1262 related articles for article (PubMed ID: 24080196)
21. 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]
22. 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]
23. miR-16 rescues F508del-CFTR function in native cystic fibrosis epithelial cells.
Kumar P; Bhattacharyya S; Peters KW; Glover ML; Sen A; Cox RT; Kundu S; Caohuy H; Frizzell RA; Pollard HB; Biswas R
Gene Ther; 2015 Nov; 22(11):908-16. PubMed ID: 26133785
[TBL] [Abstract][Full Text] [Related]
24. Anoctamin 1 induces calcium-activated chloride secretion and proliferation of renal cyst-forming epithelial cells.
Buchholz B; Faria D; Schley G; Schreiber R; Eckardt KU; Kunzelmann K
Kidney Int; 2014 May; 85(5):1058-67. PubMed ID: 24152967
[TBL] [Abstract][Full Text] [Related]
25. Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.
Tomati V; Caci E; Ferrera L; Pesce E; Sondo E; Cholon DM; Quinney NL; Boyles SE; Armirotti A; Ravazzolo R; Galietta LJ; Gentzsch M; Pedemonte N
JCI Insight; 2018 Feb; 3(3):. PubMed ID: 29415893
[TBL] [Abstract][Full Text] [Related]
26. Abnormal spatial diffusion of Ca2+ in F508del-CFTR airway epithelial cells.
Antigny F; Norez C; Cantereau A; Becq F; Vandebrouck C
Respir Res; 2008 Oct; 9(1):70. PubMed ID: 18973672
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epithelia.
Mall M; Wissner A; Schreiber R; Kuehr J; Seydewitz HH; Brandis M; Greger R; Kunzelmann K
Am J Respir Cell Mol Biol; 2000 Sep; 23(3):283-9. PubMed ID: 10970817
[TBL] [Abstract][Full Text] [Related]
29. TLR-4-mediated innate immunity is reduced in cystic fibrosis airway cells.
John G; Yildirim AO; Rubin BK; Gruenert DC; Henke MO
Am J Respir Cell Mol Biol; 2010 Apr; 42(4):424-31. PubMed ID: 19502387
[TBL] [Abstract][Full Text] [Related]
30. Lipoxin A4 stimulates calcium-activated chloride currents and increases airway surface liquid height in normal and cystic fibrosis airway epithelia.
Verrière V; Higgins G; Al-Alawi M; Costello RW; McNally P; Chiron R; Harvey BJ; Urbach V
PLoS One; 2012; 7(5):e37746. PubMed ID: 22662206
[TBL] [Abstract][Full Text] [Related]
31. Partial correction of endogenous DeltaF508 CFTR in human cystic fibrosis airway epithelia by spliceosome-mediated RNA trans-splicing.
Liu X; Jiang Q; Mansfield SG; Puttaraju M; Zhang Y; Zhou W; Cohn JA; Garcia-Blanco MA; Mitchell LG; Engelhardt JF
Nat Biotechnol; 2002 Jan; 20(1):47-52. PubMed ID: 11753361
[TBL] [Abstract][Full Text] [Related]
32. Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia.
Mall M; Gonska T; Thomas J; Schreiber R; Seydewitz HH; Kuehr J; Brandis M; Kunzelmann K
Pediatr Res; 2003 Apr; 53(4):608-18. PubMed ID: 12612194
[TBL] [Abstract][Full Text] [Related]
33. Epithelial sodium channel inhibition in primary human bronchial epithelia by transfected siRNA.
Caci E; Melani R; Pedemonte N; Yueksekdag G; Ravazzolo R; Rosenecker J; Galietta LJ; Zegarra-Moran O
Am J Respir Cell Mol Biol; 2009 Feb; 40(2):211-6. PubMed ID: 18723440
[TBL] [Abstract][Full Text] [Related]
34. Spiperone, identified through compound screening, activates calcium-dependent chloride secretion in the airway.
Liang L; MacDonald K; Schwiebert EM; Zeitlin PL; Guggino WB
Am J Physiol Cell Physiol; 2009 Jan; 296(1):C131-41. PubMed ID: 18987251
[TBL] [Abstract][Full Text] [Related]
35. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.
Dray-Charier N; Paul A; Scoazec JY; Veissière D; Mergey M; Capeau J; Soubrane O; Housset C
Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100
[TBL] [Abstract][Full Text] [Related]
36. Plasma membrane-localized TMEM16 proteins are indispensable for expression of CFTR.
Benedetto R; Ousingsawat J; Cabrita I; Pinto M; Lérias JR; Wanitchakool P; Schreiber R; Kunzelmann K
J Mol Med (Berl); 2019 May; 97(5):711-722. PubMed ID: 30915480
[TBL] [Abstract][Full Text] [Related]
37. Inflammation in cystic fibrosis airways: relationship to increased bacterial adherence.
Scheid P; Kempster L; Griesenbach U; Davies JC; Dewar A; Weber PP; Colledge WH; Evans MJ; Geddes DM; Alton EW
Eur Respir J; 2001 Jan; 17(1):27-35. PubMed ID: 11307750
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. Purinergic signaling underlies CFTR control of human airway epithelial cell volume.
Braunstein GM; Zsembery A; Tucker TA; Schwiebert EM
J Cyst Fibros; 2004 Jun; 3(2):99-117. PubMed ID: 15463893
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
