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Delivering the CRISPR/Cas9 system for engineering gene therapies: Recent cargo and delivery approaches for clinical translation

Clustered Regularly Interspaced Short Palindromic Repeats associated protein 9 (CRISPR/Cas9) has transformed our ability to edit the human genome selectively. This technology has quickly become the most standardized and reproducible gene editing tool available. Catalyzing rapid advances in biomedica...

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Detalles Bibliográficos
Autores principales: Foley, Ruth A., Sims, Ruby A., Duggan, Emily C., Olmedo, Jessica K., Ma, Rachel, Jonas, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549251/
https://www.ncbi.nlm.nih.gov/pubmed/36225598
http://dx.doi.org/10.3389/fbioe.2022.973326