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261 related items for PubMed ID: 1698126
1. Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer. Drumm ML, Pope HA, Cliff WH, Rommens JM, Marvin SA, Tsui LC, Collins FS, Frizzell RA, Wilson JM. Cell; 1990 Sep 21; 62(6):1227-33. PubMed ID: 1698126 [Abstract] [Full Text] [Related]
5. 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 21; 2(3):225-30. PubMed ID: 7684641 [Abstract] [Full Text] [Related]
7. Human lymphocytes transcribe the cystic fibrosis transmembrane conductance regulator gene and exhibit CF-defective cAMP-regulated chloride current. McDonald TV, Nghiem PT, Gardner P, Martens CL. J Biol Chem; 1992 Feb 15; 267(5):3242-8. PubMed ID: 1371114 [Abstract] [Full Text] [Related]
8. Targeting of carbonic anhydrase IV to plasma membranes is altered in cultured human pancreatic duct cells expressing a mutated (deltaF508) CFTR. Fanjul M, Salvador C, Alvarez L, Cantet S, Hollande E. Eur J Cell Biol; 2002 Aug 15; 81(8):437-47. PubMed ID: 12234015 [Abstract] [Full Text] [Related]
11. Increasing expression of the normal human CFTR cDNA in cystic fibrosis epithelial cells results in a progressive increase in the level of CFTR protein expression, but a limit on the level of cAMP-stimulated chloride secretion. Rosenfeld MA, Rosenfeld SJ, Danel C, Banks TC, Crystal RG. Hum Gene Ther; 1994 Sep 15; 5(9):1121-9. PubMed ID: 7530494 [Abstract] [Full Text] [Related]
12. 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 01; 88(17):7500-4. PubMed ID: 1715567 [Abstract] [Full Text] [Related]