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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...
Enregistré dans:
| Publié dans: | Sci Rep |
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| Auteurs principaux: | , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Nature Publishing Group UK
2021
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7943797/ https://ncbi.nlm.nih.gov/pubmed/33727594 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-84689-6 |
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