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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 no: | Cold Spring Harb Protoc |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | 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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