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13. Inhibition of the cystic fibrosis transmembrane conductance regulator by ATP-sensitive K+ channel regulators. Sheppard DN; Welsh MJ Ann N Y Acad Sci; 1993 Dec; 707():275-84. PubMed ID: 9137558 [No Abstract] [Full Text] [Related]
14. Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. Anderson MP; Gregory RJ; Thompson S; Souza DW; Paul S; Mulligan RC; Smith AE; Welsh MJ Science; 1991 Jul; 253(5016):202-5. PubMed ID: 1712984 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains. Anderson MP; Welsh MJ Science; 1992 Sep; 257(5077):1701-4. PubMed ID: 1382316 [TBL] [Abstract][Full Text] [Related]
18. cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator. Rommens JM; Dho S; Bear CE; Kartner N; Kennedy D; Riordan JR; Tsui LC; Foskett JK Proc Natl Acad Sci U S A; 1991 Sep; 88(17):7500-4. PubMed ID: 1715567 [TBL] [Abstract][Full Text] [Related]
19. Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis. Hwang TC; Nagel G; Nairn AC; Gadsby DC Proc Natl Acad Sci U S A; 1994 May; 91(11):4698-702. PubMed ID: 7515176 [TBL] [Abstract][Full Text] [Related]
20. Pulmonary disease severity in men with deltaF508 cystic fibrosis and residual chloride secretion. Thomas SR; Jaffe A; Geddes DM; Hodson ME; Alton EW Lancet; 1999 Mar; 353(9157):984-5. PubMed ID: 10459916 [No Abstract] [Full Text] [Related] [Next] [New Search]