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Efficient Editing of an Adenoviral Vector Genome with CRISPR/Cas9
Immunotherapy based on genetic modification of T cells has played an important role in the treatment of tumors and viral infections. Moreover, adenoviral vectors engineered with improved safety due to their inability to integrate into the host genome have been key in the clinical application of T ce...
Gorde:
| Argitaratua izan da: | Indian J Microbiol |
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| Egile Nagusiak: | , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Springer India
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7810804/ https://ncbi.nlm.nih.gov/pubmed/33505098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12088-020-00905-3 |
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