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2. 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]
3. How ATP regulates the CFT regulator. DeFelice LJ Biophys J; 1994 May; 66(5):1268-9. PubMed ID: 7520288 [No Abstract] [Full Text] [Related]
4. Noise analysis and single-channel observations of 4 pS chloride channels in human airway epithelia. Duszyk M; French AS; Man SF Biophys J; 1992 Feb; 61(2):583-7. PubMed ID: 1372182 [TBL] [Abstract][Full Text] [Related]
5. Towards the biochemical defect in cystic fibrosis. Lancet; 1989 Dec; 2(8677):1433. PubMed ID: 2480500 [No Abstract] [Full Text] [Related]
11. Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites. Chang XB; Tabcharani JA; Hou YX; Jensen TJ; Kartner N; Alon N; Hanrahan JW; Riordan JR J Biol Chem; 1993 May; 268(15):11304-11. PubMed ID: 7684377 [TBL] [Abstract][Full Text] [Related]
12. Some properties of sodium and chloride channels in respiratory epithelia of CF- and non-CF-patients. Disser J; Hazama A; Frömter E Adv Exp Med Biol; 1991; 290():133-41; discussion 141-4. PubMed ID: 1719754 [No Abstract] [Full Text] [Related]
13. Guanabenz, an alpha2-selective adrenergic agonist, activates Ca2+-dependent chloride currents in cystic fibrosis human airway epithelial cells. Norez C; Vandebrouck C; Antigny F; Dannhoffer L; Blondel M; Becq F Eur J Pharmacol; 2008 Sep; 592(1-3):33-40. PubMed ID: 18640110 [TBL] [Abstract][Full Text] [Related]
14. Cystic fibrosis. Sickly channels in mild disease. Miller C Nature; 1993 Mar; 362(6416):106. PubMed ID: 7680767 [No Abstract] [Full Text] [Related]
15. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive. Denning GM; Anderson MP; Amara JF; Marshall J; Smith AE; Welsh MJ Nature; 1992 Aug; 358(6389):761-4. PubMed ID: 1380673 [TBL] [Abstract][Full Text] [Related]
16. Dysfunction of CFTR bearing the delta F508 mutation. Welsh MJ; Denning GM; Ostedgaard LS; Anderson MP J Cell Sci Suppl; 1993; 17():235-9. PubMed ID: 7511616 [TBL] [Abstract][Full Text] [Related]
17. Cystic fibrosis transmembrane conductance regulator protein: what is its role in cystic fibrosis? Richardson PS; Alton EW Eur Respir J; 1993 Feb; 6(2):160-2. PubMed ID: 7680321 [No Abstract] [Full Text] [Related]
18. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Welsh MJ; Smith AE Cell; 1993 Jul; 73(7):1251-4. PubMed ID: 7686820 [No Abstract] [Full Text] [Related]
19. Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulation. Winter MC; Sheppard DN; Carson MR; Welsh MJ Biophys J; 1994 May; 66(5):1398-403. PubMed ID: 7520292 [TBL] [Abstract][Full Text] [Related]
20. CFTR anion channel modulates expression of human transmembrane mucin MUC3 through the PDZ protein GOPC. Pelaseyed T; Hansson GC J Cell Sci; 2011 Sep; 124(Pt 18):3074-83. PubMed ID: 21852426 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]