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Experimental Validation of Performance Limits and Design Guidelines for Small Antennas

IEEE transactions on antennas and propagation, 2012-01, Vol.60 (1), p.8-19

2012

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Searching for laws of economics: causality, conservation, and ideology

American Journal of Physiology: Cell Physiology, 2021-03, Vol.320 (3), p.C428-C447

Dawson, David C

2021

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Cystic Fibrosis Transmembrane Conductance Regulator: A Molecular Model Defines the Architecture of the Anion Conduction Path and Locates a “Bottleneck” in the Pore

Biochemistry (Easton), 2012-03, Vol.51 (11), p.2199-2212

2012

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Cystic Fibrosis Transmembrane Conductance Regulator: Using Differential Reactivity toward Channel-Permeant and Channel-Impermeant Thiol-Reactive Probes To Test a Molecular Model for the Pore

Biochemistry (Easton), 2009-10, Vol.48 (42), p.10078-10088

2009

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Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Potentiators Protect G551D but Not ΔF508 CFTR from Thermal Instability

Biochemistry (Easton), 2014-09, Vol.53 (35), p.5613-5618

2014

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Variable Reactivity of an Engineered Cysteine at Position 338 in Cystic Fibrosis Transmembrane Conductance Regulator Reflects Different Chemical States of the Thiol

The Journal of biological chemistry, 2006-03, Vol.281 (12), p.8275-8285

2006

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CFTR: Mechanism of Anion Conduction

Physiological reviews, 1999-01, Vol.79 (1), p.47-S75

1999

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Thermal Instability of ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Channel Function: Protection by Single Suppressor Mutations and Inhibiting Channel Activity

Biochemistry (Easton), 2012-06, Vol.51 (25), p.5113-5124

2012

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Locating a plausible binding site for an open-channel blocker, GlyH-101, in the pore of the cystic fibrosis transmembrane conductance regulator

Molecular pharmacology, 2012-12, Vol.82 (6), p.1042-1055

2012

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Cystic Fibrosis Transmembrane Conductance Regulator: Temperature-Dependent Cysteine Reactivity Suggests Different Stable Conformers of the Conduction Pathway

Biochemistry (Easton), 2011-11, Vol.50 (47), p.10311-10317

2011

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WNK1 and WNK4 modulate CFTR activity

Biochemical and biophysical research communications, 2007-02, Vol.353 (3), p.535-540

2007

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CFTR: Ligand Exchange between a Permeant Anion ([Au(CN)2]−) and an Engineered Cysteine (T338C) Blocks the Pore

Biophysical journal, 2006-09, Vol.91 (5), p.1737-1748

2006

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Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns

The Journal of general physiology, 1999-12, Vol.114 (6), p.799-818

1999

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CFTR: A Cysteine at Position 338 in TM6 Senses a Positive Electrostatic Potential in the Pore

Biophysical journal, 2004-12, Vol.87 (6), p.3826-3841

2004

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Determination of the functional unit of the cystic fibrosis transmembrane conductance regulator chloride channel. One polypeptide forms one pore

The Journal of biological chemistry, 2005-01, Vol.280 (1), p.458

2005

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Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs in Xenopus Oocytes

Science (American Association for the Advancement of Science), 1991-12, Vol.254 (5039), p.1797-1799

1991

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Mercury and zinc differentially inhibit shark and human CFTR orthologues: involvement of shark cysteine 102

American Journal of Physiology: Cell Physiology, 2006-03, Vol.290 (3), p.C793-C801

2006

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CFTR: Temperature-dependent cysteine reactivity suggests different stable conformers of the conduction pathway

Biochemistry (Easton), 2011-11, Vol.50 (47), p.10311-10317

2011

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Invited Speaker CFTR: Molecular Models of the Anion Conduction Path

Biophysical journal, 2011-02, Vol.100 (3), p.363a-364a

2011

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CFTR: covalent modification of cysteine-substituted channels expressed in Xenopus oocytes shows that activation is due to the opening of channels resident in the plasma membrane

The Journal of general physiology, 2001-10, Vol.118 (4), p.433

2001

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Determination of the Functional Unit of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel

The Journal of biological chemistry, 2005-01, Vol.280 (1), p.458-468

2005

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Functional Roles of the Nucleotide-Binding Folds in the Activation of the Cystic Fibrosis Transmembrane Conductance Regulator

Proceedings of the National Academy of Sciences - PNAS, 1993-11, Vol.90 (21), p.9963-9967

1993

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Voltage-sensitive gating induced by a mutation in the fifth transmembrane domain of CFTR

American journal of physiology. Lung cellular and molecular physiology, 2002-01, Vol.282 (1), p.135-L145

2002

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Structural Basis for the State-Dependent Reactivity of Engineered Cysteines in the Pore of the CFTR Channel

Biophysical journal, 2013-01, Vol.104 (2), p.625a-625a

2013

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THERMAL INSTABILITY OF ΔF508 CFTR CHANNEL FUNCTION: PROTECTION BY SINGLE SUPPRESSOR MUTATIONS AND INHIBITING CHANNEL ACTIVITY

Biochemistry (Easton), 2012-06, Vol.51 (25), p.5113-5124

2012

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Experimental Validation of Performance Limits and Design Guidelines for Small Antennas

Searching for laws of economics: causality, conservation, and ideology

Cystic Fibrosis Transmembrane Conductance Regulator: A Molecular Model Defines the Architecture of the Anion Conduction Path and Locates a “Bottleneck” in the Pore

Cystic Fibrosis Transmembrane Conductance Regulator: Using Differential Reactivity toward Channel-Permeant and Channel-Impermeant Thiol-Reactive Probes To Test a Molecular Model for the Pore

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Potentiators Protect G551D but Not ΔF508 CFTR from Thermal Instability

Variable Reactivity of an Engineered Cysteine at Position 338 in Cystic Fibrosis Transmembrane Conductance Regulator Reflects Different Chemical States of the Thiol

CFTR: Mechanism of Anion Conduction

Thermal Instability of ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Channel Function: Protection by Single Suppressor Mutations and Inhibiting Channel Activity

Locating a plausible binding site for an open-channel blocker, GlyH-101, in the pore of the cystic fibrosis transmembrane conductance regulator

Cystic Fibrosis Transmembrane Conductance Regulator: Temperature-Dependent Cysteine Reactivity Suggests Different Stable Conformers of the Conduction Pathway

WNK1 and WNK4 modulate CFTR activity

CFTR: Ligand Exchange between a Permeant Anion ([Au(CN)2]−) and an Engineered Cysteine (T338C) Blocks the Pore

Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns

CFTR: A Cysteine at Position 338 in TM6 Senses a Positive Electrostatic Potential in the Pore

Determination of the functional unit of the cystic fibrosis transmembrane conductance regulator chloride channel. One polypeptide forms one pore

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs in Xenopus Oocytes

Mercury and zinc differentially inhibit shark and human CFTR orthologues: involvement of shark cysteine 102

CFTR: Temperature-dependent cysteine reactivity suggests different stable conformers of the conduction pathway

Invited Speaker CFTR: Molecular Models of the Anion Conduction Path

CFTR: covalent modification of cysteine-substituted channels expressed in Xenopus oocytes shows that activation is due to the opening of channels resident in the plasma membrane

Determination of the Functional Unit of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel

Functional Roles of the Nucleotide-Binding Folds in the Activation of the Cystic Fibrosis Transmembrane Conductance Regulator

Voltage-sensitive gating induced by a mutation in the fifth transmembrane domain of CFTR

Structural Basis for the State-Dependent Reactivity of Engineered Cysteines in the Pore of the CFTR Channel

THERMAL INSTABILITY OF ΔF508 CFTR CHANNEL FUNCTION: PROTECTION BY SINGLE SUPPRESSOR MUTATIONS AND INHIBITING CHANNEL ACTIVITY

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