Cystic fibrosis. ATP and chloride conductance.

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

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

Cystic fibrosis transmembrane conductance regulator and pseudomonas.

Alternate pathways for chloride conductance activation in normal and cystic fibrosis airway epithelial cells.

Cystic fibrosis. Chloride channels revisited.

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.

The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor.

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

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

Biosynthesis of cystic fibrosis transmembrane conductance regulator.

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

Cystic fibrosis. Back to the chloride channel.

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

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

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

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

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

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

Extracellular ATP and UTP induce chloride secretion in nasal epithelia of cystic fibrosis patients and normal subjects in vivo.

Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts.

Cystic fibrosis transmembrane conductance regulator dysfunction in VIP knockout mice.

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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.

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Alternate pathways for chloride conductance activation in normal and cystic fibrosis airway epithelial cells.

Cystic fibrosis. Chloride channels revisited.

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.

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

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Cystic fibrosis. ATP and chloride conductance.

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