Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector.
Muscle-directed gene transfer is being considered for the treatment of several metabolic diseases, including hemophilia and Duchene's muscular dystrophy. Previous efforts to target this tissue for somatic delivery with various vector systems have resulted in transient expression due to silencing of...
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| Pubblicato in: | J Virol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Microbiology (ASM)
1996
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC190884/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8892935/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.70.11.8098-8108.1996 |
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