(Cystic Fibrosis Transmembrane conductance Regulator)
Cystic fibrosis transmembrane conductance regulator (CFTR) functions as a chloride channel and controls the regulation of other transport pathways. Mutations in the CFTR gene have been found to cause cystic fibrosis (CF) and congenital bilateral aplasia of the vas deferens (CBAVD).
- View An Official American Thoracic Society Workshop Report: Translational Research in Rare Respiratory Diseases Year: 2017
- View Development of Automated Patch Clamp Technique to Investigate CFTR Chloride Channel Function Year: 2017
- View QPatch: the missing link between HTS and ion channel drug discovery. Year: 2009
- View Mashiningan improves opioid-induced constipation in rats by activating cystic fibrosis transmembrane conductance regulator chloride channel Year: 2017