Cargando…
Prion pathogenesis is unaltered following down-regulation of SIGN-R1
Prion diseases are infectious neurodegenerative disorders characterised by accumulations of abnormal prion glycoprotein in affected tissues. Following peripheral exposure, many prion strains replicate upon follicular dendritic cells (FDC) in lymphoid tissues before infecting the brain. An intact spl...
Autores principales: | Bradford, Barry M., Brown, Karen L., Mabbott, Neil A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031137/ https://www.ncbi.nlm.nih.gov/pubmed/27522473 http://dx.doi.org/10.1016/j.virol.2016.08.005 |
Ejemplares similares
-
Unaltered intravenous prion disease pathogenesis in the temporary absence of marginal zone B cells
por: Bradford, Barry M., et al.
Publicado: (2019) -
Peripheral prion disease pathogenesis is unaltered in the absence of sialoadhesin (Siglec-1/CD169)
por: Bradford, Barry M, et al.
Publicado: (2014) -
Prion disease pathogenesis in the absence of the commensal microbiota
por: Bradford, Barry M., et al.
Publicado: (2017) -
The Effects of Immune System Modulation on Prion Disease Susceptibility and Pathogenesis
por: Mabbott, Neil A., et al.
Publicado: (2020) -
Oral Prion Disease Pathogenesis Is Impeded in the Specific Absence of CXCR5-Expressing Dendritic Cells
por: Bradford, Barry M., et al.
Publicado: (2017)