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Journal Abstract Search

192 related items for PubMed ID: 26911344

  • 1. The extracellular calcium-sensing receptor regulates human fetal lung development via CFTR.
    Brennan SC, Wilkinson WJ, Tseng HE, Finney B, Monk B, Dibble H, Quilliam S, Warburton D, Galietta LJ, Kemp PJ, Riccardi D.
    Sci Rep; 2016 Feb 25; 6():21975. PubMed ID: 26911344
    [Abstract] [Full Text] [Related]

  • 2. Glucocorticoids Distinctively Modulate the CFTR Channel with Possible Implications in Lung Development and Transition into Extrauterine Life.
    Laube M, Bossmann M, Thome UH.
    PLoS One; 2015 Feb 25; 10(4):e0124833. PubMed ID: 25910246
    [Abstract] [Full Text] [Related]

  • 3. Cystic fibrosis transmembrane conductance regulator (CFTR) dependent cytoskeletal tension during lung organogenesis.
    Cohen JC, Larson JE.
    Dev Dyn; 2006 Oct 25; 235(10):2736-48. PubMed ID: 16906518
    [Abstract] [Full Text] [Related]

  • 4. An exon 5-less splice variant of the extracellular calcium-sensing receptor rescues absence of the full-length receptor in the developing mouse lung.
    Finney B, Wilkinson WJ, Searchfield L, Cole M, Bailey S, Kemp PJ, Riccardi D.
    Exp Lung Res; 2011 Jun 25; 37(5):269-78. PubMed ID: 21352089
    [Abstract] [Full Text] [Related]

  • 5. Calcium-sensing receptor stimulates Cl(-)- and SCFA-dependent but inhibits cAMP-dependent HCO3(-) secretion in colon.
    Tang L, Peng M, Liu L, Chang W, Binder HJ, Cheng SX.
    Am J Physiol Gastrointest Liver Physiol; 2015 May 15; 308(10):G874-83. PubMed ID: 25792563
    [Abstract] [Full Text] [Related]

  • 6. Expression of CFTR and a cAMP-stimulated chloride secretory current in cultured human fetal alveolar epithelial cells.
    McCray PB, Bettencourt JD, Bastacky J, Denning GM, Welsh MJ.
    Am J Respir Cell Mol Biol; 1993 Dec 15; 9(6):578-85. PubMed ID: 7504926
    [Abstract] [Full Text] [Related]

  • 7. F508del-CFTR increases intracellular Ca(2+) signaling that causes enhanced calcium-dependent Cl(-) conductance in cystic fibrosis.
    Martins JR, Kongsuphol P, Sammels E, Dahimène S, Aldehni F, Clarke LA, Schreiber R, de Smedt H, Amaral MD, Kunzelmann K.
    Biochim Biophys Acta; 2011 Nov 15; 1812(11):1385-92. PubMed ID: 21907281
    [Abstract] [Full Text] [Related]

  • 8. Activation of apical CFTR and basolateral Ca(2+)-activated K+ channels by tetramethylpyrazine in Caco-2 cell line.
    Zhu JX, Zhang GH, Yang N, Rowlands DK, Wong HY, Tsang LL, Chung YW, Chan HC.
    Eur J Pharmacol; 2005 Mar 14; 510(3):187-95. PubMed ID: 15763242
    [Abstract] [Full Text] [Related]

  • 9. Fetal lung epithelial ion channels relocate in the cell membrane during late gestation.
    Beard LL, Li T, Hu Y, Folkesson HG.
    Anat Rec (Hoboken); 2011 Sep 14; 294(9):1461-71. PubMed ID: 21809453
    [Abstract] [Full Text] [Related]

  • 10. Molecular mechanisms of calcium-sensing receptor-mediated calcium signaling in the modulation of epithelial ion transport and bicarbonate secretion.
    Xie R, Dong X, Wong C, Vallon V, Tang B, Sun J, Yang S, Dong H.
    J Biol Chem; 2014 Dec 12; 289(50):34642-53. PubMed ID: 25331955
    [Abstract] [Full Text] [Related]

  • 11. Bestrophin and TMEM16-Ca(2+) activated Cl(-) channels with different functions.
    Kunzelmann K, Kongsuphol P, Aldehni F, Tian Y, Ousingsawat J, Warth R, Schreiber R.
    Cell Calcium; 2009 Oct 12; 46(4):233-41. PubMed ID: 19783045
    [Abstract] [Full Text] [Related]

  • 12. ClC and CFTR chloride channel gating.
    Foskett JK.
    Annu Rev Physiol; 1998 Oct 12; 60():689-717. PubMed ID: 9558482
    [Abstract] [Full Text] [Related]

  • 13. Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct.
    Lu M, Dong K, Egan ME, Giebisch GH, Boulpaep EL, Hebert SC.
    Proc Natl Acad Sci U S A; 2010 Mar 30; 107(13):6082-7. PubMed ID: 20231442
    [Abstract] [Full Text] [Related]

  • 14. Localization of cystic fibrosis transmembrane conductance regulator mRNA in human fetal lung tissue by in situ hybridization.
    McCray PB, Wohlford-Lenane CL, Snyder JM.
    J Clin Invest; 1992 Aug 30; 90(2):619-25. PubMed ID: 1379613
    [Abstract] [Full Text] [Related]

  • 15. Bioelectric properties of chloride channels in human, pig, ferret, and mouse airway epithelia.
    Liu X, Luo M, Zhang L, Ding W, Yan Z, Engelhardt JF.
    Am J Respir Cell Mol Biol; 2007 Mar 30; 36(3):313-23. PubMed ID: 17008635
    [Abstract] [Full Text] [Related]

  • 16. Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents.
    Cai Z, Lansdell KA, Sheppard DN.
    Br J Pharmacol; 1999 Sep 30; 128(1):108-18. PubMed ID: 10498841
    [Abstract] [Full Text] [Related]

  • 17. Chloride transporting capability of Calu-3 epithelia following persistent knockdown of the cystic fibrosis transmembrane conductance regulator, CFTR.
    MacVinish LJ, Cope G, Ropenga A, Cuthbert AW.
    Br J Pharmacol; 2007 Apr 30; 150(8):1055-65. PubMed ID: 17339840
    [Abstract] [Full Text] [Related]

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  • 20. Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency.
    Woodworth BA.
    Laryngoscope; 2015 Oct 30; 125 Suppl 7(0 7):S1-S13. PubMed ID: 25946147
    [Abstract] [Full Text] [Related]

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