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26. Cellular differentiation is required for cAMP but not Ca(2+)-dependent Cl- secretion in colonic epithelial cells expressing high levels of cystic fibrosis transmembrane conductance regulator. Morris AP, Cunningham SA, Benos DJ, Frizzell RA. J Biol Chem; 1992 Mar 15; 267(8):5575-83. PubMed ID: 1372005 [Abstract] [Full Text] [Related]
27. The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel. Reisin IL, Prat AG, Abraham EH, Amara JF, Gregory RJ, Ausiello DA, Cantiello HF. J Biol Chem; 1994 Aug 12; 269(32):20584-91. PubMed ID: 7519611 [Abstract] [Full Text] [Related]
30. The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells. Lukacs GL, Chang XB, Bear C, Kartner N, Mohamed A, Riordan JR, Grinstein S. J Biol Chem; 1993 Oct 15; 268(29):21592-8. PubMed ID: 7691813 [Abstract] [Full Text] [Related]
32. A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules. Zerhusen B, Zhao J, Xie J, Davis PB, Ma J. J Biol Chem; 1999 Mar 19; 274(12):7627-30. PubMed ID: 10075649 [Abstract] [Full Text] [Related]
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37. 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 28; 2(3):225-30. PubMed ID: 7684641 [Abstract] [Full Text] [Related]