AbstractGaneshan et al. (Biochem Biophys. Acta 1173 (2007) 192–200) recent study documents the effect of N-WASP inhibition and actin cytoskeleton disruption on the constitutive internalization and recycling of the cystic fibrosis transmembrane conductance regulator (CFTR) channel. The results implicate the cytoskeleton network as a potential modulator of immobilized CFTR pool size at the plasma membrane and the recycling efficiency of endocytosed channel back to the cell surface
The cystic fibrosis transmembrane conductance regulator (CFTR) requires dynamic fluctuations between...
Dept. of Medical Science/박사The cystic fibrosis transmembrane conductance regulator (CFTR) is an apic...
The cystic fibrosis conductance regulator (CFTR) is a cAMP-regulated Cl(-) channel expressed predomi...
AbstractGaneshan et al. (Biochem Biophys. Acta 1173 (2007) 192–200) recent study documents the effec...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) undergoes rapid turnover at t...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl-selective anion chann...
Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator. Cystic...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a polytopic transmembrane protein ...
Biogenesis of cystic fibrosis transmembrane conductance regulator (CFTR) starts with its cotranslati...
The role of the cystic fibrosis transmembrane conductance regulator (CFTR) as a cAMP-dependent chlor...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...
The folding, misfolding, and degradation of membrane proteins is controlled by multiple processes wi...
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a member of the ATP binding cassette (...
publicationCystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is ...
Cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is expressed o...
The cystic fibrosis transmembrane conductance regulator (CFTR) requires dynamic fluctuations between...
Dept. of Medical Science/박사The cystic fibrosis transmembrane conductance regulator (CFTR) is an apic...
The cystic fibrosis conductance regulator (CFTR) is a cAMP-regulated Cl(-) channel expressed predomi...
AbstractGaneshan et al. (Biochem Biophys. Acta 1173 (2007) 192–200) recent study documents the effec...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) undergoes rapid turnover at t...
AbstractThe cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl-selective anion chann...
Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator. Cystic...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a polytopic transmembrane protein ...
Biogenesis of cystic fibrosis transmembrane conductance regulator (CFTR) starts with its cotranslati...
The role of the cystic fibrosis transmembrane conductance regulator (CFTR) as a cAMP-dependent chlor...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...
The folding, misfolding, and degradation of membrane proteins is controlled by multiple processes wi...
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a member of the ATP binding cassette (...
publicationCystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is ...
Cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is expressed o...
The cystic fibrosis transmembrane conductance regulator (CFTR) requires dynamic fluctuations between...
Dept. of Medical Science/박사The cystic fibrosis transmembrane conductance regulator (CFTR) is an apic...
The cystic fibrosis conductance regulator (CFTR) is a cAMP-regulated Cl(-) channel expressed predomi...