238 related articles for article (PubMed ID: 10199813)
1. UTP inhibits Na+ absorption in wild-type and DeltaF508 CFTR-expressing human bronchial epithelia.
Devor DC; Pilewski JM
Am J Physiol; 1999 Apr; 276(4):C827-37. PubMed ID: 10199813
[TBL] [Abstract][Full Text] [Related]
2. Pharmacological modulation of ion transport across wild-type and DeltaF508 CFTR-expressing human bronchial epithelia.
Devor DC; Bridges RJ; Pilewski JM
Am J Physiol Cell Physiol; 2000 Aug; 279(2):C461-79. PubMed ID: 10913013
[TBL] [Abstract][Full Text] [Related]
3. Inhibition of amiloride-sensitive epithelial Na(+) absorption by extracellular nucleotides in human normal and cystic fibrosis airways.
Mall M; Wissner A; Gonska T; Calenborn D; Kuehr J; Brandis M; Kunzelmann K
Am J Respir Cell Mol Biol; 2000 Dec; 23(6):755-61. PubMed ID: 11104728
[TBL] [Abstract][Full Text] [Related]
4. Effect of luminal nucleotides on Cl- secretion and Na+ absorption in distal bronchi.
Inglis SK; Collett A; McAlroy HL; Wilson SM; Olver RE
Pflugers Arch; 1999 Oct; 438(5):621-7. PubMed ID: 10555558
[TBL] [Abstract][Full Text] [Related]
5. Extracellular UTP stimulates electrogenic bicarbonate secretion across CFTR knockout gallbladder epithelium.
Clarke LL; Harline MC; Gawenis LR; Walker NM; Turner JT; Weisman GA
Am J Physiol Gastrointest Liver Physiol; 2000 Jul; 279(1):G132-8. PubMed ID: 10898755
[TBL] [Abstract][Full Text] [Related]
6. Na-K-Cl cotransport in nystatin-treated tracheal cells: regulation by isoproterenol, apical UTP, and [Cl]i.
Haas M; McBrayer DG
Am J Physiol; 1994 May; 266(5 Pt 1):C1440-52. PubMed ID: 8203506
[TBL] [Abstract][Full Text] [Related]
7. Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.
Itani OA; Chen JH; Karp PH; Ernst S; Keshavjee S; Parekh K; Klesney-Tait J; Zabner J; Welsh MJ
Proc Natl Acad Sci U S A; 2011 Jun; 108(25):10260-5. PubMed ID: 21646513
[TBL] [Abstract][Full Text] [Related]
8. Hyperabsorption of Na+ and raised Ca(2+)-mediated Cl- secretion in nasal epithelia of CF mice.
Grubb BR; Vick RN; Boucher RC
Am J Physiol; 1994 May; 266(5 Pt 1):C1478-83. PubMed ID: 7515571
[TBL] [Abstract][Full Text] [Related]
9. Mechanisms for the inhibition of amiloride-sensitive Na+ absorption by extracellular nucleotides in mouse trachea.
Kunzelmann K; Schreiber R; Cook D
Pflugers Arch; 2002 May; 444(1-2):220-6. PubMed ID: 11976935
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Minor role of Cl- secretion in non-cystic fibrosis and cystic fibrosis human nasal epithelium.
Rückes-Nilges C; Weber U; Lindemann H; Münker G; Clauss W; Weber WM
Cell Physiol Biochem; 1999; 9(1):1-10. PubMed ID: 10352340
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Effects of purinergic stimulation, CFTR and osmotic stress on amiloride-sensitive Na+ transport in epithelia and Xenopus oocytes.
Schreiber R; König J; Sun J; Markovich D; Kunzelmann K
J Membr Biol; 2003 Mar; 192(2):101-10. PubMed ID: 12682798
[TBL] [Abstract][Full Text] [Related]
15. Sodium channel blockers and uridine triphosphate: effects on nasal potential difference in cystic fibrosis mice.
Ghosal S; Taylor CJ; Colledge WH; Ratcliff R; Evans MJ
Eur Respir J; 2000 Jan; 15(1):146-50. PubMed ID: 10678637
[TBL] [Abstract][Full Text] [Related]
16. SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis.
Grubb BR; Gabriel SE; Mengos A; Gentzsch M; Randell SH; Van Heeckeren AM; Knowles MR; Drumm ML; Riordan JR; Boucher RC
Am J Respir Cell Mol Biol; 2006 Mar; 34(3):355-63. PubMed ID: 16284361
[TBL] [Abstract][Full Text] [Related]
17. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
Johnson LG; Boyles SE; Wilson J; Boucher RC
J Clin Invest; 1995 Mar; 95(3):1377-82. PubMed ID: 7533790
[TBL] [Abstract][Full Text] [Related]
18. CFTR is required for cAMP inhibition of intestinal Na+ absorption in a cystic fibrosis mouse model.
Clarke LL; Harline MC
Am J Physiol; 1996 Feb; 270(2 Pt 1):G259-67. PubMed ID: 8779967
[TBL] [Abstract][Full Text] [Related]
19. Regulation of ion transport via apical purinergic receptors in intact rabbit airway epithelium.
Poulsen AN; Klausen TL; Pedersen PS; Willumsen NJ; Frederiksen O
Pflugers Arch; 2005 Jul; 450(4):227-35. PubMed ID: 15822001
[TBL] [Abstract][Full Text] [Related]
20. Stable knockdown of CFTR establishes a role for the channel in P2Y receptor-stimulated anion secretion.
Palmer ML; Lee SY; Carlson D; Fahrenkrug S; O'Grady SM
J Cell Physiol; 2006 Mar; 206(3):759-70. PubMed ID: 16245306
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
