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Comparison of Transduction Efficiency of Tyrosine-Mutant AAV Serotype Vectors in Kidney
1. Gene therapy has a distinct potential to treat kidney diseases. However, the efficient transduction of a significant number of renal cells by viral vectors has been difficult to accomplish. Previous studies have indicated that adeno-associated virus (AAV) can transduce renal cells with variable a...
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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3621769/ https://ncbi.nlm.nih.gov/pubmed/23216315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/1440-1681.12037 |
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