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....

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Detalles Bibliográficos
Autores principales: Bandara, Ranmal Avinash, Chen, Ziyan Rachel, Hu, Jim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
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

Internet

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

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