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180 related items for PubMed ID: 8789091
1. Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel. Tao T, Xie J, Drumm ML, Zhao J, Davis PB, Ma J. Biophys J; 1996 Feb; 70(2):743-53. PubMed ID: 8789091 [Abstract] [Full Text] [Related]
2. Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations. Zhao J, Zerhusen B, Xie J, Drumm ML, Davis PB, Ma J. Biophys J; 1996 Nov; 71(5):2458-66. PubMed ID: 8913585 [Abstract] [Full Text] [Related]
3. Human epithelial cystic fibrosis transmembrane conductance regulator without exon 5 maintains partial chloride channel function in intracellular membranes. Xie J, Drumm ML, Zhao J, Ma J, Davis PB. Biophys J; 1996 Dec; 71(6):3148-56. PubMed ID: 8968585 [Abstract] [Full Text] [Related]
11. Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis. Gunderson KL, Kopito RR. Cell; 1995 Jul 28; 82(2):231-9. PubMed ID: 7543023 [Abstract] [Full Text] [Related]
12. The two halves of CFTR form a dual-pore ion channel. Yue H, Devidas S, Guggino WB. J Biol Chem; 2000 Apr 07; 275(14):10030-4. PubMed ID: 10744680 [Abstract] [Full Text] [Related]
13. Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents. Cai Z, Lansdell KA, Sheppard DN. Br J Pharmacol; 1999 Sep 07; 128(1):108-18. PubMed ID: 10498841 [Abstract] [Full Text] [Related]
14. Functional and pharmacological induced structural changes of the cystic fibrosis transmembrane conductance regulator in the membrane solved using SAXS. Baroni D, Zegarra-Moran O, Moran O. Cell Mol Life Sci; 2015 Apr 07; 72(7):1363-75. PubMed ID: 25274064 [Abstract] [Full Text] [Related]
17. Function of the R domain in the cystic fibrosis transmembrane conductance regulator chloride channel. Ma J, Zhao J, Drumm ML, Xie J, Davis PB. J Biol Chem; 1997 Oct 31; 272(44):28133-41. PubMed ID: 9346969 [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 01; 102(11):1986-93. PubMed ID: 9835624 [Abstract] [Full Text] [Related]