Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Adriano Aguzzi

Showing results (161-170 of 384) with videos related to

Pageof 39
Sort By:
Plos Pathogens|January 29, 2016
Differential Toxicity of Antibodies to the Prion ProteinRegina R Reimann, Tiziana Sonati, Simone Hornemann, et al.
EMBO Molecular Medicine|July 22, 2021
Loss of PIKfyve drives the spongiform degeneration in prion diseasesAsvin K K Lakkaraju, Karl Frontzek, Emina Lemes, et al.
Stroke|March 16, 2021
Observation of Collagen-Containing Lesions After Hematoma Resolution in Intracerebral HemorrhageChristopher J Love, Daniel Kirschenbaum, Magdy Selim, 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.
Pageof 39

Showing results (161-170 of 384) with videos related to

Sort By:
Pageof 39
Plos Pathogens|January 29, 2016
Differential Toxicity of Antibodies to the Prion ProteinRegina R Reimann, Tiziana Sonati, Simone Hornemann, et al.
EMBO Molecular Medicine|July 22, 2021
Loss of PIKfyve drives the spongiform degeneration in prion diseasesAsvin K K Lakkaraju, Karl Frontzek, Emina Lemes, et al.
Stroke|March 16, 2021
Observation of Collagen-Containing Lesions After Hematoma Resolution in Intracerebral HemorrhageChristopher J Love, Daniel Kirschenbaum, Magdy Selim, 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.
Pageof 39