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

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

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia.

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

Biosynthesis of cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis transmembrane conductance regulator and pseudomonas.

Expression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin.

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

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

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

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

Cystic fibrosis and bone disease: defective osteoblast maturation with the F508del mutation in cystic fibrosis transmembrane conductance regulator.

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

Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives.

Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.

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

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility.

Cystic fibrosis transmembrane conductance regulator dysfunction in VIP knockout mice.

Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis-related lung disease.

Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis.

Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice.

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

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

Cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts.

Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking.

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

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia.

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

Biosynthesis of cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis transmembrane conductance regulator and pseudomonas.

Expression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin.

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

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

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

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

Cystic fibrosis and bone disease: defective osteoblast maturation with the F508del mutation in cystic fibrosis transmembrane conductance regulator.

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

Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives.

Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.

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

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility.

Cystic fibrosis transmembrane conductance regulator dysfunction in VIP knockout mice.

Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis-related lung disease.

Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis.

Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice.

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

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

Cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts.

Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking.

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

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