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Potential of helper-dependent Adenoviral vectors in CRISPR-cas9-mediated lung gene therapy
Since CRISPR/Cas9 was harnessed to edit DNA, the field of gene therapy has witnessed great advances in gene editing. New avenues were created for the treatment of diseases such as Cystic Fibrosis (CF). CF is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene....
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305863/ https://www.ncbi.nlm.nih.gov/pubmed/34301308 http://dx.doi.org/10.1186/s13578-021-00662-w |