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Elife|September 22, 2020
Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neuronsClaudia Scheckel, Marigona Imeri, Petra Schwarz, et al.Trends in Microbiology|March 26, 2004
Variant Creutzfeldt-jakob disease: between lymphoid organs and brainMarkus Glatzel, Olivier Giger, Harald Seeger, et al.The New England Journal of Medicine|November 7, 2003
Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob diseaseMarkus Glatzel, Eugenio Abela, Manuela Maissen, et al.Journal of Molecular Medicine (Berlin, Germany)|March 24, 2021
The role of macrophage scavenger receptor 1 (Msr1) in prion pathogenesisBei Li, Meiling Chen, Adriano Aguzzi, et al.Journal of Mass Spectrometry : JMS|March 14, 2009
Hydrogen/deuterium exchange mass spectrometry identifies two highly protected regions in recombinant full-length prion protein amyloid fibrilsAlexis Nazabal, Simone Hornemann, Adriano Aguzzi, et al.Science (New York, N.Y.)|January 12, 2013
Microglia: scapegoat, saboteur, or something else?Adriano Aguzzi, Ben A Barres, Mariko L BennettJournal of Molecular Neuroscience : MN|May 6, 2004
Current concepts and controversies in prion immunopathologyMathias Heikenwalder, Marco Prinz, Frank L Heppner, et al.Brain Research|March 27, 2012
Misregulated RNA processing in amyotrophic lateral sclerosisMagdalini Polymenidou, Clotilde Lagier-Tourenne, Kasey R Hutt, et al.Elife|December 18, 2024
Antimicrobial activity of iron-depriving pyoverdines against human opportunistic pathogensVera Vollenweider, Karoline Rehm, Clara Chepkirui, et al.BMC Infectious Diseases|October 9, 2002
A short purification process for quantitative isolation of PrPSc from naturally occurring and experimental transmissible spongiform encephalopathiesMagdalini Polymenidou, Susan Verghese-Nikolakaki, Martin Groschup, et al.Pageof 39