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Differential overexpression of SERPINA3 in human prion diseases 1-gen-2017 Vanni, S.Moda, F.Zattoni, M.Bistaffa, E.De Cecco, E.Zanusso, G.Legname, G. +
alpha-Synuclein Amyloids Hijack Prion Protein to Gain Cell Entry, Facilitate Cell-to-Cell Spreading and Block Prion Replication 1-gen-2017 Aulić, SuzanaMasperone, LaraNarkiewicz, JoannaIsopi, ElisaBistaffa, EdoardoPastore, BeatriceDe Cecco, ElenaScaini, DenisZago, PaolaModa, FabioLegname, Giuseppe +
The role of the prion protein in the internalization of α-synuclein amyloids 1-gen-2018 De Cecco, ElenaLegname, Giuseppe
Prion and prion-like protein strains: Deciphering the molecular basis of heterogeneity in neurodegeneration 1-gen-2019 Scialò C.De Cecco E.Legname G. +
Efficient RT-QuIC seeding activity for α-synuclein in olfactory mucosa samples of patients with Parkinson's disease and multiple system atrophy 1-gen-2019 De Cecco E.Narkiewicz J.Salzano G.Legname G. +
Functions of the prion protein in neurodegeneration: a closer look to tau - PrP interaction 31-ott-2019 De Cecco, Elena
The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cells 1-gen-2020 De Cecco, E.Celauro, L.Vanni, S.Grandolfo, M.Legname, G. +
Dynamic molecular exchange and conformational transitions of alpha-synuclein at the nano-bio interface 1-gen-2020 De Cecco, E.Legname, G. +
Iron-mediated interaction of alpha synuclein with lipid raft model membranes 1-gen-2020 De Cecco, E.Scaini, D.Legname, G. +
Profiling dopamine-induced oxidized proteoforms of β-synuclein by top-down mass spectrometry 1-gen-2021 De Cecco, E.Legname, G. +
Gerstmann–Sträussler–Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles 1-gen-2022 De Cecco E.Legname G. +
Different tau fibril types reduce prion level in chronically and de novo infected cells 1-gen-2023 Celauro L.Burato A.Zattoni M.De Cecco E.Fantuz M.Bistaffa E.Moda F.Legname G. +
Mostrati risultati da 1 a 12 di 12
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