The protein kinase A-regulated cardiac Cl- channel resembles the cystic fibrosis transmembrane conductance regulator.

The Mechanistic Links between Insulin and Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl- Channel.

Targeting the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Protein for the Treatment of Cystic Fibrosis.

Biosynthesis of cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis transmembrane conductance regulator and pseudomonas.

The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability.

Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore.

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.

Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.

Stoichiometry and novel gating mechanism within the cystic fibrosis transmembrane conductance regulator channel.

Regulation of the cystic fibrosis transmembrane conductance regulator anion channel by tyrosine phosphorylation.

The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation.

Cystic fibrosis transmembrane conductance regulator and the etiology and pathogenesis of cystic fibrosis.

Expression of cystic fibrosis transmembrane regulator Cl- channels in heart.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts.

Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking.

High-Potency Phenylquinoxalinone Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activators.

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Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.

Metal bridges illuminate transmembrane domain movements during gating of the cystic fibrosis transmembrane conductance regulator chloride channel.

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation.

Purification of the cystic fibrosis transmembrane conductance regulator protein expressed in Saccharomyces cerevisiae.

The Fifth Transmembrane Segment of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Its Anion Permeation Pathway.

HEK-293 cells expressing the cystic fibrosis transmembrane conductance regulator (CFTR): a model for studying regulation of Cl- transport.

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The Mechanistic Links between Insulin and Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl- Channel.

Targeting the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Protein for the Treatment of Cystic Fibrosis.

Biosynthesis of cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis transmembrane conductance regulator and pseudomonas.

The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability.

Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore.

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.

Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.

Stoichiometry and novel gating mechanism within the cystic fibrosis transmembrane conductance regulator channel.

Regulation of the cystic fibrosis transmembrane conductance regulator anion channel by tyrosine phosphorylation.

The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation.

Cystic fibrosis transmembrane conductance regulator and the etiology and pathogenesis of cystic fibrosis.

Expression of cystic fibrosis transmembrane regulator Cl- channels in heart.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts.

Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking.

High-Potency Phenylquinoxalinone Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activators.

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Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.

Metal bridges illuminate transmembrane domain movements during gating of the cystic fibrosis transmembrane conductance regulator chloride channel.

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