Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.
<h4>Objective</h4>The glycoprofile of pathological prion protein (PrP(res)) is widely used as a diagnosis marker in Creutzfeldt-Jakob disease (CJD) and is thought to vary in a strain-specific manner. However, that the same glycoprofile of PrP(res) always accumulates in the whole brain of...
Guardado en:
Autores principales: | Etienne Levavasseur, Isabelle Laffont-Proust, Emilie Morain, Baptiste A Faucheux, Nicolas Privat, Katell Peoc'h, Véronique Sazdovitch, Jean-Philippe Brandel, Jean-Jacques Hauw, Stéphane Haïk |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2008
|
Materias: | |
Acceso en línea: | https://doaj.org/article/7bc2423300c54e9fbbe5a6970abf32ec |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt–Jakob disease prions is strongly seed and substrate dependent
por: Maxime Bélondrade, et al.
Publicado: (2021) -
Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures
por: Hervé Cassard, et al.
Publicado: (2020) -
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients
por: Christina D. Orrù, et al.
Publicado: (2018) -
Prion type 2 selection in sporadic Creutzfeldt–Jakob disease affecting peripheral ganglia
por: Anna Hofmann, et al.
Publicado: (2021) -
Enfermedad por priones, encefalopatía espongiforme humana y enfermedad de Creutzfeldt-Jakob
por: Cartier-Rovirosa,Luis
Publicado: (2019)