Associated Papers
Y225A induces long-range conformational changes in human prion protein that are protective in Drosophila.
Myers RR et al.
The Journal of Biological Chemistry, 2023
Drosophila melanogaster as a model to study autophagy in neurodegenerative diseases induced by proteinopathies.
Santarelli S et al.
Frontiers in Neuroscience, 2023
Intrinsic determinants of prion protein neurotoxicity in Drosophila: from sequence to (dys)function.
Cembran A et al.
Frontiers in Molecular Neuroscience, 2023
New Drosophila models to uncover the intrinsic and extrinsic factors that mediate the toxicity of the human prion protein.
Myers RR et al.
Disease Models & Mechanisms, 2022
Insight From Animals Resistant to Prion Diseases: Deciphering the Genotype - Morphotype - Phenotype Code for the Prion Protein.
Myers R et al.
Frontiers in Cellular Neuroscience, 2020
A proposed mechanism for the promotion of prion conversion involving a strictly conserved tyrosine residue in the β2-α2 loop of PrPC.
Kurt TD et al.
The Journal of Biological Chemistry, 2014
N-terminal helix-cap in α-helix 2 modulates β-state misfolding in rabbit and hamster prion proteins.
Sweeting B et al.
Plos One, 2013
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