22 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 32712714 | Transport properties in CFTR-/- knockout piglets suggest normal airway surface liquid pH and enhanced amiloride-sensitive Na+ absorption. | 2020 Oct | 2 |
2 | 30272672 | Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD). | 2018 Sep 13 | 1 |
3 | 27941075 | δβγ-ENaC is inhibited by CFTR but stimulated by cAMP in Xenopus laevis oocytes. | 2017 Feb 1 | 1 |
4 | 24105369 | The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells. | 2014 May | 2 |
5 | 23732645 | Increased apical Na+ permeability in cystic fibrosis is supported by a quantitative model of epithelial ion transport. | 2013 Aug 1 | 1 |
6 | 22302997 | Flow cytometry analysis reveals a decrease in intracellular sodium during sperm capacitation. | 2012 Jan 15 | 1 |
7 | 21145458 | Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia. | 2010 Dec 10 | 1 |
8 | 19633071 | Dysfunctional cystic fibrosis transmembrane conductance regulator inhibits phagocytosis of apoptotic cells with proinflammatory consequences. | 2009 Oct | 1 |
9 | 18288363 | Effect of Huoxiang-zhengqi liquid on HCO(3)(-) secretion by intact porcine distal airway epithelium. | 2008 Feb 25 | 1 |
10 | 18309088 | Parallel improvement of sodium and chloride transport defects by miglustat (n-butyldeoxynojyrimicin) in cystic fibrosis epithelial cells. | 2008 Jun | 1 |
11 | 16226002 | ENaC- and CFTR-dependent ion and fluid transport in human middle ear epithelial cells. | 2006 Jan | 1 |
12 | 16714334 | PAR2 activation interrupts E-cadherin adhesion and compromises the airway epithelial barrier: protective effect of beta-agonists. | 2006 Oct | 2 |
13 | 16027156 | Cl- interference with the epithelial Na+ channel ENaC. | 2005 Sep 9 | 1 |
14 | 16463140 | ENaC activity requires CFTR channel function independently of phosphorylation in sweat duct. | 2005 Sep | 2 |
15 | 12177237 | Polarized expression of cystic fibrosis transmembrane conductance regulator and associated epithelial proteins during the regeneration of human airway surface epithelium in three-dimensional culture. | 2002 Aug | 1 |
16 | 10788432 | Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes. | 2000 May 5 | 1 |
17 | 9476862 | A pilot clinical trial of oral sodium 4-phenylbutyrate (Buphenyl) in deltaF508-homozygous cystic fibrosis patients: partial restoration of nasal epithelial CFTR function. | 1998 Feb | 1 |
18 | 9649552 | The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways. | 1998 Jul 1 | 1 |
19 | 9311495 | Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosis. | 1997 Sep | 1 |
20 | 8759925 | Regulation of the CFTR chloride channel from humans and sharks. | 1996 Jul 1 | 1 |
21 | 8967432 | In vivo analysis of fluid transport in cystic fibrosis airway epithelia of bronchial xenografts. | 1996 May | 1 |
22 | 7491973 | Role of CFTR in chloride secretion across human tracheal epithelium. | 1995 Nov | 1 |