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Cre Recombinase Mediates the Removal of Bacterial Backbone to Efficiently Generate rSV40
Gene therapy has been shown to be a feasible approach to treat inherited disorders in vivo. Among the currently used viral vector systems, adeno-associated virus (AAV) vectors are the most advanced and have been applied in patients successfully. An important drawback of non-integrating AAV vectors i...
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| 出版年: | Mol Ther Methods Clin Dev |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society of Gene & Cell Therapy
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5948228/ https://ncbi.nlm.nih.gov/pubmed/29766030 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.omtm.2018.02.010 |
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