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CFTR-dependent Cl- secretion in Xenopus laevis lung epithelium. , Sommer D., Respir Physiol Neurobiol. August 15, 2007; 158 (1): 97-106.
Physiological modulation of CFTR activity by AMP-activated protein kinase in polarized T84 cells. , Hallows KR., Am J Physiol Cell Physiol. May 1, 2003; 284 (5): C1297-308.
Anion permeation in Ca(2+)-activated Cl(-) channels. , Qu Z., J Gen Physiol. December 1, 2000; 116 (6): 825-44.
Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes. , Mall M., Br J Pharmacol. August 1, 2000; 130 (8): 1884-92.
Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns. , Smith SS., J Gen Physiol. December 1, 1999; 114 (6): 799-818.
Structural and ionic determinants of 5-nitro-2-(3-phenylprophyl-amino)-benzoic acid block of the CFTR chloride channel. , Walsh KB., Br J Pharmacol. May 1, 1999; 127 (2): 369-76.
Cl- transport by cystic fibrosis transmembrane conductance regulator ( CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC. , Briel M., J Physiol. May 1, 1998; 508 ( Pt 3) 825-36.