Nathalie Daude
Edmonton, AB T6G2R3, Canada
Last Updated: 09/26/2026
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Found 22 publications
Prion protein with a mutant N-terminal octarepeat region undergoes cobalamin-dependent assembly into high-molecular weight complexes.
Journal: The Journal of biological chemistry
Published: December 22, 2021
Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation.
Journal: Acta neuropathologica
Published: January 30, 2021
Quaternary Structure Changes for PrPSc Predate PrPC Downregulation and Neuronal Death During Progression of Experimental Scrapie Disease.
Journal: Molecular neurobiology
Published: March 28, 2020
Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation.
Journal: Acta neuropathologica
Published: November 25, 2019
Proteasomal Inhibition Redirects the PrP-Like Shadoo Protein to the Nucleus.
Journal: Molecular neurobiology
Published: January 17, 2019
Application of high-throughput, capillary-based Western analysis to modulated cleavage of the cellular prion protein.
Journal: The Journal of biological chemistry
Published: October 22, 2018
A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles.
Journal: PLoS pathogens
Published: June 06, 2017
The CNS in inbred transgenic models of 4-repeat Tauopathy develops consistent tau seeding capacity yet focal and diverse patterns of protein deposition.
Journal: Molecular neurodegeneration
Published: May 15, 2017
Last Updated: 09/26/2026