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Journal Abstract Search

169 related items for PubMed ID: 10952679

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  • 3. Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epithelia.
    Mall M, Wissner A, Schreiber R, Kuehr J, Seydewitz HH, Brandis M, Greger R, Kunzelmann K.
    Am J Respir Cell Mol Biol; 2000 Sep; 23(3):283-9. PubMed ID: 10970817
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  • 5. Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes.
    Suaud L, Carattino M, Kleyman TR, Rubenstein RC.
    J Biol Chem; 2002 Dec 27; 277(52):50341-7. PubMed ID: 12386156
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  • 7. Pharmacological modulation of ion transport across wild-type and DeltaF508 CFTR-expressing human bronchial epithelia.
    Devor DC, Bridges RJ, Pilewski JM.
    Am J Physiol Cell Physiol; 2000 Aug 27; 279(2):C461-79. PubMed ID: 10913013
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  • 8. The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients.
    Roth EK, Hirtz S, Duerr J, Wenning D, Eichler I, Seydewitz HH, Amaral MD, Mall MA.
    PLoS One; 2011 Aug 27; 6(8):e24445. PubMed ID: 21909392
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  • 9. Differential activation of the HCO(3)(-) conductance through the cystic fibrosis transmembrane conductance regulator anion channel by genistein and forskolin in murine duodenum.
    Tuo B, Wen G, Seidler U.
    Br J Pharmacol; 2009 Nov 27; 158(5):1313-21. PubMed ID: 19788494
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  • 11. Wild type but not deltaF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes.
    Mall M, Hipper A, Greger R, Kunzelmann K.
    FEBS Lett; 1996 Feb 26; 381(1-2):47-52. PubMed ID: 8641437
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  • 12. CFTR induces extracellular acid sensing in Xenopus oocytes which activates endogenous Ca²⁺-activated Cl⁻ conductance.
    Kongsuphol P, Schreiber R, Kraidith K, Kunzelmann K.
    Pflugers Arch; 2011 Sep 26; 462(3):479-87. PubMed ID: 21647592
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  • 15. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
    Mall M, Bleich M, Greger R, Schreiber R, Kunzelmann K.
    J Clin Invest; 1998 Jul 01; 102(1):15-21. PubMed ID: 9649552
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  • 16. Inhibition of amiloride-sensitive epithelial Na(+) absorption by extracellular nucleotides in human normal and cystic fibrosis airways.
    Mall M, Wissner A, Gonska T, Calenborn D, Kuehr J, Brandis M, Kunzelmann K.
    Am J Respir Cell Mol Biol; 2000 Dec 01; 23(6):755-61. PubMed ID: 11104728
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  • 17. Effects of the serine/threonine kinase SGK1 on the epithelial Na(+) channel (ENaC) and CFTR: implications for cystic fibrosis.
    Wagner CA, Ott M, Klingel K, Beck S, Melzig J, Friedrich B, Wild KN, Bröer S, Moschen I, Albers A, Waldegger S, Tümmler B, Egan ME, Geibel JP, Kandolf R, Lang F.
    Cell Physiol Biochem; 2001 Dec 01; 11(4):209-18. PubMed ID: 11509829
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  • 18. Abnormal regulatory interactions of I148T-CFTR and the epithelial Na+ channel in Xenopus oocytes.
    Suaud L, Yan W, Rubenstein RC.
    Am J Physiol Cell Physiol; 2007 Jan 01; 292(1):C603-11. PubMed ID: 16822950
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  • 19. Mechanosensitive activation of CFTR by increased cell volume and hydrostatic pressure but not shear stress.
    Vitzthum C, Clauss WG, Fronius M.
    Biochim Biophys Acta; 2015 Nov 01; 1848(11 Pt A):2942-51. PubMed ID: 26357939
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  • 20. No evidence for direct activation of the cystic fibrosis transmembrane conductance regulator by 8-cyclopentyl-1,3-dipropylxanthine.
    Kunzelmann K, Briel M, Schreiber R, Ricken S, Nitschke R, Greger R.
    Cell Physiol Biochem; 1998 Nov 01; 8(4):185-93. PubMed ID: 9694345
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