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cystic fibrosis transmembrane conductance regulator

BACKGROUND Increasing the activity of defective cystic fibrosis transmembrane conductance regulator (CFTR) protein is a potential treatment for cystic fibrosis.

The expression of cystic fibrosis transmembrane conductance regulator and aquaporin-1 in the human hydrosalpinx

The protective effects of cystic fibrosis transmembrane conductance regulator chloride channel on injured human alveolar epithelial cells

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