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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...

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Dettagli Bibliografici
Autori principali: Mastrangeli, A, Danel, C, Rosenfeld, M A, Stratford-Perricaudet, L, Perricaudet, M, Pavirani, A, Lecocq, J P, Crystal, R G
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1993
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC330018/
https://ncbi.nlm.nih.gov/pubmed/8423221
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