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23. 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; Greger R; Kunzelmann K J Physiol; 1998 May; 508 ( Pt 3)(Pt 3):825-36. PubMed ID: 9518736 [TBL] [Abstract][Full Text] [Related]
24. CFTR null mutation altered cAMP-sensitive and swelling-activated Cl- currents in primary cultures of mouse nephron. Barrière H; Belfodil R; Rubera I; Tauc M; Poujeol C; Bidet M; Poujeol P Am J Physiol Renal Physiol; 2003 Apr; 284(4):F796-811. PubMed ID: 12475744 [TBL] [Abstract][Full Text] [Related]
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26. Inhibition of ENaC by intracellular Cl- in an MDCK clone with high ENaC expression. Xie Y; Schafer JA Am J Physiol Renal Physiol; 2004 Oct; 287(4):F722-31. PubMed ID: 15161604 [TBL] [Abstract][Full Text] [Related]
27. Basolateral adrenoceptor activation mediates noradrenaline-induced Cl- secretion in M-1 mouse cortical collecting duct cells. Cuffe JE; Howard DP; Bertog M; Korbmacher C Pflugers Arch; 2002 Dec; 445(3):381-9. PubMed ID: 12466941 [TBL] [Abstract][Full Text] [Related]
34. Liddle's syndrome mutations increase Na+ transport through dual effects on epithelial Na+ channel surface expression and proteolytic cleavage. Knight KK; Olson DR; Zhou R; Snyder PM Proc Natl Acad Sci U S A; 2006 Feb; 103(8):2805-8. PubMed ID: 16477034 [TBL] [Abstract][Full Text] [Related]
35. Cl- absorption across the thick ascending limb is not altered in cystic fibrosis mice. A role for a pseudo-CFTR Cl- channel. Marvão P; De Jesus Ferreira MC; Bailly C; Paulais M; Bens M; Guinamard R; Moreau R; Vandewalle A; Teulon J J Clin Invest; 1998 Dec; 102(11):1986-93. PubMed ID: 9835624 [TBL] [Abstract][Full Text] [Related]