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Population-wide gene disruption in the murine lung epithelium via AAV-mediated delivery of CRISPR-Cas9 components
With the aim of expediting drug target discovery and validation for respiratory diseases, we developed an optimized method for in situ somatic gene disruption in murine lung epithelial cells via AAV6-mediated CRISPR-Cas9 delivery. Efficient gene editing was observed in lung type II alveolar epitheli...
Autores principales: | Chen, Honglin, Durinck, Steffen, Patel, Hetal, Foreman, Oded, Mesh, Kathryn, Eastham, Jeffrey, Caothien, Roger, Newman, Robert J., Roose-Girma, Merone, Darmanis, Spyros, Warming, Soren, Lattanzi, Annalisa, Liang, Yuxin, Haley, Benjamin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668740/ https://www.ncbi.nlm.nih.gov/pubmed/36419469 http://dx.doi.org/10.1016/j.omtm.2022.10.016 |
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