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Plos Pathogens|December 4, 2009
Continuous quinacrine treatment results in the formation of drug-resistant prionsSina Ghaemmaghami, Misol Ahn, Pierre Lessard, et al.
European Journal of Medicinal Chemistry|November 16, 2016
Identification of novel fluorescent probes preventing PrPSc replication in prion diseasesLudovica Zaccagnini, Simone Brogi, Margherita Brindisi, et al.
Plos One|July 28, 2010
NMR structure of the human prion protein with the pathological Q212P mutation reveals unique structural featuresGregor Ilc, Gabriele Giachin, Mariusz Jaremko, et al.
Biochemistry|July 22, 2009
Prion proteins with pathogenic and protective mutations show similar structure and dynamicsSung-Hun Bae, Giuseppe Legname, Ana Serban, et al.
ACS Omega|December 3, 2019
Unique Structural Features of Mule Deer Prion Protein Provide Insights into Chronic Wasting DiseaseUrška Slapšak, Giulia Salzano, Gregor Ilc, et al.
Aging Cell|May 10, 2024
Oxidative stress-related cellular aging causes dysfunction of the Kv3.1/KCNC1 channel reverted by melatoninSara Spinelli, Alessia Remigante, Raffaella Liuni, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 16, 2025
Detection of TDP-43 seeds in CSF of presymptomatic and symptomatic genetic FTD/ALSIlaria Linda Dellarole, Vittoria Aprea, Marcella Catania, et al.
Biochemistry|October 9, 2002
Locally disordered conformer of the hamster prion protein: a crucial intermediate to PrPSc?Kazuo Kuwata, Hua Li, Hiroaki Yamada, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 22, 2007
Prion detection by an amyloid seeding assayDavid W Colby, Qiang Zhang, Shuyi Wang, et al.
Science Translational Medicine|December 23, 2016
Detection of prions in blood from patients with variant Creutzfeldt-Jakob diseaseLuis Concha-Marambio, Sandra Pritzkow, Fabio Moda, et al.
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