Serene L. Wohlgemuth
Edmonton, AB, Canada
Last Updated: 09/26/2026
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Found 18 publications
Disruption of the c-terminal serine protease domain of Fam111a does not alter calcium homeostasis in mice.
Journal: Physiological reports
Published: December 31, 2023
Expression of progerin enhances disease-related endpoints in a tau seeding reporter cell system.
Journal: GeroScience
Published: December 19, 2023
Beta-endoproteolysis of the cellular prion protein by dipeptidyl peptidase-4 and fibroblast activation protein.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 27, 2022
Investigating CRISPR/Cas9 gene drive for production of disease-preventing prion gene alleles.
Journal: PloS one
Published: March 27, 2022
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
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
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
Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation.
Journal: EMBO molecular medicine
Published: February 10, 2015
Last Updated: 09/26/2026