Add to ORKGII. Cystic Fibrosis Transmembrane Conductance Regulator-Outwardly Rectifying Chloride Channel Regulatory Interaction S146 A. Importance of cytoplasmic ATP S147 B. Importance of ATP release mechanisms and purinergic receptors S14
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride ion channel whose defec...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl-selective anion chann...
HEK-293 cells expressing the cystic fibrosis transmembrane conductance regulator (CFTR): a model for...
Abstract The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl − channel that gover...
SummaryThe cystic fibrosis transmembrane conductance regulator(CFTR) functions to regulate both CI− ...
Cystic fibrosis transmembrane conductance regulator (CFTR) is an ATP-gated anion channel with two re...
The CFTR gene is unique within the ATP-binding cassette (ABC) protein family, predominantly of trans...
The cystic fibrosis transmembrane conductance regu-lator (CFTR) is a cAMP-regulated chloride channel...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-activated Cl- channel that ...
Cystic fibrosis (CF) is a lethal autosomal recessive genetic disease caused by mutations in the CF t...
CFTR, the chloride ion channel encoded by the gene mutated in cystic fibrosis patients, has been the...
Conference Theme: A Century of Advances in Physiology, Biophysics and Neuroscienc
CFTR protein is an ion channel regulated by cAMP-dependent phosphorylation and expressed in many typ...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...
Cystic fibrosis tnsmembrane conductance regulator (CFTR) generates cAMP-regulated channels; mutation...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride ion channel whose defec...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl-selective anion chann...
HEK-293 cells expressing the cystic fibrosis transmembrane conductance regulator (CFTR): a model for...
Abstract The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl − channel that gover...
SummaryThe cystic fibrosis transmembrane conductance regulator(CFTR) functions to regulate both CI− ...
Cystic fibrosis transmembrane conductance regulator (CFTR) is an ATP-gated anion channel with two re...
The CFTR gene is unique within the ATP-binding cassette (ABC) protein family, predominantly of trans...
The cystic fibrosis transmembrane conductance regu-lator (CFTR) is a cAMP-regulated chloride channel...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-activated Cl- channel that ...
Cystic fibrosis (CF) is a lethal autosomal recessive genetic disease caused by mutations in the CF t...
CFTR, the chloride ion channel encoded by the gene mutated in cystic fibrosis patients, has been the...
Conference Theme: A Century of Advances in Physiology, Biophysics and Neuroscienc
CFTR protein is an ion channel regulated by cAMP-dependent phosphorylation and expressed in many typ...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...
Cystic fibrosis tnsmembrane conductance regulator (CFTR) generates cAMP-regulated channels; mutation...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride ion channel whose defec...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl-selective anion chann...
HEK-293 cells expressing the cystic fibrosis transmembrane conductance regulator (CFTR): a model for...