Cargando…
Molecular Interactions between Prions as Seeds and Recombinant Prion Proteins as Substrates Resemble the Biological Interspecies Barrier In Vitro
Prion diseases like Creutzfeldt-Jakob disease in humans, Scrapie in sheep or bovine spongiform encephalopathy are fatal neurodegenerative diseases, which can be of sporadic, genetic, or infectious origin. Prion diseases are transmissible between different species, however, with a variable species ba...
Autores principales: | Panza, Giannantonio, Luers, Lars, Stöhr, Jan, Nagel-Steger, Luitgard, Weiβ, Jürgen, Riesner, Detlev, Willbold, Dieter, Birkmann, Eva |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000319/ https://www.ncbi.nlm.nih.gov/pubmed/21151607 http://dx.doi.org/10.1371/journal.pone.0014283 |
Ejemplares similares
-
Seeded Fibrillation as Molecular Basis of the Species Barrier in Human Prion Diseases
por: Luers, Lars, et al.
Publicado: (2013) -
Detection of Prion Protein Particles in Blood Plasma of Scrapie Infected Sheep
por: Bannach, Oliver, et al.
Publicado: (2012) -
Met/Val129 polymorphism of the full-length human prion protein dictates distinct pathways of amyloid formation
por: Pauly, Thomas, et al.
Publicado: (2022) -
Efficient interspecies transmission of synthetic prions
por: Block, Alyssa J., et al.
Publicado: (2021) -
Influence of Interspecies Transmission of Atypical Bovine Spongiform Encephalopathy Prions to Hamsters on Prion Characteristics
por: Miyazawa, Kohtaro, et al.
Publicado: (2020)