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Systemic Gene Transfer to Skeletal Muscle Using Reengineered AAV Vectors
Gene therapy of musculoskeletal disorders warrants efficient gene transfer to a wide range of muscle groups. Reengineered adeno-associated viral (AAV) vectors that selectively transduce muscle tissue following systemic administration are attractive candidates for such applications. Here we provide e...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3253371/ https://ncbi.nlm.nih.gov/pubmed/21194026 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-61737-982-6_9 |
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