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Challenges and Prospects for Helper-Dependent Adenoviral Vector-Mediated Gene Therapy
Helper-dependent adenoviral (HDAd) vectors that are devoid of all viral coding sequences are promising non-integrating vectors for gene therapy because they efficiently transduce a variety of cell types in vivo, have a large cloning capacity, and drive long-term transgene expression without chronic...
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| Veröffentlicht in: | Biomedicines |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
MDPI
2014
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5423471/ https://ncbi.nlm.nih.gov/pubmed/28548064 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biomedicines2020132 |
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