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Expression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer.

As an approach to gene therapy for the respiratory manifestations of cystic fibrosis (CF), in vivo plasmid-mediated direct transfer of the normal CF transmembrane conductance regulator (CFTR) gene to the airway epithelium was investigated in mice. To evaluate the feasibility of this strategy, pRSVL,...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Yoshimura, K, Rosenfeld, M A, Nakamura, H, Scherer, E M, Pavirani, A, Lecocq, J P, Crystal, R G
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 1992
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC312463/
https://ncbi.nlm.nih.gov/pubmed/1377820
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