Cargando…
Heterozygosity for cervid S138N polymorphism results in subclinical CWD in gene-targeted mice and progressive inhibition of prion conversion
Prions are proteinaceous infectious particles that replicate by structural conversion of the host-encoded cellular prion protein (PrP(C)), causing fatal neurodegenerative diseases in mammals. Species-specific amino acid substitutions (AAS) arising from single nucleotide polymorphisms within the prio...
Autores principales: | Arifin, Maria I., Kaczmarczyk, Lech, Zeng, Doris, Hannaoui, Samia, Lee, Chi, Chang, Sheng Chun, Mitchell, Gordon, McKenzie, Debbie, Beekes, Michael, Jackson, Walker, Gilch, Sabine |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104538/ https://www.ncbi.nlm.nih.gov/pubmed/37014866 http://dx.doi.org/10.1073/pnas.2221060120 |
Ejemplares similares
-
Transmission of cervid prions to humanized mice demonstrates the zoonotic potential of CWD
por: Hannaoui, Samia, et al.
Publicado: (2022) -
Destabilizing polymorphism in cervid prion protein hydrophobic core determines prion conformation and conversion efficiency
por: Hannaoui, Samia, et al.
Publicado: (2017) -
Cervid Prion Protein Polymorphisms: Role in Chronic Wasting Disease Pathogenesis
por: Arifin, Maria Immaculata, et al.
Publicado: (2021) -
Genetic modulation of CWD prion propagation in cervid PrP Drosophila
por: Thackray, Alana M., et al.
Publicado: (2023) -
Shedding and stability of CWD prion seeding activity in cervid feces
por: Tennant, Joanne M., et al.
Publicado: (2020)