selected publications
-
article
-
CFTR with a Partially Deleted R Domain Corrects the Cystic Fibrosis Chloride Transport Defect in Human Airway Epithelia in Vitro and in Mouse Nasal Muscosa in Vivo.
Proceedings of the National Academy of Sciences of the United States of America.
99:3093-3099.
-
Curcumin Stimulates Cystic Fibrosis Transmembrane Conductance Regulator CI-Channel Activity.
The Journal of Biological Chemistry.
280:5221-5227.
-
Gene Transfer of CFTR to Airway Epithelia: Low Levels of Expression are Sufficient to Correct Cl-Transpost and Overexpression can Generate Basolateral CFTR.
American Journal of Physiology. Lung Cellualr and Molecular Physiology.
33.
-
The Osmolyte Xylitol Reduces the Salt Concentration of Airway Surface Liquid and May Enhance Bacterial Killing.
Proceedings of the National Academy of Sciences of the United States of America.
97:11614-11620.
-
CFTR with a Partially Deleted R Domain Corrects the Cystic Fibrosis Chloride Transport Defect in Human Airway Epithelia in Vitro and in Mouse Nasal Muscosa in Vivo.
Proceedings of the National Academy of Sciences of the United States of America.
99:3093-3099.