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Characterization of basolateral K+ channels underlying anion secretion in the human airway cell line Calu-3

The Journal of physiology, 2002-02, Vol.538 (3), p.747-757

2002

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Cysteine‐independent inhibition of the CFTR chloride channel by the cysteine‐reactive reagent sodium (2‐sulphonatoethyl) methanethiosulphonate

British journal of pharmacology, 2009-07, Vol.157 (6), p.1065-1071

2009

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Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

Experimental physiology, 2006-01, Vol.91 (1), p.123-129

Linsdell, Paul

2006

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Location of a Common Inhibitor Binding Site in the Cytoplasmic Vestibule of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

The Journal of biological chemistry, 2005-03, Vol.280 (10), p.8945-8950

Linsdell, Paul

2005

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Thiocyanate as a probe of the cystic fibrosis transmembrane conductance regulator chloride channel pore

Canadian journal of physiology and pharmacology, 2001-07, Vol.79 (7), p.573-579

Linsdell, P

2001

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Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue

The Journal of physiology, 1996-11, Vol.496 (Pt 3), p.687-693

1996

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Asymmetric Structure of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore Suggested by Mutagenesis of the Twelfth Transmembrane Region

Biochemistry (Easton), 2001-06, Vol.40 (22), p.6620-6627

2001

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Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore

The Journal of physiology, 2001-02, Vol.531 (1), p.51-66

Linsdell, Paul

2001

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Flickery block of single CFTR chloride channels by intracellular anions and osmolytes

American Journal of Physiology: Cell Physiology, 1996-08, Vol.271 (2), p.C628-C634

1996

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Indazole inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels in rat epididymal epithelial cells

Biology of reproduction, 2002-12, Vol.67 (6), p.1888-1896

2002

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Na+ channel mis-expression accelerates K+ channel development in embryonic Xenopus laevis skeletal muscle

The Journal of physiology, 1994-11, Vol.480 (Pt 3), p.405-410

1994

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Cytoplasmic Loop Three of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Regulation of Chloride Channel Activity

The Journal of biological chemistry, 1996-11, Vol.271 (44), p.27493-27499

1996

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Glutathione permeability of CFTR

American Journal of Physiology: Cell Physiology, 1998-07, Vol.275 (1), p.C323-C326

1998

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Direct block of the cystic fibrosis transmembrane conductance regulator Cl − channel by butyrate and phenylbutyrate

European journal of pharmacology, 2001-01, Vol.411 (3), p.255-260

Linsdell, Paul

2001

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Direct Comparison of the Functional Roles Played by Different Transmembrane Regions in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

The Journal of biological chemistry, 2004-12, Vol.279 (53), p.55283-55289

2004

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Multiple inhibitory effects of Au(CN)(2-) ions on cystic fibrosis transmembrane conductance regulator Cl(-) channel currents

The Journal of physiology, 2002-04, Vol.540 (Pt 1), p.29-38

2002

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Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore

The Journal of general physiology, 2003-12, Vol.122 (6), p.673-687

2003

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Indazole Inhibition of Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channels in Rat Epididymal Epithelial Cells1

Biology of reproduction, 2002-12, Vol.67 (6), p.1888-1896

2002

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Inhibition of cystic fibrosis transmembrane conductance regulator chloride channel currents by arachidonic acid

Canadian journal of physiology and pharmacology, 2000-06, Vol.78 (6), p.490-499

Linsdell, P

2000

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Oxidant stress stimulates anion secretion from the human airway epithelial cell line calu-3: implications for cystic fibrosis lung disease

The Journal of physiology, 2002-08, Vol.543 (1), p.201-209

2002

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Maximization of the rate of chloride conduction in the CFTR channel pore by ion–ion interactions

Archives of biochemistry and biophysics, 2004-06, Vol.426 (1), p.78-82

2004

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Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

The Journal of general physiology, 1998-04, Vol.111 (4), p.601-614

1998

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Molecular determinants of Au(CN)(2)(-) binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl(-) channel pore

The Journal of physiology, 2002-04, Vol.540 (Pt 1), p.39

2002

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Molecular Determinants of Anion Selectivity in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

Biophysical journal, 2000-06, Vol.78 (6), p.2973-2982

2000

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Novel Regulation of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Channel Gating by External Chloride

The Journal of biological chemistry, 2004-10, Vol.279 (40), p.41658-41663

2004

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Characterization of basolateral K+ channels underlying anion secretion in the human airway cell line Calu-3

Cysteine‐independent inhibition of the CFTR chloride channel by the cysteine‐reactive reagent sodium (2‐sulphonatoethyl) methanethiosulphonate

Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

Location of a Common Inhibitor Binding Site in the Cytoplasmic Vestibule of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

Thiocyanate as a probe of the cystic fibrosis transmembrane conductance regulator chloride channel pore

Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue

Asymmetric Structure of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore Suggested by Mutagenesis of the Twelfth Transmembrane Region

Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore

Flickery block of single CFTR chloride channels by intracellular anions and osmolytes

Indazole inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels in rat epididymal epithelial cells

Na+ channel mis-expression accelerates K+ channel development in embryonic Xenopus laevis skeletal muscle

Cytoplasmic Loop Three of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Regulation of Chloride Channel Activity

Glutathione permeability of CFTR

Direct block of the cystic fibrosis transmembrane conductance regulator Cl − channel by butyrate and phenylbutyrate

Direct Comparison of the Functional Roles Played by Different Transmembrane Regions in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

Multiple inhibitory effects of Au(CN)(2-) ions on cystic fibrosis transmembrane conductance regulator Cl(-) channel currents

Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore

Indazole Inhibition of Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channels in Rat Epididymal Epithelial Cells1

Inhibition of cystic fibrosis transmembrane conductance regulator chloride channel currents by arachidonic acid

Oxidant stress stimulates anion secretion from the human airway epithelial cell line calu-3: implications for cystic fibrosis lung disease

Maximization of the rate of chloride conduction in the CFTR channel pore by ion–ion interactions

Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

Molecular determinants of Au(CN)(2)(-) binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl(-) channel pore

Molecular Determinants of Anion Selectivity in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

Novel Regulation of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Channel Gating by External Chloride

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