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CRISPR-Cas9 genome editing using targeted lipid nanoparticles for cancer therapy
Harnessing CRISPR-Cas9 technology for cancer therapeutics has been hampered by low editing efficiency in tumors and potential toxicity of existing delivery systems. Here, we describe a safe and efficient lipid nanoparticle (LNP) for the delivery of Cas9 mRNA and sgRNAs that use a novel amino-ionizab...
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| Publicado no: | Sci Adv |
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| Principais autores: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Association for the Advancement of Science
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7673804/ https://ncbi.nlm.nih.gov/pubmed/33208369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/sciadv.abc9450 |
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