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Delivery Approaches for CRISPR/Cas9 Therapeutics In Vivo: Advances and Challenges
Therapeutic gene editing is becoming a viable biomedical tool with the emergence of the CRISPR/Cas9 system. CRISPR-based technologies have promise as a therapeutic platform for many human genetic diseases previously considered untreatable, providing a flexible approach to high-fidelity gene editing....
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| Publicado no: | Expert Opin Drug Deliv |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6295289/ https://ncbi.nlm.nih.gov/pubmed/30169977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/17425247.2018.1517746 |
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