Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection
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DOI: 10.3390/ijms24021246
Abstract: Cystic Fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR), a chloride/bicarbonate channel. Many studies utilize human airway cell models (cell lines and primary cells) to study different aspects of CFTR… read more here.
Keywords: cell; media selection; airway cell; cell lines ... See more keywords