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Nature Chemical Biology|January 16, 2023
A structural basis for prion strain diversitySzymon W Manka, Adam Wenborn, Jemma Betts, et al.
The Journal of General Virology|August 16, 2005
PrP glycoforms are associated in a strain-specific ratio in native PrPScAzadeh Khalili-Shirazi, Linda Summers, Jacqueline Linehan, et al.
Brain : a Journal of Neurology|June 25, 2003
Regional heterogeneity of cellular prion protein isoforms in the mouse brainVincent Beringue, Gary Mallinson, Maria Kaisar, et al.
Scientific Reports|June 10, 2022
A high-content neuron imaging assay demonstrates inhibition of prion disease-associated neurotoxicity by an anti-prion protein antibodyMadeleine Reilly, Iryna Benilova, Azadeh Khalili-Shirazi, et al.
The Biochemical Journal|August 8, 2008
Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysinSabrina Cronier, Nathalie Gros, M Howard Tattum, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 2018
Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease progressionAndrew Geoffrey Bourne Thompson, Connie Luk, Amanda J Heslegrave, et al.
Journal of Alzheimer'S Disease : JAD|April 13, 2013
The presenilin 1 P264L mutation presenting as non-fluent/agrammatic primary progressive aphasiaColin J Mahoney, Laura E Downey, Jon Beck, et al.
Nature|March 7, 2003
Monoclonal antibodies inhibit prion replication and delay the development of prion diseaseAnthony R White, Perry Enever, Mourad Tayebi, et al.
The Journal of Biological Chemistry|September 15, 2005
Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosisMark Kristiansen, Marcus J Messenger, Peter-Christian Klöhn, et al.
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