1017 related articles for article (PubMed ID: 19621064)
1. 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]
2. Adenovirus 5-fiber 35 chimeric vector mediates efficient apical correction of the cystic fibrosis transmembrane conductance regulator defect in cystic fibrosis primary airway epithelia.
Granio O; Ashbourne Excoffon KJ; Henning P; Melin P; Norez C; Gonzalez G; Karp PH; Magnusson MK; Habib N; Lindholm L; Becq F; Boulanger P; Zabner J; Hong SS
Hum Gene Ther; 2010 Mar; 21(3):251-69. PubMed ID: 19788389
[TBL] [Abstract][Full Text] [Related]
3. Respiratory syncytial virus engineered to express the cystic fibrosis transmembrane conductance regulator corrects the bioelectric phenotype of human cystic fibrosis airway epithelium in vitro.
Kwilas AR; Yednak MA; Zhang L; Liesman R; Collins PL; Pickles RJ; Peeples ME
J Virol; 2010 Aug; 84(15):7770-81. PubMed ID: 20504917
[TBL] [Abstract][Full Text] [Related]
4. Vector-specific complementation profiles of two independent primary defects in cystic fibrosis airways.
Zhang Y; Jiang Q; Dudus L; Yankaskas JR; Engelhardt JF
Hum Gene Ther; 1998 Mar; 9(5):635-48. PubMed ID: 9551612
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Airway submucosal glands from cystic fibrosis swine suffer from abnormal ion transport across the serous acini, collecting duct, and ciliated duct.
Luan X; Tam JS; Jagadeeshan S; Grishchenko N; Hassan N; Gioino P; Shipley AM; Machen TE; Ianowski JP
Am J Physiol Lung Cell Mol Physiol; 2020 May; 318(5):L931-L942. PubMed ID: 32130033
[TBL] [Abstract][Full Text] [Related]
7. Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia.
Gianotti A; Capurro V; Delpiano L; Mielczarek M; García-Valverde M; Carreira-Barral I; Ludovico A; Fiore M; Baroni D; Moran O; Quesada R; Caci E
Int J Mol Sci; 2020 Feb; 21(4):. PubMed ID: 32098269
[TBL] [Abstract][Full Text] [Related]
8. The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.
Varelogianni G; Hussain R; Strid H; Oliynyk I; Roomans GM; Johannesson M
Cell Biol Int; 2013 Nov; 37(11):1149-56. PubMed ID: 23765701
[TBL] [Abstract][Full Text] [Related]
9. Ursodeoxycholic acid inhibits ENaC and Na/K pump activity to restore airway surface liquid height in cystic fibrosis bronchial epithelial cells.
Mroz MS; Harvey BJ
Steroids; 2019 Nov; 151():108461. PubMed ID: 31344409
[TBL] [Abstract][Full Text] [Related]
10. Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.
Carbone A; Castellani S; Favia M; Diana A; Paracchini V; Di Gioia S; Seia M; Casavola V; Colombo C; Conese M
J Cell Mol Med; 2014 Aug; 18(8):1631-43. PubMed ID: 24894806
[TBL] [Abstract][Full Text] [Related]
11. Airway epithelial cells--hyperabsorption in CF?
Kunzelmann K; Schreiber R
Int J Biochem Cell Biol; 2012 Aug; 44(8):1232-5. PubMed ID: 22542896
[TBL] [Abstract][Full Text] [Related]
12. Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.
Gianotti A; Melani R; Caci E; Sondo E; Ravazzolo R; Galietta LJ; Zegarra-Moran O
Am J Respir Cell Mol Biol; 2013 Sep; 49(3):445-52. PubMed ID: 23600628
[TBL] [Abstract][Full Text] [Related]
13. An integrated mathematical epithelial cell model for airway surface liquid regulation by mechanical forces.
Wu D; Boucher RC; Button B; Elston T; Lin CL
J Theor Biol; 2018 Feb; 438():34-45. PubMed ID: 29154907
[TBL] [Abstract][Full Text] [Related]
14. Anoctamin 1 dysregulation alters bronchial epithelial repair in cystic fibrosis.
Ruffin M; Voland M; Marie S; Bonora M; Blanchard E; Blouquit-Laye S; Naline E; Puyo P; Le Rouzic P; Guillot L; Corvol H; Clement A; Tabary O
Biochim Biophys Acta; 2013 Dec; 1832(12):2340-51. PubMed ID: 24080196
[TBL] [Abstract][Full Text] [Related]
15. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
Johnson LG; Boyles SE; Wilson J; Boucher RC
J Clin Invest; 1995 Mar; 95(3):1377-82. PubMed ID: 7533790
[TBL] [Abstract][Full Text] [Related]
16. Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis.
Abou Alaiwa MH; Launspach JL; Grogan B; Carter S; Zabner J; Stoltz DA; Singh PK; McKone EF; Welsh MJ
JCI Insight; 2018 Aug; 3(15):. PubMed ID: 30089726
[TBL] [Abstract][Full Text] [Related]
17. Generation of novel AAV variants by directed evolution for improved CFTR delivery to human ciliated airway epithelium.
Li W; Zhang L; Johnson JS; Zhijian W; Grieger JC; Ping-Jie X; Drouin LM; Agbandje-McKenna M; Pickles RJ; Samulski RJ
Mol Ther; 2009 Dec; 17(12):2067-77. PubMed ID: 19603002
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Induction of a cAMP-stimulated chloride secretion in regenerating poorly differentiated airway epithelial cells by adenovirus-mediated CFTR gene transfer.
Dupuit F; Chinet T; Zahm JM; Pierrot D; Hinnrasky J; Kaplan H; Bonnet N; Puchelle E
Hum Gene Ther; 1997 Aug; 8(12):1439-50. PubMed ID: 9287144
[TBL] [Abstract][Full Text] [Related]
20. Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency.
Woodworth BA
Laryngoscope; 2015 Oct; 125 Suppl 7(0 7):S1-S13. PubMed ID: 25946147
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
