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International Journal of Molecular Sciences|January 24, 2019
Investigating the Molecular Basis of the Aggregation Propensity of the Pathological D76N Mutant of Beta-2 Microglobulin: Role of the Denatured StateLorenzo Visconti, Francesca Malagrinò, Luca Broggini, et al.Antioxidants (Basel, Switzerland)|July 2, 2021
Profiling Dopamine-Induced Oxidized Proteoforms of β-synuclein by Top-Down Mass SpectrometryArianna Luise, Elena De Cecco, Erika Ponzini, et al.Biochemistry|July 14, 2012
Effects of the pathological Q212P mutation on human prion protein non-octarepeat copper-binding sitePaola D'Angelo, Stefano Della Longa, Alessandro Arcovito, et al.The Biochemical Journal|November 13, 2008
Development of antibody fragments for immunotherapy of prion diseasesVincenza Campana, Lorena Zentilin, Ilaria Mirabile, et al.Journal of Chemical Theory and Computation|December 1, 2015
Docking Ligands on Protein Surfaces: The Case Study of Prion ProteinAgata Kranjc, Salvatore Bongarzone, Giulia Rossetti, et al.Science (New York, N.Y.)|August 3, 2004
Synthetic mammalian prionsGiuseppe Legname, Ilia V Baskakov, Hoang-Oanh B Nguyen, et al.Biomedicines|August 6, 2021
Animal Models of Autosomal Recessive ParkinsonismGuendalina Bastioli, Maria Regoni, Federico Cazzaniga, et al.Annals of Clinical and Translational Neurology|October 10, 2023
Detection of prions in the urine of patients affected by sporadic Creutzfeldt-Jakob diseaseSandra Pritzkow, Frank Ramirez, Adam Lyon, et al.Scientific Reports|March 28, 2019
PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission studyIgnazio Cali, Jody Lavrich, Fabio Moda, et al.Nanoscale|February 28, 2020
Iron-mediated interaction of alpha synuclein with lipid raft model membranesFabio Perissinotto, Chiaramaria Stani, Elena De Cecco, et al.Pageof 24