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166 related items for PubMed ID: 38573173

  • 1. Pulmonary Ionocytes Regulate Airway Surface Liquid pH in Primary Human Bronchial Epithelial Cells.
    Luan X, Henao Romero N, Campanucci VA, Le Y, Mustofa J, Tam JS, Ianowski JP.
    Am J Respir Crit Care Med; 2024 Sep 15; 210(6):788-800. PubMed ID: 38573173
    [Abstract] [Full Text] [Related]

  • 2. Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis.
    Abou Alaiwa MH, Launspach JL, Grogan B, Carter S, Zabner J, Stoltz DA, Singh PK, McKone EF, Welsh MJ.
    JCI Insight; 2018 Aug 09; 3(15):. PubMed ID: 30089726
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  • 3. Modulator Combination Improves In Vitro the Microrheological Properties of the Airway Surface Liquid of Cystic Fibrosis Airway Epithelia.
    Ludovico A, Moran O, Baroni D.
    Int J Mol Sci; 2022 Sep 27; 23(19):. PubMed ID: 36232697
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  • 5. CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium.
    Zhang L, Button B, Gabriel SE, Burkett S, Yan Y, Skiadopoulos MH, Dang YL, Vogel LN, McKay T, Mengos A, Boucher RC, Collins PL, Pickles RJ.
    PLoS Biol; 2009 Jul 27; 7(7):e1000155. PubMed ID: 19621064
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  • 7. 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 Jul 27; 7(5):e37746. PubMed ID: 22662206
    [Abstract] [Full Text] [Related]

  • 8. Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia.
    Gianotti A, Capurro V, Delpiano L, Mielczarek M, García-Valverde M, Carreira-Barral I, Ludovico A, Fiore M, Baroni D, Moran O, Quesada R, Caci E.
    Int J Mol Sci; 2020 Feb 21; 21(4):. PubMed ID: 32098269
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  • 9. Ursodeoxycholic acid inhibits ENaC and Na/K pump activity to restore airway surface liquid height in cystic fibrosis bronchial epithelial cells.
    Mroz MS, Harvey BJ.
    Steroids; 2019 Nov 21; 151():108461. PubMed ID: 31344409
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  • 11. Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium.
    Coakley RD, Grubb BR, Paradiso AM, Gatzy JT, Johnson LG, Kreda SM, O'Neal WK, Boucher RC.
    Proc Natl Acad Sci U S A; 2003 Dec 23; 100(26):16083-8. PubMed ID: 14668433
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  • 12. Airway submucosal glands from cystic fibrosis swine suffer from abnormal ion transport across the serous acini, collecting duct, and ciliated duct.
    Luan X, Tam JS, Jagadeeshan S, Grishchenko N, Hassan N, Gioino P, Shipley AM, Machen TE, Ianowski JP.
    Am J Physiol Lung Cell Mol Physiol; 2020 May 01; 318(5):L931-L942. PubMed ID: 32130033
    [Abstract] [Full Text] [Related]

  • 13. CFTR-rich ionocytes mediate chloride absorption across airway epithelia.
    Lei L, Traore S, Romano Ibarra GS, Karp PH, Rehman T, Meyerholz DK, Zabner J, Stoltz DA, Sinn PL, Welsh MJ, McCray PB, Thornell IM.
    J Clin Invest; 2023 Oct 16; 133(20):. PubMed ID: 37581935
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  • 15. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties via hydration.
    Morrison CB, Shaffer KM, Araba KC, Markovetz MR, Wykoff JA, Quinney NL, Hao S, Delion MF, Flen AL, Morton LC, Liao J, Hill DB, Drumm ML, O'Neal WK, Kesimer M, Gentzsch M, Ehre C.
    Eur Respir J; 2022 Feb 16; 59(2):. PubMed ID: 34172469
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  • 17. Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770.
    Van Goor F, Hadida S, Grootenhuis PD, Burton B, Cao D, Neuberger T, Turnbull A, Singh A, Joubran J, Hazlewood A, Zhou J, McCartney J, Arumugam V, Decker C, Yang J, Young C, Olson ER, Wine JJ, Frizzell RA, Ashlock M, Negulescu P.
    Proc Natl Acad Sci U S A; 2009 Nov 03; 106(44):18825-30. PubMed ID: 19846789
    [Abstract] [Full Text] [Related]

  • 18. Airway surface liquid homeostasis in cystic fibrosis: pathophysiology and therapeutic targets.
    Haq IJ, Gray MA, Garnett JP, Ward C, Brodlie M.
    Thorax; 2016 Mar 03; 71(3):284-7. PubMed ID: 26719229
    [Abstract] [Full Text] [Related]

  • 19. Secretory Cells Dominate Airway CFTR Expression and Function in Human Airway Superficial Epithelia.
    Okuda K, Dang H, Kobayashi Y, Carraro G, Nakano S, Chen G, Kato T, Asakura T, Gilmore RC, Morton LC, Lee RE, Mascenik T, Yin WN, Barbosa Cardenas SM, O'Neal YK, Minnick CE, Chua M, Quinney NL, Gentzsch M, Anderson CW, Ghio A, Matsui H, Nagase T, Ostrowski LE, Grubb BR, Olsen JC, Randell SH, Stripp BR, Tata PR, O'Neal WK, Boucher RC.
    Am J Respir Crit Care Med; 2021 May 15; 203(10):1275-1289. PubMed ID: 33321047
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  • 20. Automated acquisition and analysis of airway surface liquid height by confocal microscopy.
    Choi HC, Kim CS, Tarran R.
    Am J Physiol Lung Cell Mol Physiol; 2015 Jul 15; 309(2):L109-18. PubMed ID: 26001773
    [Abstract] [Full Text] [Related]

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