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23. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis. Gill DR; Southern KW; Mofford KA; Seddon T; Huang L; Sorgi F; Thomson A; MacVinish LJ; Ratcliff R; Bilton D; Lane DJ; Littlewood JM; Webb AK; Middleton PG; Colledge WH; Cuthbert AW; Evans MJ; Higgins CF; Hyde SC Gene Ther; 1997 Mar; 4(3):199-209. PubMed ID: 9135733 [TBL] [Abstract][Full Text] [Related]
24. Development and analysis of recombinant adenoviruses for gene therapy of cystic fibrosis. Rich DP; Couture LA; Cardoza LM; Guiggio VM; Armentano D; Espino PC; Hehir K; Welsh MJ; Smith AE; Gregory RJ Hum Gene Ther; 1993 Aug; 4(4):461-76. PubMed ID: 7691187 [TBL] [Abstract][Full Text] [Related]
25. A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis. Knowles MR; Hohneker KW; Zhou Z; Olsen JC; Noah TL; Hu PC; Leigh MW; Engelhardt JF; Edwards LJ; Jones KR N Engl J Med; 1995 Sep; 333(13):823-31. PubMed ID: 7544439 [TBL] [Abstract][Full Text] [Related]
26. Host responses and persistence of vector genome following intrabronchial administration of an E1(-)E3(-) adenovirus gene transfer vector to normal individuals. Harvey BG; Hackett NR; Ely S; Crystal RG Mol Ther; 2001 Feb; 3(2):206-15. PubMed ID: 11237677 [TBL] [Abstract][Full Text] [Related]
27. "Sero-switch" adenovirus-mediated in vivo gene transfer: circumvention of anti-adenovirus humoral immune defenses against repeat adenovirus vector administration by changing the adenovirus serotype. Mastrangeli A; Harvey BG; Yao J; Wolff G; Kovesdi I; Crystal RG; Falck-Pedersen E Hum Gene Ther; 1996 Jan; 7(1):79-87. PubMed ID: 8825871 [TBL] [Abstract][Full Text] [Related]
28. 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; 97(6):1504-11. PubMed ID: 8617884 [TBL] [Abstract][Full Text] [Related]
30. Expression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer. Yoshimura K; Rosenfeld MA; Nakamura H; Scherer EM; Pavirani A; Lecocq JP; Crystal RG Nucleic Acids Res; 1992 Jun; 20(12):3233-40. PubMed ID: 1377820 [TBL] [Abstract][Full Text] [Related]
31. Adenovirus-mediated in vivo gene transfer. Brody SL; Crystal RG Ann N Y Acad Sci; 1994 May; 716():90-101; discussion 101-3. PubMed ID: 7517653 [TBL] [Abstract][Full Text] [Related]
32. [Prospects of gene therapy in mucoviscidosis using viral infection of the airway epithelium]. Bayle JY; Boucher RC Rev Mal Respir; 1994; 11(4):345-55. PubMed ID: 7526426 [TBL] [Abstract][Full Text] [Related]
33. 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; 362(6417):250-5. PubMed ID: 7681548 [TBL] [Abstract][Full Text] [Related]
34. CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium. Zhang L; Button B; Gabriel SE; Burkett S; Yan Y; Skiadopoulos MH; Dang YL; Vogel LN; McKay T; Mengos A; Boucher RC; Collins PL; Pickles RJ PLoS Biol; 2009 Jul; 7(7):e1000155. PubMed ID: 19621064 [TBL] [Abstract][Full Text] [Related]
35. A phase 1 study, in cystic fibrosis patients, of the safety, toxicity, and biological efficacy of a single administration of a replication deficient, recombinant adenovirus carrying the cDNA of the normal cystic fibrosis transmembrane conductance regulator gene in the lung. Crystal RG; Jaffe A; Brody S; Mastrangeli A; McElvaney NG; Rosenfeld M; Chu CS; Danel C; Hay J; Eissa T Hum Gene Ther; 1995 May; 6(5):643-66. PubMed ID: 7578401 [No Abstract] [Full Text] [Related]
36. 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; 5(6):717-29. PubMed ID: 7948134 [TBL] [Abstract][Full Text] [Related]
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38. Lentivirus-mediated gene transfer to the respiratory epithelium: a promising approach to gene therapy of cystic fibrosis. Copreni E; Penzo M; Carrabino S; Conese M Gene Ther; 2004 Oct; 11 Suppl 1():S67-75. PubMed ID: 15454960 [TBL] [Abstract][Full Text] [Related]
39. Correction of the apical membrane chloride permeability defect in polarized cystic fibrosis airway epithelia following retroviral-mediated gene transfer. Olsen JC; Johnson LG; Stutts MJ; Sarkadi B; Yankaskas JR; Swanstrom R; Boucher RC Hum Gene Ther; 1992 Jun; 3(3):253-66. PubMed ID: 1379473 [TBL] [Abstract][Full Text] [Related]
40. A phase I study of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator gene to a lung segment of individuals with cystic fibrosis. Zuckerman JB; Robinson CB; McCoy KS; Shell R; Sferra TJ; Chirmule N; Magosin SA; Propert KJ; Brown-Parr EC; Hughes JV; Tazelaar J; Baker C; Goldman MJ; Wilson JM Hum Gene Ther; 1999 Dec; 10(18):2973-85. PubMed ID: 10609658 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]