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Improvement of HSV-1 based amplicon vectors for a safe and long-lasting gene therapy in non-replicating cells
A key factor for developing gene therapy strategies for neurological disorders is the availability of suitable vectors. Currently, the most advanced are adeno-associated vectors that, while being safe and ensuring long-lasting transgene expression, have a very limited cargo capacity. In contrast, he...
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| Publicado no: | Mol Ther Methods Clin Dev |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Gene & Cell Therapy
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8044385/ https://ncbi.nlm.nih.gov/pubmed/33869657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.omtm.2021.03.020 |
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