116 related articles for article (PubMed ID: 10657937)
1. Efficient gene transfer into human normal and cystic fibrosis tracheal gland serous cells with synthetic vectors.
Allo JC; Midoux P; Merten M; Souil E; Lipecka J; Figarella C; Monsigny M; Briand P; Fajac I
Am J Respir Cell Mol Biol; 2000 Feb; 22(2):166-75. PubMed ID: 10657937
[TBL] [Abstract][Full Text] [Related]
2. Sugar-mediated uptake of glycosylated polylysines and gene transfer into normal and cystic fibrosis airway epithelial cells.
Fajac I; Briand P; Monsigny M; Midoux P
Hum Gene Ther; 1999 Feb; 10(3):395-406. PubMed ID: 10048392
[TBL] [Abstract][Full Text] [Related]
3. Histidylated polylysine as a synthetic vector for gene transfer into immortalized cystic fibrosis airway surface and airway gland serous cells.
Fajac I; Allo JC; Souil E; Merten M; Pichon C; Figarella C; Monsigny M; Briand P; Midoux P
J Gene Med; 2000; 2(5):368-78. PubMed ID: 11045431
[TBL] [Abstract][Full Text] [Related]
4. A cystic fibrosis tracheal gland cell line, CF-KM4. Correction by adenovirus-mediated CFTR gene transfer.
Kammouni W; Moreau B; Becq F; Saleh A; Pavirani A; Figarella C; Merten MD
Am J Respir Cell Mol Biol; 1999 Apr; 20(4):684-91. PubMed ID: 10101000
[TBL] [Abstract][Full Text] [Related]
5. Inhibition by TNF-alpha and IL-4 of cationic lipid mediated gene transfer in cystic fibrosis tracheal gland cells.
Bastonero S; Gargouri M; Ortiou S; Guéant JL; Merten MD
J Gene Med; 2005 Nov; 7(11):1439-49. PubMed ID: 16001392
[TBL] [Abstract][Full Text] [Related]
6. Uptake of plasmid/glycosylated polymer complexes and gene transfer efficiency in differentiated airway epithelial cells.
Fajac I; Thévenot G; Bédouet L; Danel C; Riquet M; Merten M; Figarella C; Dall'Ava-Santucci J; Monsigny M; Briand P
J Gene Med; 2003 Jan; 5(1):38-48. PubMed ID: 12516050
[TBL] [Abstract][Full Text] [Related]
7. Restoration of cyclic adenosine monophosphate-stimulated chloride channel activity in human cystic fibrosis tracheobronchial submucosal gland cells by adenovirus-mediated and cationic lipid-mediated gene transfer.
Jiang C; Finkbeiner WE; Widdicombe JH; Fang SL; Wang KX; Nietupski JB; Hehir KM; Cheng SH
Am J Respir Cell Mol Biol; 1999 Jun; 20(6):1107-15. PubMed ID: 10340929
[TBL] [Abstract][Full Text] [Related]
8. Mechanism of restriction of normal and cystic fibrosis transmembrane conductance regulator-deficient human tracheal gland cells to adenovirus infection and ad-mediated gene transfer.
Gaden F; Franqueville L; Hong SS; Legrand V; Figarella C; Boulanger P
Am J Respir Cell Mol Biol; 2002 Nov; 27(5):628-40. PubMed ID: 12397023
[TBL] [Abstract][Full Text] [Related]
9. Cellular localization and activity of Ad-delivered GFP-CFTR in airway epithelial and tracheal cells.
Granio O; Norez C; Ashbourne Excoffon KJ; Karp PH; Lusky M; Becq F; Boulanger P; Zabner J; Hong SS
Am J Respir Cell Mol Biol; 2007 Dec; 37(6):631-9. PubMed ID: 17641299
[TBL] [Abstract][Full Text] [Related]
10. Gluconoylated and glycosylated polylysines as vectors for gene transfer into cystic fibrosis airway epithelial cells.
Kollen WJ; Midoux P; Erbacher P; Yip A; Roche AC; Monsigny M; Glick MC; Scanlin TF
Hum Gene Ther; 1996 Aug; 7(13):1577-86. PubMed ID: 8864758
[TBL] [Abstract][Full Text] [Related]
11. Salmeterol restores secretory functions in cystic fibrosis airway submucosal gland serous cells.
Delavoie F; Molinari M; Milliot M; Zahm JM; Coraux C; Michel J; Balossier G
Am J Respir Cell Mol Biol; 2009 Apr; 40(4):388-97. PubMed ID: 18931328
[TBL] [Abstract][Full Text] [Related]
12. Localization of the cystic fibrosis transmembrane conductance regulator in airway secretory glands.
Jacquot J; Puchelle E; Hinnrasky J; Fuchey C; Bettinger C; Spilmont C; Bonnet N; Dieterle A; Dreyer D; Pavirani A
Eur Respir J; 1993 Feb; 6(2):169-76. PubMed ID: 7680322
[TBL] [Abstract][Full Text] [Related]
13. Gene transduction and cell entry pathway of fiber-modified adenovirus type 5 vectors carrying novel endocytic peptide ligands selected on human tracheal glandular cells.
Gaden F; Franqueville L; Magnusson MK; Hong SS; Merten MD; Lindholm L; Boulanger P
J Virol; 2004 Jul; 78(13):7227-47. PubMed ID: 15194799
[TBL] [Abstract][Full Text] [Related]
14. High-efficiency transfer of cystic fibrosis transmembrane conductance regulator cDNA into cystic fibrosis airway cells in culture using lactosylated polylysine as a vector.
Kollen WJ; Mulberg AE; Wei X; Sugita M; Raghuram V; Wang J; Foskett JK; Glick MC; Scanlin TF
Hum Gene Ther; 1999 Mar; 10(4):615-22. PubMed ID: 10094204
[TBL] [Abstract][Full Text] [Related]
15. Gene transfer to freshly isolated human respiratory epithelial cells in vitro using a replication-deficient adenovirus containing the human cystic fibrosis transmembrane conductance regulator cDNA.
Rosenfeld MA; Chu CS; Seth P; Danel C; Banks T; Yoneyama K; Yoshimura K; Crystal RG
Hum Gene Ther; 1994 Mar; 5(3):331-42. PubMed ID: 7517189
[TBL] [Abstract][Full Text] [Related]
16. CFTR gene transfer reduces the binding of Pseudomonas aeruginosa to cystic fibrosis respiratory epithelium.
Davies JC; Stern M; Dewar A; Caplen NJ; Munkonge FM; Pitt T; Sorgi F; Huang L; Bush A; Geddes DM; Alton EW
Am J Respir Cell Mol Biol; 1997 Jun; 16(6):657-63. PubMed ID: 9191467
[TBL] [Abstract][Full Text] [Related]
17. Serum albumin enhances polyethylenimine-mediated gene delivery to human respiratory epithelial cells.
Carrabino S; Di Gioia S; Copreni E; Conese M
J Gene Med; 2005 Dec; 7(12):1555-64. PubMed ID: 16028303
[TBL] [Abstract][Full Text] [Related]
18. Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium.
Puchelle E; Gaillard D; Ploton D; Hinnrasky J; Fuchey C; Boutterin MC; Jacquot J; Dreyer D; Pavirani A; Dalemans W
Am J Respir Cell Mol Biol; 1992 Nov; 7(5):485-91. PubMed ID: 1384582
[TBL] [Abstract][Full Text] [Related]
19. An immortalized cystic fibrosis tracheal epithelial cell line homozygous for the delta F508 CFTR mutation.
Kunzelmann K; Schwiebert EM; Zeitlin PL; Kuo WL; Stanton BA; Gruenert DC
Am J Respir Cell Mol Biol; 1993 May; 8(5):522-9. PubMed ID: 7683197
[TBL] [Abstract][Full Text] [Related]
20. Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells.
Baconnais S; Delavoie F; Zahm JM; Milliot M; Terryn C; Castillon N; Banchet V; Michel J; Danos O; Merten M; Chinet T; Zierold K; Bonnet N; Puchelle E; Balossier G
Exp Cell Res; 2005 Oct; 309(2):296-304. PubMed ID: 16051214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
