Amiloride

CF transmembrane conductance regulator ; Homo sapiens







22 Article(s)
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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