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Pseudotyped lentiviral vectors: Ready for translation into targeted cancer gene therapy?
Gene therapy holds great promise for curing cancer by editing the deleterious genes of tumor cells, but the lack of vector systems for efficient delivery of genetic material into specific tumor sites in vivo has limited its full therapeutic potential in cancer gene therapy. Over the past two decades...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Chongqing Medical University
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363566/ https://www.ncbi.nlm.nih.gov/pubmed/37492721 http://dx.doi.org/10.1016/j.gendis.2022.03.007 |