Towards a gene therapy for cystic fibrosis lung disease.
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CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epitheliumRespiratory syncytial virus engineered to express the cystic fibrosis transmembrane conductance regulator corrects the bioelectric phenotype of human cystic fibrosis airway epithelium in vitro.
P2860
Towards a gene therapy for cystic fibrosis lung disease.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
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1997年学术文章
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1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
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1997年學術文章
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name
Towards a gene therapy for cystic fibrosis lung disease.
@en
Towards a gene therapy for cystic fibrosis lung disease.
@nl
type
label
Towards a gene therapy for cystic fibrosis lung disease.
@en
Towards a gene therapy for cystic fibrosis lung disease.
@nl
prefLabel
Towards a gene therapy for cystic fibrosis lung disease.
@en
Towards a gene therapy for cystic fibrosis lung disease.
@nl
P2860
P1476
Towards a gene therapy for cystic fibrosis lung disease.
@en
P2093
Pickles RJ
P2860
P304
P356
10.1517/13543784.6.10.1459
P407
P577
1997-10-01T00:00:00Z