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Helper-dependent adenoviral vectors for liver-directed gene therapy
Helper-dependent adenoviral (HDAd) vectors devoid of all viral-coding sequences are promising non-integrating vectors for liver-directed gene therapy because they have a large cloning capacity, can efficiently transduce a wide variety of cell types from various species independent of the cell cycle...
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| Главные авторы: | , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Oxford University Press
2011
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3095052/ https://ncbi.nlm.nih.gov/pubmed/21470977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr143 |
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