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Journal Abstract Search

674 related items for PubMed ID: 17339840

  • 1. 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; 150(8):1055-65. PubMed ID: 17339840
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  • 2. Activation of intestinal Cl- secretion by lubiprostone requires the cystic fibrosis transmembrane conductance regulator.
    Bijvelds MJ, Bot AG, Escher JC, De Jonge HR.
    Gastroenterology; 2009 Sep; 137(3):976-85. PubMed ID: 19454284
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  • 4. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.
    Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C.
    Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100
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  • 5. TGFbeta down-regulation of the CFTR: a means to limit epithelial chloride secretion.
    Howe KL, Wang A, Hunter MM, Stanton BA, McKay DM.
    Exp Cell Res; 2004 Aug 15; 298(2):473-84. PubMed ID: 15265695
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  • 6. Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.
    Antigny F, Norez C, Dannhoffer L, Bertrand J, Raveau D, Corbi P, Jayle C, Becq F, Vandebrouck C.
    Am J Respir Cell Mol Biol; 2011 Jan 15; 44(1):83-90. PubMed ID: 20203293
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  • 7. CFTR-mediated chloride permeability is regulated by type III phosphodiesterases in airway epithelial cells.
    Kelley TJ, al-Nakkash L, Drumm ML.
    Am J Respir Cell Mol Biol; 1995 Dec 15; 13(6):657-64. PubMed ID: 7576703
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  • 11. Bioelectric characterization of epithelia from neonatal CFTR knockout ferrets.
    Fisher JT, Tyler SR, Zhang Y, Lee BJ, Liu X, Sun X, Sui H, Liang B, Luo M, Xie W, Yi Y, Zhou W, Song Y, Keiser N, Wang K, de Jonge HR, Engelhardt JF.
    Am J Respir Cell Mol Biol; 2013 Nov 15; 49(5):837-44. PubMed ID: 23782101
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  • 15. Purinergic signaling underlies CFTR control of human airway epithelial cell volume.
    Braunstein GM, Zsembery A, Tucker TA, Schwiebert EM.
    J Cyst Fibros; 2004 Jun 15; 3(2):99-117. PubMed ID: 15463893
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  • 16. Epithelial sodium channel inhibition in primary human bronchial epithelia by transfected siRNA.
    Caci E, Melani R, Pedemonte N, Yueksekdag G, Ravazzolo R, Rosenecker J, Galietta LJ, Zegarra-Moran O.
    Am J Respir Cell Mol Biol; 2009 Feb 15; 40(2):211-6. PubMed ID: 18723440
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  • 17. Cordyceps militaris extract stimulates Cl(-) secretion across human bronchial epithelia by both Ca(2+)(-) and cAMP-dependent pathways.
    Fung JC, Yue GG, Fung KP, Ma X, Yao XQ, Ko WH.
    J Ethnopharmacol; 2011 Oct 31; 138(1):201-11. PubMed ID: 21939749
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  • 18. CFTR in Calu-3 human airway cells: channel properties and role in cAMP-activated Cl- conductance.
    Haws C, Finkbeiner WE, Widdicombe JH, Wine JJ.
    Am J Physiol; 1994 May 31; 266(5 Pt 1):L502-12. PubMed ID: 7515579
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  • 19. Dual activation of CFTR and CLCN2 by lubiprostone in murine nasal epithelia.
    Schiffhauer ES, Vij N, Kovbasnjuk O, Kang PW, Walker D, Lee S, Zeitlin PL.
    Am J Physiol Lung Cell Mol Physiol; 2013 Mar 01; 304(5):L324-31. PubMed ID: 23316067
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