185 related articles for article (PubMed ID: 11014859)
1. CFTR regulation of intracellular calcium in normal and cystic fibrosis human airway epithelia.
Walsh DE; Harvey BJ; Urbach V
J Membr Biol; 2000 Oct; 177(3):209-19. PubMed ID: 11014859
[TBL] [Abstract][Full Text] [Related]
2. 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; 279(11):10720-9. PubMed ID: 14701827
[TBL] [Abstract][Full Text] [Related]
3. cAMP and genistein stimulate HCO3- conductance through CFTR in human airway epithelia.
Illek B; Yankaskas JR; Machen TE
Am J Physiol; 1997 Apr; 272(4 Pt 1):L752-61. PubMed ID: 9142951
[TBL] [Abstract][Full Text] [Related]
4. Polarized signaling via purinoceptors in normal and cystic fibrosis airway epithelia.
Paradiso AM; Ribeiro CM; Boucher RC
J Gen Physiol; 2001 Jan; 117(1):53-67. PubMed ID: 11134231
[TBL] [Abstract][Full Text] [Related]
5. Purinoceptor activation of chloride transport in cystic fibrosis and CFTR-transfected pancreatic cell lines.
O'Reilly CM; O'Farrell AM; Ryan MP
Br J Pharmacol; 1998 Aug; 124(8):1597-606. PubMed ID: 9756374
[TBL] [Abstract][Full Text] [Related]
6. Regulation of intracellular Ca(2+) by CFTR in Chinese hamster ovary cells.
Urbach V; Harvey BJ
J Membr Biol; 1999 Oct; 171(3):255-65. PubMed ID: 10501833
[TBL] [Abstract][Full Text] [Related]
7. Role of the cystic fibrosis transmembrane conductance channel in human airway smooth muscle.
Michoud MC; Robert R; Hassan M; Moynihan B; Haston C; Govindaraju V; Ferraro P; Hanrahan JW; Martin JG
Am J Respir Cell Mol Biol; 2009 Feb; 40(2):217-22. PubMed ID: 18757309
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 17339840
[TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis airway epithelial Ca2+ i signaling: the mechanism for the larger agonist-mediated Ca2+ i signals in human cystic fibrosis airway epithelia.
Ribeiro CM; Paradiso AM; Carew MA; Shears SB; Boucher RC
J Biol Chem; 2005 Mar; 280(11):10202-9. PubMed ID: 15647273
[TBL] [Abstract][Full Text] [Related]
10. Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
Paradiso AM; Coakley RD; Boucher RC
J Physiol; 2003 Apr; 548(Pt 1):203-18. PubMed ID: 12562898
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 20203293
[TBL] [Abstract][Full Text] [Related]
12. 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; 285(45):34850-63. PubMed ID: 20739289
[TBL] [Abstract][Full Text] [Related]
13. Pharmacotherapy of the ion transport defect in cystic fibrosis: role of purinergic receptor agonists and other potential therapeutics.
Kunzelmann K; Mall M
Am J Respir Med; 2003; 2(4):299-309. PubMed ID: 14719996
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. ATP release triggered by activation of the Ca2+-activated K+ channel in human airway Calu-3 cells.
Ito Y; Son M; Sato S; Ishikawa T; Kondo M; Nakayama S; Shimokata K; Kume H
Am J Respir Cell Mol Biol; 2004 Mar; 30(3):388-95. PubMed ID: 12947021
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 20226262
[TBL] [Abstract][Full Text] [Related]
18. Purinergic regulation of CFTR and Ca(2+)-activated Cl(-) channels and K(+) channels in human pancreatic duct epithelium.
Wang J; Haanes KA; Novak I
Am J Physiol Cell Physiol; 2013 Apr; 304(7):C673-84. PubMed ID: 23364268
[TBL] [Abstract][Full Text] [Related]
19. Cystic fibrosis transmembrane regulator-independent release of ATP. Its implications for the regulation of P2Y2 receptors in airway epithelia.
Watt WC; Lazarowski ER; Boucher RC
J Biol Chem; 1998 May; 273(22):14053-8. PubMed ID: 9593757
[TBL] [Abstract][Full Text] [Related]
20. Basal nucleotide levels, release, and metabolism in normal and cystic fibrosis airways.
Donaldson SH; Lazarowski ER; Picher M; Knowles MR; Stutts MJ; Boucher RC
Mol Med; 2000 Nov; 6(11):969-82. PubMed ID: 11147574
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
