Generation of recombinant adenovirus vectors with modified fibers for altering viral tropism.
To expand the utility of recombinant adenovirus vectors for gene therapy applications, methods to alter native viral tropism to achieve cell-specific transduction would be beneficial. To this end, we are pursuing genetic methods to alter the cell recognition domain of the adenovirus fiber. To incorp...
Uloženo v:
| Vydáno v: | J Virol |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Microbiology (ASM)
1996
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC190731/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8794325/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.70.10.6839-6846.1996 |
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