Definitions for "Cystic fibrosis transmembrane conductance regulator"
A protein that makes the channel in the cell where chloride moves in and out.
A prominent chloride (salt) channel present at the surface of respiratory epithelia and is dysfunctional in cystic fibrosis.
the protein that is associated with causing Cystic Fibrosis when it is mutated. Normally, it creates sweat, digestive juices, and mucus in the lungs, pancreas, and liver. When the CFTR protein has a mutation, it misfolds and becomes unable to perform its regular function.