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Journal Abstract Search
181 related items for 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 01; 177(3):209-19. PubMed ID: 11014859 [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 12; 279(11):10720-9. PubMed ID: 14701827 [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 01; 548(Pt 1):203-18. PubMed ID: 12562898 [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 05; 285(45):34850-63. PubMed ID: 20739289 [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 Nov 05; 2(4):299-309. PubMed ID: 14719996 [Abstract] [Full Text] [Related]