selected publications
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article
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Contribution of R Domain Phosphoserines to the Function of CFTR Studied in Fischer Rat Thyroid Epithelia.
American Journal of Physiology.
23:L835-L841.
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Fluoride Stimulates Cystic Fibrosis Transmembrane Conductance Regulator CI-Channel Activity.
American Journal of Physiology: Lung Cellular & Molecular Physiology.
18:L305-L312.
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Physiology in Medicine Electrolyte Transport in the Lungs. The Crucial Physiologic Role of Such Transport is Underscored by itsLethal Derangement in Cystic Fibrosis. Normal and Deranged Mechanisms are Described.
Hospital Practice.
26.
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Protein Phosphatase 2C Dephosphorylates And Inactivates Cystic Fibrosis Transmembrane Conductance Regulator.
Proceedings of the National Academy of Sciences of the United States of America.
94:11055-11060.
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Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Cl{sup}- Channel by Specific Protein Kinases and Protein Phosphatases.
The Journal of Biological Chemistry.
268.
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Contribution of R Domain Phosphoserines to the Function of CFTR Studied in Fischer Rat Thyroid Epithelia.
American Journal of Physiology.
23:L835-L841.