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Supramolecular Nanosubstrate-Mediated Delivery for CRISPR/Cas9 Gene Disruption and Deletion
CRISPR/Cas9 is an efficient and precise gene editing technology that offers a versatile solution for establishing treatments directed at genetic diseases. Current CRISPR/Cas9 delivery into cells relies primarily on viral vectors, which suffer from limitations in packaging capacity and safety concern...
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| Vydáno v: | Small |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8282741/ https://ncbi.nlm.nih.gov/pubmed/34105245 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/smll.202100546 |
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