selected publications
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article
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Contribution of Proline Residues in the Membrand-Spanning Domains of Systic Fibrosis Transmembrane Conductance Regulator to Cloride Channel Function.
The Journal of Biological Chemistry.
271:14995-15002.
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Effect of ATP Concentration on CFTR Cl{sup}-Channels: A Kinetic Analysis of Channel Regulation.
Biophysical Journal.
66.
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Effect of ATP-Sensitive K(Plus) Channel Regulators on Cystic Fibrosis Transmembrane Conductance Regulator Chloride Currents.
Journal of General Physiology.
100:573-591.
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Expression of Cystic Fibrosis Transmembrane Conductance Reulator in a Model Epithelium.
American Journal of Physiology: Lung Cellular & Molecular Physiology.
10:L405-L413.
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Function of Xenopus Cystic Fibrosis Transmembrane Conductance Regulator (CF R) Cl-Channels and Use of Human-Xenopus Chimeras to Investigate the Pore.
The Journal of Biological Chemistry.
271:25187-25192.
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Inhibition of the Cystic Fibrosis Transmembrane Conductance Regulator by ATP-Sensitive K{sup}+ Channel Regulators.
Annals of the New York Academy of Sciences.
707.
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Structure and Function of the CFTR Chloride Channel.
Physiological Reviews.
79:S23-S47.
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Contribution of Proline Residues in the Membrand-Spanning Domains of Systic Fibrosis Transmembrane Conductance Regulator to Cloride Channel Function.
The Journal of Biological Chemistry.
271:14995-15002.