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Bookmark or Share- Adeno-Associated Virus (AAV) as a Vector for Gene TherapyAdeno-associated virus (AAV) is a non-enveloped virus that can be engineered to deliver DNA to target cells, and has attracted a significant amount of attention in the field, especially in clinical-stage experimental therapeutic strategies.
- Adeno-associated virus vector as a platform for gene therapy deliveryAdeno-associated virus (AAV) vectors are the leading platform for gene delivery for the treatment of a variety of human diseases. Recent advances in developing clinically desirable AAV capsids, optimizing genome designs and harnessing revolutionary biotechnologies have contributed substantially to the growth of the gene therapy field.
- The clinical landscape for AAV gene therapies - NatureYury S. Kukushkin, Johannes C.M. van der Loo & Elaine C. Johnstone. Gene therapy using adeno-associated virus (AAV) as a vector has emerged as a novel therapeutic modality that has the...
- Adeno-associated virus as a delivery vector for gene therapy ... - NatureAdeno-associated virus (AAV) has emerged as a pivotal delivery tool in clinical gene therapy owing to its minimal pathogenicity and ability to establish long-term gene expression in...
- Adeno-associated virus vector as a platform for gene therapy ... - NatureAdeno-associated virus (AAV) vectors are the leading platform for gene delivery for the treatment of a variety of human diseases. Recent advances in developing clinically desirable AAV...
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