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Novel Cytotoxic Vectors Based on Adeno-Associated Virus
Vectors based on adeno-associated virus (AAV) are promising tools for gene therapy. The production of strongly toxic vectors, for example for cancer-directed gene transfer, is often unfeasible due to uncontrolled expression of toxic genes in vector-producing cells. Using an approach based on transcr...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3153187/ https://ncbi.nlm.nih.gov/pubmed/22069574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/toxins2122754 |
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