Cargando…
In Vitro and In Vivo Neurotoxicity of Prion Protein Oligomers
The mechanisms underlying prion-linked neurodegeneration remain to be elucidated, despite several recent advances in this field. Herein, we show that soluble, low molecular weight oligomers of the full-length prion protein (PrP), which possess characteristics of PrP to PrPsc conversion intermediates...
Autores principales: | Simoneau, Steve, Rezaei, Human, Salès, Nicole, Kaiser-Schulz, Gunnar, Lefebvre-Roque, Maxime, Vidal, Catherine, Fournier, Jean-Guy, Comte, Julien, Wopfner, Franziska, Grosclaude, Jeanne, Schätzl, Hermann, Lasmézas, Corinne Ida |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1959381/ https://www.ncbi.nlm.nih.gov/pubmed/17784787 http://dx.doi.org/10.1371/journal.ppat.0030125 |
Ejemplares similares
-
Prion Strain Discrimination Based on Rapid In Vivo Amplification and Analysis by the Cell Panel Assay
por: Karapetyan, Yervand Eduard, et al.
Publicado: (2009) -
An N-terminal Fragment of the Prion Protein Binds to Amyloid-β Oligomers and Inhibits Their Neurotoxicity in Vivo
por: Fluharty, Brian R., et al.
Publicado: (2013) -
Tau Oligomers Neurotoxicity
por: Niewiadomska, Grazyna, et al.
Publicado: (2021) -
Biochemical insight into the prion protein family
por: Ciric, Danica, et al.
Publicado: (2015) -
Reversibility of Aβ oligomer neurotoxicity
por: Araki, Wataru
Publicado: (2017)