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Adenoviral targeting using genetically incorporated camelid single variable domains
The unique ability of human adenovirus serotype 5 (Ad5) to accomplish efficient transduction has allowed the use of Ad5-based vectors for a range of gene therapy applications. Several strategies have been developed to alter tropism of Ad vectors to achieve a cell-specific gene delivery by employing...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4157633/ https://ncbi.nlm.nih.gov/pubmed/24933423 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/labinvest.2014.82 |
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