Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
Gene transfer vectors based on adeno-associated virus (AAV) are emerging as highly promising for use in human gene therapy by virtue of their characteristics of wide host range, high transduction efficiencies, and lack of cytopathogenicity. To better define the biology of AAV-mediated gene transfer,...
Guardat en:
| Publicat a: | J Virol |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Microbiology (ASM)
1994
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC236967/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8057446/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.68.9.5656-5666.1994 |
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