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Pancreatic and Intestinal Dysfunction in Cystic Fibrosis
Current Status of the Genetics of Cystic Fibrosis
Determinants and Consequences
8 other sections not shown
abnormal agonists airway cells airway epithelia amiloride amniotic fluid analysis anion apical membrane assay atropine basal membrane basolateral Boucher RC Buchwald Ca++ Canada M5G 1X8 cell cultures cell lines CF and normal CF cells CF gene CF locus CF patients channel activity chloride permeability chromosome clinical clones concentration conductance cotransporter cystic fibrosis respiratory defect depolarized disease DNA markers Editors Vol effect enzyme epithelial cells excised Farrall fetuses Figure Frizzell function HCO3 Hospital for Sick Hum Genet human chromosome hybridization hyperpolarization increased intestinal intracellular ion transport isolated isoproterenol Knowles linkage linked meconium ileus membrane potential Metacholine mucosal newborn screening Ontario oscillations pancreatic paracellular pathways Physiol polymorphic prenatal diagnosis probes Quinton reabsorptive reconstituted respiratory epithelia response Scambler secretion secretory coil sequences serosal Sick Children sodium transport studies sweat duct sweat gland tissue Toronto tracheal epithelium transepithelial trypsin Tsui L-C vesicles voltage Wainwright Widdicombe Williamson