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European Journal of Biochemistry|October 1, 1993
Probing the role of metal ions in the mechanism of inositol monophosphatase by site-directed mutagenesisS J Pollack, M R Knowles, J R Atack, et al.
American Journal of Respiratory and Critical Care Medicine|June 25, 1998
Effects of topically delivered benzamil and amiloride on nasal potential difference in cystic fibrosisT Hofmann, M J Stutts, A Ziersch, et al.
British Journal of Pharmacology|April 1, 1994
Depression of high-threshold calcium currents by activation of human D2 (short) dopamine receptors expressed in differentiated NG108-15 cellsG R Seabrook, G McAllister, M R Knowles, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1985
Chloride uptake into cultured airway epithelial cells from cystic fibrosis patients and normal individualsM J Stutts, C U Cotton, J R Yankaskas, et al.
American Journal of Respiratory and Critical Care Medicine|July 1, 1996
Acute safety and effects on mucociliary clearance of aerosolized uridine 5'-triphosphate +/- amiloride in normal human adultsK N Olivier, W D Bennett, K W Hohneker, et al.
The Biochemical Journal|June 15, 1992
cDNA cloning of human and rat brain myo-inositol monophosphatase. Expression and characterization of the human recombinant enzymeG McAllister, P Whiting, E A Hammond, et al.
Genes and Immunity|June 20, 2008
Modulation of cystic fibrosis lung disease by variants in interleukin-8A D Hillian, D Londono, J M Dunn, et al.
The American Review of Respiratory Disease|October 1, 1993
Amiloride inhalation therapy in cystic fibrosis. Influence on ion content, hydration, and rheology of sputumR P Tomkiewicz, E M App, J G Zayas, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1988
Altered intestinal chloride transport in cystic fibrosisH M Berschneider, M R Knowles, R G Azizkhan, et al.
American Journal of Respiratory and Critical Care Medicine|June 25, 1998
Bronchial artery embolization for the treatment of hemoptysis in patients with cystic fibrosisG M Brinson, P G Noone, M A Mauro, et al.
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