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American Journal of Physiology. Cell Physiology|July 18, 2000
CFTR induces the expression of DRA along with Cl(-)/HCO(3)(-) exchange activity in tracheal epithelial cellsV J Wheat, H Shumaker, C Burnham, et al.
The American Journal of Physiology|March 1, 1989
Volume and ion transport by fetal rat alveolar and tracheal epithelia in submersion cultureE M Krochmal, S T Ballard, J R Yankaskas, et al.
European Journal of Respiratory Diseases. Supplement|January 1, 1987
Cell culture approaches to the investigation of human airway ion transportR C Boucher, J R Yankaskas, C U Cotton, et al.
Clinics in Chest Medicine|June 1, 1986
Abnormal respiratory epithelial ion transport in cystic fibrosisM R Knowles, M J Stutts, J R Yankaskas, et al.
The American Journal of Physiology|April 1, 1994
Mechanism of sodium hyperabsorption in cultured cystic fibrosis nasal epithelium: a patch-clamp studyT C Chinet, J M Fullton, J R Yankaskas, et al.
The American Journal of Physiology|October 1, 1993
Sodium-permeable channels in the apical membrane of human nasal epithelial cellsT C Chinet, J M Fullton, J R Yankaskas, et al.
Science (New York, N.Y.)|June 23, 1989
Persistence of abnormal chloride conductance regulation in transformed cystic fibrosis epitheliaA M Jetten, J R Yankaskas, M J Stutts, et al.
The American Review of Respiratory Disease|December 1, 1985
Culture of human nasal epithelial cells on collagen matrix supports. A comparison of bioelectric properties of normal and cystic fibrosis epitheliaJ R Yankaskas, C U Cotton, M R Knowles, et al.
The American Journal of Physiology|March 1, 1995
cAMP- but not Ca(2+)-regulated Cl- conductance in the oviduct is defective in mouse model of cystic fibrosisA Y Leung, P Y Wong, S E Gabriel, et al.
The Journal of Physiology|November 1, 1988
Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell culturesR C Boucher, C U Cotton, J T Gatzy, et al.
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