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6. [Cellular expression of CFTR in cystic fibrosis: defective cyclic AMP-dependent regulation of glycoconjugate secretion in cystic fibrosis fetal tracheal epithelial cells transfected by SV40 large T oncogene]. Picard J, Lemnaouar M, Paul A. Bull Acad Natl Med; 1993 Mar 27; 177(3):383-93; discussion 393-4. PubMed ID: 7689916 [Abstract] [Full Text] [Related]
15. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients. Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C. Hepatology; 1999 Jun 01; 29(6):1624-34. PubMed ID: 10347100 [Abstract] [Full Text] [Related]
17. GTP-binding proteins inhibit cAMP activation of chloride channels in cystic fibrosis airway epithelial cells. Schwiebert EM, Kizer N, Gruenert DC, Stanton BA. Proc Natl Acad Sci U S A; 1992 Nov 15; 89(22):10623-7. PubMed ID: 1279687 [Abstract] [Full Text] [Related]
18. Ketoconazole activates Cl- conductance and blocks Cl- and fluid absorption by cultured cystic fibrosis (CFPAC-1) cells. Kersting U, Kersting D, Spring KR. Proc Natl Acad Sci U S A; 1993 May 01; 90(9):4047-51. PubMed ID: 7683418 [Abstract] [Full Text] [Related]