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The Journal of Biological Chemistry|October 2, 2019
Leveraging a large microbial strain collection for natural product discoveryAndrew D Steele, Christiana N Teijaro, Dong Yang, et al.The EMBO Journal|July 12, 2002
Absence of the prion protein homologue Doppel causes male sterilityAxel Behrens, Nicolas Genoud, Heike Naumann, et al.Journal of Neurochemistry|May 13, 2020
The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cellsElena De Cecco, Luigi Celauro, Silvia Vanni, et al.Prion|December 5, 2015
Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein geneKarl Frontzek, Rita Moos, Elke Schaper, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 13, 2005
Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPCIvan Radovanovic, Nathalie Braun, Olivier T Giger, et al.Plos Pathogens|March 26, 2011
The strain-encoded relationship between PrP replication, stability and processing in neurons is predictive of the incubation period of diseaseJacob I Ayers, Charles R Schutt, Ronald A Shikiya, et al.Oncogene|April 6, 2004
IL-6 is required for glioma development in a mouse modelJakob Weissenberger, Sébastien Loeffler, Andreas Kappeler, et al.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.Pageof 41