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166 related items for PubMed ID: 8755664

  • 1. Activation of endogenous deltaF508 cystic fibrosis transmembrane conductance regulator by phosphodiesterase inhibition.
    Kelley TJ, Al-Nakkash L, Cotton CU, Drumm ML.
    J Clin Invest; 1996 Jul 15; 98(2):513-20. PubMed ID: 8755664
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  • 2. C-type natriuretic peptide increases chloride permeability in normal and cystic fibrosis airway cells.
    Kelley TJ, Al-Nakkash L, Drumm ML.
    Am J Respir Cell Mol Biol; 1997 Apr 15; 16(4):464-70. PubMed ID: 9115758
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  • 3. The in vivo effects of milrinone on the airways of cystic fibrosis mice and human subjects.
    Smith SN, Middleton PG, Chadwick S, Jaffe A, Bush KA, Rolleston S, Farley R, Delaney SJ, Wainwright B, Geddes DM, Alton EW.
    Am J Respir Cell Mol Biol; 1999 Jan 15; 20(1):129-34. PubMed ID: 9870926
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  • 4. Activation of wild-type and deltaF508-CFTR by phosphodiesterase inhibitors through cAMP-dependent and -independent mechanisms.
    Al-Nakkash L, Hwang TC.
    Pflugers Arch; 1999 Mar 15; 437(4):553-61. PubMed ID: 10089568
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  • 5. Base treatment corrects defects due to misfolding of mutant cystic fibrosis transmembrane conductance regulator.
    Namkung W, Kim KH, Lee MG.
    Gastroenterology; 2005 Dec 15; 129(6):1979-90. PubMed ID: 16344066
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  • 7. In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium.
    Kelley TJ, Thomas K, Milgram LJ, Drumm ML.
    Proc Natl Acad Sci U S A; 1997 Mar 18; 94(6):2604-8. PubMed ID: 9122242
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  • 8. Regulation of membrane chloride currents in rat bile duct epithelial cells.
    Fitz JG, Basavappa S, McGill J, Melhus O, Cohn JA.
    J Clin Invest; 1993 Jan 18; 91(1):319-28. PubMed ID: 7678606
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  • 9. DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers.
    Rowe SM, Pyle LC, Jurkevante A, Varga K, Collawn J, Sloane PA, Woodworth B, Mazur M, Fulton J, Fan L, Li Y, Fortenberry J, Sorscher EJ, Clancy JP.
    Pulm Pharmacol Ther; 2010 Aug 18; 23(4):268-78. PubMed ID: 20226262
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  • 10. Activation of the cystic fibrosis transmembrane conductance regulator by the flavonoid quercetin: potential use as a biomarker of ΔF508 cystic fibrosis transmembrane conductance regulator rescue.
    Pyle LC, Fulton JC, Sloane PA, Backer K, Mazur M, Prasain J, Barnes S, Clancy JP, Rowe SM.
    Am J Respir Cell Mol Biol; 2010 Nov 18; 43(5):607-16. PubMed ID: 20042712
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  • 11. Curcumin does not stimulate cAMP-mediated chloride transport in cystic fibrosis airway epithelial cells.
    Dragomir A, Björstad J, Hjelte L, Roomans GM.
    Biochem Biophys Res Commun; 2004 Sep 17; 322(2):447-51. PubMed ID: 15325250
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  • 20. Role of tyrosine phosphorylation in the muscarinic activation of the cystic fibrosis transmembrane conductance regulator (CFTR).
    Billet A, Luo Y, Balghi H, Hanrahan JW.
    J Biol Chem; 2013 Jul 26; 288(30):21815-23. PubMed ID: 23760269
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