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Results: 1 to 20 of 92

1.

H2O2 stimulates cystic fibrosis transmembrane conductance regulator through an autocrine prostaglandin pathway, using multidrug-resistant protein-4.

Conner GE, Ivonnet P, Gelin M, Whitney P, Salathe M.

Am J Respir Cell Mol Biol. 2013 Oct;49(4):672-9. doi: 10.1165/rcmb.2013-0156OC.

PMID:
23742099
[PubMed - indexed for MEDLINE]
2.

Cystic fibrosis transmembrane conductance regulator activation by roflumilast contributes to therapeutic benefit in chronic bronchitis.

Lambert JA, Raju SV, Tang LP, McNicholas CM, Li Y, Courville CA, Farris RF, Coricor GE, Smoot LH, Mazur MM, Dransfield MT, Bolger GB, Rowe SM.

Am J Respir Cell Mol Biol. 2014 Mar;50(3):549-58. doi: 10.1165/rcmb.2013-0228OC.

PMID:
24106801
[PubMed - indexed for MEDLINE]
3.

Prostaglandin E₂regulation of cystic fibrosis transmembrane conductance regulator activity and airway surface liquid volume requires gap junctional communication.

Scheckenbach KE, Losa D, Dudez T, Bacchetta M, O'Grady S, Crespin S, Chanson M.

Am J Respir Cell Mol Biol. 2011 Jan;44(1):74-82. doi: 10.1165/rcmb.2009-0361OC. Epub 2010 Feb 18.

PMID:
20167933
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Adenosine regulation of cystic fibrosis transmembrane conductance regulator through prostenoids in airway epithelia.

Li Y, Wang W, Parker W, Clancy JP.

Am J Respir Cell Mol Biol. 2006 May;34(5):600-8. Epub 2006 Jan 6.

PMID:
16399952
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

The prostaglandin E₂ type 4 receptor participates in the response to acute oxidant stress in airway epithelial cells.

Jones CL, Li T, Cowley EA.

J Pharmacol Exp Ther. 2012 May;341(2):552-63. doi: 10.1124/jpet.111.187138. Epub 2012 Feb 23.

PMID:
22362924
[PubMed - indexed for MEDLINE]
Free Article
6.
7.

Compartmentalized autocrine signaling to cystic fibrosis transmembrane conductance regulator at the apical membrane of airway epithelial cells.

Huang P, Lazarowski ER, Tarran R, Milgram SL, Boucher RC, Stutts MJ.

Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):14120-5. Epub 2001 Nov 13.

PMID:
11707576
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Lubiprostone targets prostanoid EP₄ receptors in ovine airways.

Cuthbert AW.

Br J Pharmacol. 2011 Jan;162(2):508-20. doi: 10.1111/j.1476-5381.2010.01058.x.

PMID:
20883477
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

S-Nitrosothiols increases cystic fibrosis transmembrane regulator expression and maturation in the cell surface.

Zaman K, Bennett D, Fraser-Butler M, Greenberg Z, Getsy P, Sattar A, Smith L, Corey D, Sun F, Hunt J, Lewis SJ, Gaston B.

Biochem Biophys Res Commun. 2014 Jan 24;443(4):1257-62. doi: 10.1016/j.bbrc.2013.12.130. Epub 2014 Jan 3.

PMID:
24393850
[PubMed - indexed for MEDLINE]
10.

Apical adenosine regulates basolateral Ca2+-activated potassium channels in human airway Calu-3 epithelial cells.

Wang D, Sun Y, Zhang W, Huang P.

Am J Physiol Cell Physiol. 2008 Jun;294(6):C1443-53. doi: 10.1152/ajpcell.00556.2007. Epub 2008 Apr 2.

PMID:
18385283
[PubMed - indexed for MEDLINE]
Free Article
11.

Cystic fibrosis transmembrane conductance regulator can export hyaluronan.

Schulz T, Schumacher U, Prante C, Sextro W, Prehm P.

Pathobiology. 2010;77(4):200-9. doi: 10.1159/000295859. Epub 2010 Jul 7.

PMID:
20616615
[PubMed - indexed for MEDLINE]
Free Article
12.

CFTR channels in immortalized human airway cells.

Haws C, Krouse ME, Xia Y, Gruenert DC, Wine JJ.

Am J Physiol. 1992 Dec;263(6 Pt 1):L692-707.

PMID:
1282304
[PubMed - indexed for MEDLINE]
13.

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.

PMID:
16203733
[PubMed - indexed for MEDLINE]
Free Article
14.

Lubiprostone targets prostanoid signaling and promotes ion transporter trafficking, mucus exocytosis, and contractility.

Jakab RL, Collaco AM, Ameen NA.

Dig Dis Sci. 2012 Nov;57(11):2826-45. doi: 10.1007/s10620-012-2352-8. Epub 2012 Aug 25.

PMID:
22923315
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Chloride transporting capability of Calu-3 epithelia following persistent knockdown of the cystic fibrosis transmembrane conductance regulator, CFTR.

MacVinish LJ, Cope G, Ropenga A, Cuthbert AW.

Br J Pharmacol. 2007 Apr;150(8):1055-65. Epub 2007 Mar 5.

PMID:
17339840
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Activation of the cystic fibrosis transmembrane conductance regulator by the flavonoid quercetin: potential use as a biomarker of ΔF508 cystic fibrosis transmembrane conductance regulator rescue.

Pyle LC, Fulton JC, Sloane PA, Backer K, Mazur M, Prasain J, Barnes S, Clancy JP, Rowe SM.

Am J Respir Cell Mol Biol. 2010 Nov;43(5):607-16. doi: 10.1165/rcmb.2009-0281OC. Epub 2009 Dec 30.

PMID:
20042712
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.

Swiatecka-Urban A, Brown A, Moreau-Marquis S, Renuka J, Coutermarsh B, Barnaby R, Karlson KH, Flotte TR, Fukuda M, Langford GM, Stanton BA.

J Biol Chem. 2005 Nov 4;280(44):36762-72. Epub 2005 Aug 30.

PMID:
16131493
[PubMed - indexed for MEDLINE]
Free Article
19.

Pseudomonas aeruginosa Homoserine lactone activates store-operated cAMP and cystic fibrosis transmembrane regulator-dependent Cl- secretion by human airway epithelia.

Schwarzer C, Wong S, Shi J, Matthes E, Illek B, Ianowski JP, Arant RJ, Isacoff E, Vais H, Foskett JK, Maiellaro I, Hofer AM, Machen TE.

J Biol Chem. 2010 Nov 5;285(45):34850-63. doi: 10.1074/jbc.M110.167668. Epub 2010 Aug 25.

PMID:
20739289
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia.

Veit G, Bossard F, Goepp J, Verkman AS, Galietta LJ, Hanrahan JW, Lukacs GL.

Mol Biol Cell. 2012 Nov;23(21):4188-202. doi: 10.1091/mbc.E12-06-0424. Epub 2012 Sep 12.

PMID:
22973054
[PubMed - indexed for MEDLINE]
Free PMC Article

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