Better correctors are needed to repair cystic fibrosis transmembrane conductance regulator (CFTR) processing mutants that cause cystic fibrosis. Determining where the correctors bind to CFTR would aid in the development of new correctors. A recent study reported that the second nucleotide-binding domain (NBD2) was involved in binding of bithiazole correctors. Here, we show that bithiazole correctors could also rescue CFTR mutants that lacked NBD2. These results suggest that bithiazoles rescue CFTR mutants by two different mechanisms
Cystic fibrosis (CF) is a genetic disease caused by mutations that impair the function of the CFTR c...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cyclic AMP-activated chloride ch...
Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) cause ...
Cystic fibrosis (CF) is caused by loss-of-function mutations in the CF transmembrane conductance reg...
Cystic fibrosis (CF) is caused by loss-of-function mutations in the CF transmembrane conductance reg...
Conformationally constrained bithiazoles were previously found to have improved efficacy over noncon...
Small-molecule therapies that restore defects in cystic fibrosis transmembrane conductance regulator...
Cystic Fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulat...
The most common cause of cystic fibrosis (CF) is deletion of phenylalanine 508 (DeltaF508) in the CF...
The most common mutation causing cystic fibrosis (CF) is deletion of phenylalanine residue 508 in th...
Cystic fibrosis is caused primarily by deletion of Phe508. An exciting discovery was that CFTR’s sis...
Pharmacological intervention to treat the lethal genetic disease cystic fibrosis has become reality,...
SummaryMisfolding of ΔF508 cystic fibrosis (CF) transmembrane conductance regulator (CFTR) underlies...
The most common cystic fibrosis causing mutation is deletion of phenylalanine at position 508 (F508d...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel present in the m...
Cystic fibrosis (CF) is a genetic disease caused by mutations that impair the function of the CFTR c...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cyclic AMP-activated chloride ch...
Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) cause ...
Cystic fibrosis (CF) is caused by loss-of-function mutations in the CF transmembrane conductance reg...
Cystic fibrosis (CF) is caused by loss-of-function mutations in the CF transmembrane conductance reg...
Conformationally constrained bithiazoles were previously found to have improved efficacy over noncon...
Small-molecule therapies that restore defects in cystic fibrosis transmembrane conductance regulator...
Cystic Fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulat...
The most common cause of cystic fibrosis (CF) is deletion of phenylalanine 508 (DeltaF508) in the CF...
The most common mutation causing cystic fibrosis (CF) is deletion of phenylalanine residue 508 in th...
Cystic fibrosis is caused primarily by deletion of Phe508. An exciting discovery was that CFTR’s sis...
Pharmacological intervention to treat the lethal genetic disease cystic fibrosis has become reality,...
SummaryMisfolding of ΔF508 cystic fibrosis (CF) transmembrane conductance regulator (CFTR) underlies...
The most common cystic fibrosis causing mutation is deletion of phenylalanine at position 508 (F508d...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel present in the m...
Cystic fibrosis (CF) is a genetic disease caused by mutations that impair the function of the CFTR c...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cyclic AMP-activated chloride ch...
Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) cause ...