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Cystic fibrosis transmembrane conductance regulator is involved in airway epithelial wound repair

The role of cystic fibrosis (CF) transmembrane conductance regulator (CFTR) in airway epithelial wound repair was investigated using normal human bronchial epithelial (NHBE) cells and a human airway epithelial cell line (Calu-3) of serous gland origin. Measurements of wound repair were performed usi...

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Hlavní autoři: Schiller, Katherine R., Maniak, Peter J., O'Grady, Scott M.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Physiological Society 2010
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2980302/
https://ncbi.nlm.nih.gov/pubmed/20686068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00215.2010
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