Optimization of AAV vectors to target persistent viral reservoirs

Gene delivery of antiviral therapeutics to anatomical sites where viruses accumulate and persist is a promising approach for the next generation of antiviral therapies. Recombinant adeno-associated viruses (AAV) are one of the leading vectors for gene therapy applications that deliver gene-editing e...

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Detalles Bibliográficos
Autores principales: Colón-Thillet, Rossana, Jerome, Keith R., Stone, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067653/
https://www.ncbi.nlm.nih.gov/pubmed/33892762
http://dx.doi.org/10.1186/s12985-021-01555-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067653/
https://www.ncbi.nlm.nih.gov/pubmed/33892762
http://dx.doi.org/10.1186/s12985-021-01555-7

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