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698 related items for PubMed ID: 7519885
21. 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; 5(9):1121-9. PubMed ID: 7530494 [Abstract] [Full Text] [Related]
22. Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis. Zabner J, Ramsey BW, Meeker DP, Aitken ML, Balfour RP, Gibson RL, Launspach J, Moscicki RA, Richards SM, Standaert TA. J Clin Invest; 1996 Mar 15; 97(6):1504-11. PubMed ID: 8617884 [Abstract] [Full Text] [Related]
23. Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy. Hyde SC, Gill DR, Higgins CF, Trezise AE, MacVinish LJ, Cuthbert AW, Ratcliff R, Evans MJ, Colledge WH. Nature; 1993 Mar 18; 362(6417):250-5. PubMed ID: 7681548 [Abstract] [Full Text] [Related]
24. Evaluation of the efficacy and safety of in vitro, adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator cDNA. Mittereder N, Yei S, Bachurski C, Cuppoletti J, Whitsett JA, Tolstoshev P, Trapnell BC. Hum Gene Ther; 1994 Jun 18; 5(6):717-29. PubMed ID: 7948134 [Abstract] [Full Text] [Related]
29. Gene therapy in a xenograft model of cystic fibrosis lung corrects chloride transport more effectively than the sodium defect. Goldman MJ, Yang Y, Wilson JM. Nat Genet; 1995 Feb 18; 9(2):126-31. PubMed ID: 7719338 [Abstract] [Full Text] [Related]
30. Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model. Potash AE, Wallen TJ, Karp PH, Ernst S, Moninger TO, Gansemer ND, Stoltz DA, Zabner J, Chang EH. Mol Ther; 2013 May 18; 21(5):947-53. PubMed ID: 23511247 [Abstract] [Full Text] [Related]