Cystic fibrosis. Back to the chloride channel.

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

MicroRNA-9 downregulates the ANO1 chloride channel and contributes to cystic fibrosis lung pathology.

Cystic fibrosis. Chloride channels revisited.

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

Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.

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

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

Cystic fibrosis. ATP and chloride conductance.

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

Interaction between 2 extracellular loops influences the activity of the cystic fibrosis transmembrane conductance regulator chloride channel.

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

[A flip-flop model of the chloride channel complex explains the dysregulation of the chloride flow in the plasmalemma of cells in cystic fibrosis].

Cystic fibrosis: beyond the gene to therapy.

Cystic fibrosis and non-cystic fibrosis bronchiectasis.

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

The Sweat Metabolome of Screen-Positive Cystic Fibrosis Infants: Revealing Mechanisms beyond Impaired Chloride Transport.

Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epithelia.

Activation by extracellular nucleotides of chloride secretion in the airway epithelia of patients with cystic fibrosis.

Citrate-based fluorescent materials for low-cost chloride sensing in the diagnosis of Cystic Fibrosis.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Leeds.

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

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Melbourne.

Antisense oligodeoxynucleotides to the cystic fibrosis transmembrane conductance regulator inhibit cAMP-activated but not calcium-activated chloride currents.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Copenhagen.

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

MicroRNA-9 downregulates the ANO1 chloride channel and contributes to cystic fibrosis lung pathology.

Cystic fibrosis. Chloride channels revisited.

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

Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.

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

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

Cystic fibrosis. ATP and chloride conductance.

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

Interaction between 2 extracellular loops influences the activity of the cystic fibrosis transmembrane conductance regulator chloride channel.

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

[A flip-flop model of the chloride channel complex explains the dysregulation of the chloride flow in the plasmalemma of cells in cystic fibrosis].

Cystic fibrosis: beyond the gene to therapy.

Cystic fibrosis and non-cystic fibrosis bronchiectasis.

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

The Sweat Metabolome of Screen-Positive Cystic Fibrosis Infants: Revealing Mechanisms beyond Impaired Chloride Transport.

Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epithelia.

Activation by extracellular nucleotides of chloride secretion in the airway epithelia of patients with cystic fibrosis.

Citrate-based fluorescent materials for low-cost chloride sensing in the diagnosis of Cystic Fibrosis.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Leeds.

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

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Melbourne.

Antisense oligodeoxynucleotides to the cystic fibrosis transmembrane conductance regulator inhibit cAMP-activated but not calcium-activated chloride currents.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Copenhagen.

Cystic fibrosis. Back to the chloride channel.

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