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A multi-functional AAV-CRISPR-Cas9 and its host response
CRISPR-Cas9 delivery by AAV holds promise for gene therapy but faces critical barriers due to its potential immunogenicity and limited payload capacity. Here, we demonstrate genome engineering in postnatal mice using AAV-split-Cas9, a multi-functional platform customizable for genome-editing, transc...
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| Publicado no: | Nat Methods |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5374744/ https://ncbi.nlm.nih.gov/pubmed/27595405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nmeth.3993 |
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