, et al.Human Molecular Genetics|July 1, 2005
The prion gene is associated with human long-term memoryAndreas Papassotiropoulos, M Axel Wollmer, Adriano Aguzzi, et al.The American Journal of Pathology|March 5, 2013
Efficient amyloid A clearance in the absence of immunoglobulins and complement factorsJana Sponarova, Mario Nuvolone, Charlotte Whicher, et al.Vaccine|April 22, 2008
Canine MDCK cell lines are refractory to infection with human and mouse prionsMagdalini Polymenidou, Heidi Trusheim, Lena Stallmach, et al.EMBO Molecular Medicine|July 29, 2010
Prion protein and Abeta-related synaptic toxicity impairmentAnna Maria Calella, Mélissa Farinelli, Mario Nuvolone, et al.BMC Public Health|January 16, 2009
A case-control study of sporadic Creutzfeldt-Jakob disease in Switzerland: analysis of potential risk factors with regard to an increased CJD incidence in the years 2001-2004Jessica Ruegger, Katharina Stoeck, Lorenz Amsler, et al.Plos One|February 18, 2010
Unexpected tolerance of alpha-cleavage of the prion protein to sequence variationsJosé B Oliveira-Martins, Sei-ichi Yusa, Anna Maria Calella, et al.The American Journal of Pathology|December 26, 2009
Structural typing of systemic amyloidoses by luminescent-conjugated polymer spectroscopyK Peter R Nilsson, Kristian Ikenberg, Andreas Aslund, et al.Pageof 57