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182 related items for PubMed ID: 1719763

  • 1. Cystic fibrosis, the CFTR, and rectifying Cl- channels.
    Wine JJ, Brayden DJ, Hagiwara G, Krouse ME, Law TC, Müller UJ, Solc CK, Ward CL, Widdicombe JH, Xia Y.
    Adv Exp Med Biol; 1991; 290():253-69; discussion 269-72. PubMed ID: 1719763
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  • 2. CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship.
    Gabriel SE, Clarke LL, Boucher RC, Stutts MJ.
    Nature; 1993 May 20; 363(6426):263-8. PubMed ID: 7683773
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  • 6. Outwardly rectifying chloride channels and CF: a divorce and remarriage.
    Guggino WB.
    J Bioenerg Biomembr; 1993 Feb 20; 25(1):27-35. PubMed ID: 7680029
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  • 9. Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR.
    Egan M, Flotte T, Afione S, Solow R, Zeitlin PL, Carter BJ, Guggino WB.
    Nature; 1992 Aug 13; 358(6387):581-4. PubMed ID: 1380129
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  • 10. Human lymphocytes transcribe the cystic fibrosis transmembrane conductance regulator gene and exhibit CF-defective cAMP-regulated chloride current.
    McDonald TV, Nghiem PT, Gardner P, Martens CL.
    J Biol Chem; 1992 Feb 15; 267(5):3242-8. PubMed ID: 1371114
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  • 17. 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 15; 266(5 Pt 1):L502-12. PubMed ID: 7515579
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  • 19. Disruption of monolayer integrity enables activation of a cystic fibrosis "bypass" channel in human airway epithelia.
    Xia Y, Haws CM, Wine JJ.
    Nat Med; 1997 Jul 15; 3(7):802-5. PubMed ID: 9212112
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