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...
محفوظ في:
| الحاوية / القاعدة: | J Virol |
|---|---|
| المؤلفون الرئيسيون: | , , |
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
American Society for Microbiology (ASM)
1996
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| الموضوعات: | |
| الوصول للمادة أونلاين: | 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 |
| الوسوم: |
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