Associated Papers
The First Genetic Characterization of the SPRN Gene in Pekin Ducks (Anas platyrhynchos domesticus).
Nguyen TT et al.
Animals : an Open Access Journal From Mdpi, 2024
Arg177 and Asp159 from dog prion protein slow liquid-liquid phase separation and inhibit amyloid formation of human prion protein.
Li XN 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 Single Amino Acid Substitution, Found in Mammals with Low Susceptibility to Prion Diseases, Delays Propagation of Two Prion Strains in Highly Susceptible Transgenic Mouse Models.
Otero A et al.
Molecular Neurobiology, 2019
D159 and S167 are protective residues in the prion protein from dog and horse, two prion-resistant animals.
Sanchez-Garcia J et al.
Neurobiology of Disease, 2018
A single amino acid (Asp159) from the dog prion protein suppresses the toxicity of the mouse prion protein in Drosophila.
Sanchez-Garcia J et al.
Neurobiology of Disease, 2016
Pulling rabbits to reveal the secrets of the prion protein.
Fernandez-Funez P et al.
Communicative & Integrative Biology, 2011
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