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Items: 1 to 20 of 155

1.

CFTR dysfunction induces vascular endothelial growth factor synthesis in airway epithelium.

Martin C, Coolen N, Wu Y, Thévenot G, Touqui L, Prulière-Escabasse V, Papon JF, Coste A, Escudier E, Dusser DJ, Fajac I, Burgel PR.

Eur Respir J. 2013 Dec;42(6):1553-62. doi: 10.1183/09031936.00164212. Epub 2013 Mar 21.

2.

EG-VEGF, BV8, and their receptor expression in human bronchi and their modification in cystic fibrosis: Impact of CFTR mutation (delF508).

Chauvet S, Traboulsi W, Thevenon L, Kouadri A, Feige JJ, Camara B, Alfaidy N, Benharouga M.

Am J Physiol Lung Cell Mol Physiol. 2015 Aug 1;309(3):L314-22. doi: 10.1152/ajplung.00382.2014. Epub 2015 Jun 5.

3.

Improvement of defective cystic fibrosis airway epithelial wound repair after CFTR rescue.

Trinh NT, Bardou O, Privé A, Maillé E, Adam D, Lingée S, Ferraro P, Desrosiers MY, Coraux C, Brochiero E.

Eur Respir J. 2012 Dec;40(6):1390-400. doi: 10.1183/09031936.00221711. Epub 2012 Apr 10.

4.

Pseudomonas aeruginosa induces vascular endothelial growth factor synthesis in airway epithelium in vitro and in vivo.

Martin C, Thévenot G, Danel S, Chapron J, Tazi A, Macey J, Dusser DJ, Fajac I, Burgel PR.

Eur Respir J. 2011 Oct;38(4):939-46. doi: 10.1183/09031936.00134910. Epub 2011 Mar 24.

5.

The CFTR and EGFR relationship in airway vascular growth, and its importance in cystic fibrosis.

Nadel JA.

Eur Respir J. 2013 Dec;42(6):1438-40. doi: 10.1183/09031936.00107513. No abstract available. Erratum in: Eur Respir J. 2014 Feb;43(2):658.

6.

Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation.

Blanchard E, Marie S, Riffault L, Bonora M, Tabary O, Clement A, Jacquot J.

Biochem Biophys Res Commun. 2011 Aug 5;411(3):471-6. doi: 10.1016/j.bbrc.2011.06.104. Epub 2011 Jun 24.

PMID:
21723850
7.

Na+/H+ exchanger regulatory factor isoform 1 overexpression modulates cystic fibrosis transmembrane conductance regulator (CFTR) expression and activity in human airway 16HBE14o- cells and rescues DeltaF508 CFTR functional expression in cystic fibrosis cells.

Guerra L, Fanelli T, Favia M, Riccardi SM, Busco G, Cardone RA, Carrabino S, Weinman EJ, Reshkin SJ, Conese M, Casavola V.

J Biol Chem. 2005 Dec 9;280(49):40925-33. Epub 2005 Oct 3.

8.

Regulation of gap junctional communication by a pro-inflammatory cytokine in cystic fibrosis transmembrane conductance regulator-expressing but not cystic fibrosis airway cells.

Chanson M, Berclaz PY, Scerri I, Dudez T, Wernke-Dollries K, Pizurki L, Pavirani A, Fiedler MA, Suter S.

Am J Pathol. 2001 May;158(5):1775-84.

9.

Normal CFTR inhibits epidermal growth factor receptor-dependent pro-inflammatory chemokine production in human airway epithelial cells.

Kim S, Beyer BA, Lewis C, Nadel JA.

PLoS One. 2013 Aug 16;8(8):e72981. doi: 10.1371/journal.pone.0072981. eCollection 2013.

10.

CFTR induces the expression of DRA along with Cl(-)/HCO(3)(-) exchange activity in tracheal epithelial cells.

Wheat VJ, Shumaker H, Burnham C, Shull GE, Yankaskas JR, Soleimani M.

Am J Physiol Cell Physiol. 2000 Jul;279(1):C62-71.

11.

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.

12.

Biochemical characterization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis epithelial cells.

Sarkadi B, Bauzon D, Huckle WR, Earp HS, Berry A, Suchindran H, Price EM, Olson JC, Boucher RC, Scarborough GA.

J Biol Chem. 1992 Jan 25;267(3):2087-95.

13.

Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.

Oglesby IK, Chotirmall SH, McElvaney NG, Greene CM.

J Immunol. 2013 Apr 1;190(7):3354-62. doi: 10.4049/jimmunol.1202960. Epub 2013 Feb 22.

14.

Cystic fibrosis transmembrane conductance regulator-mRNA delivery: a novel alternative for cystic fibrosis gene therapy.

Bangel-Ruland N, Tomczak K, Fernández Fernández E, Leier G, Leciejewski B, Rudolph C, Rosenecker J, Weber WM.

J Gene Med. 2013 Nov-Dec;15(11-12):414-26. doi: 10.1002/jgm.2748.

PMID:
24123772
15.

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. doi: 10.1165/rcmb.2007-0456OC. Epub 2008 Aug 21.

PMID:
18723440
16.

Transgenic cystic fibrosis mice exhibit reduced early clearance of Pseudomonas aeruginosa from the respiratory tract.

Schroeder TH, Reiniger N, Meluleni G, Grout M, Coleman FT, Pier GB.

J Immunol. 2001 Jun 15;166(12):7410-8.

17.

Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.

LeSimple P, Liao J, Robert R, Gruenert DC, Hanrahan JW.

J Physiol. 2010 Apr 15;588(Pt 8):1195-209. doi: 10.1113/jphysiol.2009.182246. Epub 2010 Feb 15.

18.

Regulated expression of the human CFTR gene in epithelial cells.

Ye L, Chan S, Chow YH, Tsui LC, Hu J.

Mol Ther. 2001 May;3(5 Pt 1):723-33.

19.

Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.

Antigny F, Norez C, Dannhoffer L, Bertrand J, Raveau D, Corbi P, Jayle C, Becq F, Vandebrouck C.

Am J Respir Cell Mol Biol. 2011 Jan;44(1):83-90. doi: 10.1165/rcmb.2009-0347OC. Epub 2010 Mar 4.

PMID:
20203293
20.

Airway epithelial CFTR mRNA expression in cystic fibrosis patients after repetitive administration of a recombinant adenovirus.

Harvey BG, Leopold PL, Hackett NR, Grasso TM, Williams PM, Tucker AL, Kaner RJ, Ferris B, Gonda I, Sweeney TD, Ramalingam R, Kovesdi I, Shak S, Crystal RG.

J Clin Invest. 1999 Nov;104(9):1245-55.

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