Diversity of airway epithelial cell targets for in vivo recombinant adenovirus-mediated gene transfer.
A variety of pulmonary disorders, including cystic fibrosis, are potentially amenable to treatment in which a therapeutic gene is directly transferred to the bronchial epithelium. This is difficult to accomplish because the majority of airway epithelial cells replicate slowly and/or are terminally d...
Kaydedildi:
| Yayımlandı: | J Clin Invest |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society for Clinical Investigation
1993
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC330018/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8423221/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116175 |
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