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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...
Autores principales: | Soukupová, Marie, Zucchini, Silvia, Trempat, Pascal, Ingusci, Selene, Perrier-Biollay, Coline, Barbieri, Mario, Cattaneo, Stefano, Bettegazzi, Barbara, Falzoni, Simonetta, Berthommé, Hervé, Simonato, Michele |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044385/ https://www.ncbi.nlm.nih.gov/pubmed/33869657 http://dx.doi.org/10.1016/j.omtm.2021.03.020 |
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