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AAV-mediated delivery of CRISPR/Cas systems for genome engineering in mammalian cells
The CRISPR/Cas9 system has emerged as a highly versatile platform for inducing targeted genome modifications into mammalian cells and model organisms. However, fully capitalizing on the therapeutic potential for this system requires its safe and efficient delivery into relevant cell types. Adeno-ass...
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| Publicado en: | Cold Spring Harb Protoc |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6850213/ https://ncbi.nlm.nih.gov/pubmed/27803249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/pdb.prot086868 |
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