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Items: 1 to 20 of 72

1.

Activation of airway cl- secretion in human subjects by adenosine.

Hentchel-Franks K, Lozano D, Eubanks-Tarn V, Cobb B, Fan L, Oster R, Sorscher E, Clancy JP.

Am J Respir Cell Mol Biol. 2004 Aug;31(2):140-6. Epub 2004 Mar 23.

PMID:
15039139
2.

Stimulation of chloride secretion by P1 purinoceptor agonists in cystic fibrosis phenotype airway epithelial cell line CFPEo-.

Chao AC, Zifferblatt JB, Wagner JA, Dong YJ, Gruenert DC, Gardner P.

Br J Pharmacol. 1994 May;112(1):169-75.

3.

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.

PMID:
10970817
4.

Adenosine and its nucleotides activate wild-type and R117H CFTR through an A2B receptor-coupled pathway.

Clancy JP, Ruiz FE, Sorscher EJ.

Am J Physiol. 1999 Feb;276(2 Pt 1):C361-9.

6.

Adenosine receptors, cystic fibrosis, and airway hydration.

Com G, Clancy JP.

Handb Exp Pharmacol. 2009;(193):363-81. doi: 10.1007/978-3-540-89615-9_12. Review.

PMID:
19639288
7.

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.

8.

Cystic fibrosis and the relationship between mucin and chloride secretion by cultures of human airway gland mucous cells.

Finkbeiner WE, Zlock LT, Morikawa M, Lao AY, Dasari V, Widdicombe JH.

Am J Physiol Lung Cell Mol Physiol. 2011 Oct;301(4):L402-14. doi: 10.1152/ajplung.00210.2010. Epub 2011 Jul 1.

9.

Calcium-stimulated Cl- secretion in Calu-3 human airway cells requires CFTR.

Moon S, Singh M, Krouse ME, Wine JJ.

Am J Physiol. 1997 Dec;273(6 Pt 1):L1208-19.

10.

DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers.

Rowe SM, Pyle LC, Jurkevante A, Varga K, Collawn J, Sloane PA, Woodworth B, Mazur M, Fulton J, Fan L, Li Y, Fortenberry J, Sorscher EJ, Clancy JP.

Pulm Pharmacol Ther. 2010 Aug;23(4):268-78. doi: 10.1016/j.pupt.2010.02.001. Epub 2010 Mar 10.

11.

Iontophoretic beta-adrenergic stimulation of human sweat glands: possible assay for cystic fibrosis transmembrane conductance regulator activity in vivo.

Shamsuddin AK, Reddy MM, Quinton PM.

Exp Physiol. 2008 Aug;93(8):969-81. doi: 10.1113/expphysiol.2008.042283. Epub 2008 Apr 25.

12.
14.

Isobutylmethylxanthine fails to stimulate chloride secretion in cystic fibrosis airway epithelia.

Grubb B, Lazarowski E, Knowles M, Boucher R.

Am J Respir Cell Mol Biol. 1993 Apr;8(4):454-60.

PMID:
7682824
15.

Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry.

Zsembery A, Fortenberry JA, Liang L, Bebok Z, Tucker TA, Boyce AT, Braunstein GM, Welty E, Bell PD, Sorscher EJ, Clancy JP, Schwiebert EM.

J Biol Chem. 2004 Mar 12;279(11):10720-9. Epub 2003 Dec 29.

16.

Pyridine nucleotide redox potential modulates cystic fibrosis transmembrane conductance regulator Cl- conductance.

Stutts MJ, Gabriel SE, Price EM, Sarkadi B, Olsen JC, Boucher RC.

J Biol Chem. 1994 Mar 25;269(12):8667-74.

17.

A(2) adenosine receptors regulate CFTR through PKA and PLA(2).

Cobb BR, Ruiz F, King CM, Fortenberry J, Greer H, Kovacs T, Sorscher EJ, Clancy JP.

Am J Physiol Lung Cell Mol Physiol. 2002 Jan;282(1):L12-25.

18.

Regulation of membrane chloride currents in rat bile duct epithelial cells.

Fitz JG, Basavappa S, McGill J, Melhus O, Cohn JA.

J Clin Invest. 1993 Jan;91(1):319-28.

19.

Alternate stimulation of apical CFTR by genistein in epithelia.

Illek B, Fischer H, Machen TE.

Am J Physiol. 1996 Jan;270(1 Pt 1):C265-75.

PMID:
8772453
20.

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