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Efficient transduction of myeloid cells by a lentiviral vector that packages the Vpx accessory protein
Lentiviral vectors are widely used for the stable expression of genes and shRNA-mediated knockdown and are currently under development for clinical use in gene therapy. Pseudotyping of the vectors with VSV-G allows them to infect a wide range of cell-types. However, myeloid cells, such as dendritic...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4105013/ https://ncbi.nlm.nih.gov/pubmed/22895508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gt.2012.61 |
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