Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders
Bioengineering of viral vectors for therapeutic gene delivery is a pivotal strategy to reduce doses, facilitate manufacturing, and improve efficacy and patient safety. Here, we engineered myotropic adeno-associated viral (AAV) vectors via a semirational, combinatorial approach that merges AAV capsid...
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Format: | Article |
Published: |
2023
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Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/86470 |
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Institution: | Mahidol University |