Human cerebral organoids as a therapeutic drug screening model for Creutzfeldt–Jakob disease

Creutzfeldt–Jakob Disease (CJD) is a fatal, currently incurable, neurodegenerative disease. The search for candidate treatments would be greatly facilitated by the availability of human cell-based models of prion disease. Recently, an induced pluripotent stem cell derived human cerebral organoid mod...

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Detalles Bibliográficos
Autores principales: Groveman, Bradley R., Ferreira, Natalia C., Foliaki, Simote T., Walters, Ryan O., Winkler, Clayton W., Race, Brent, Hughson, Andrew G., Zanusso, Gianluigi, Haigh, Cathryn L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943797/
https://www.ncbi.nlm.nih.gov/pubmed/33727594
http://dx.doi.org/10.1038/s41598-021-84689-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943797/
https://www.ncbi.nlm.nih.gov/pubmed/33727594
http://dx.doi.org/10.1038/s41598-021-84689-6

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