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11. Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance. Strong TV; Wilkinson DJ; Mansoura MK; Devor DC; Henze K; Yang Y; Wilson JM; Cohn JA; Dawson DC; Frizzell RA Hum Mol Genet; 1993 Mar; 2(3):225-30. PubMed ID: 7684641 [TBL] [Abstract][Full Text] [Related]
12. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells. Rich DP; Anderson MP; Gregory RJ; Cheng SH; Paul S; Jefferson DM; McCann JD; Klinger KW; Smith AE; Welsh MJ Nature; 1990 Sep; 347(6291):358-63. PubMed ID: 1699126 [TBL] [Abstract][Full Text] [Related]
13. Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype. Beck S; Kühr J; Schütz VV; Seydewitz HH; Brandis M; Greger R; Kunzelmann K Pediatr Pulmonol; 1999 Apr; 27(4):251-9. PubMed ID: 10230924 [TBL] [Abstract][Full Text] [Related]
14. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells. Johnson LG; Boyles SE; Wilson J; Boucher RC J Clin Invest; 1995 Mar; 95(3):1377-82. PubMed ID: 7533790 [TBL] [Abstract][Full Text] [Related]
15. Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel. Berger HA; Anderson MP; Gregory RJ; Thompson S; Howard PW; Maurer RA; Mulligan R; Smith AE; Welsh MJ J Clin Invest; 1991 Oct; 88(4):1422-31. PubMed ID: 1717515 [TBL] [Abstract][Full Text] [Related]
16. Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice. Clarke LL; Grubb BR; Yankaskas JR; Cotton CU; McKenzie A; Boucher RC Proc Natl Acad Sci U S A; 1994 Jan; 91(2):479-83. PubMed ID: 7507247 [TBL] [Abstract][Full Text] [Related]
17. CFTR in Calu-3 human airway cells: channel properties and role in cAMP-activated Cl- conductance. Haws C; Finkbeiner WE; Widdicombe JH; Wine JJ Am J Physiol; 1994 May; 266(5 Pt 1):L502-12. PubMed ID: 7515579 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Disruption of monolayer integrity enables activation of a cystic fibrosis "bypass" channel in human airway epithelia. Xia Y; Haws CM; Wine JJ Nat Med; 1997 Jul; 3(7):802-5. PubMed ID: 9212112 [TBL] [Abstract][Full Text] [Related]
20. Functions of the cystic fibrosis transmembrane conductance regulator protein. Frizzell RA Am J Respir Crit Care Med; 1995 Mar; 151(3 Pt 2):S54-8. PubMed ID: 7533606 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]