Retroviral vector particles displaying the antigen-binding site of an antibody enable cell-type-specific gene transfer.
Retroviral vectors are the most efficient tool for stably introducing genes into vertebrate cells. However, their use is limited by the host range of the retrovirus from which they are derived. To alter the host range, we recently constructed retrovirus vector particles, derived from spleen necrosis...
Uloženo v:
| Vydáno v: | J Virol |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Microbiology (ASM)
1995
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC188950/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7884919/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.69.4.2659-2663.1995 |
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