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75 related items for PubMed ID: 10501833

  • 21. Genistein and tyrphostin 47 stimulate CFTR-mediated Cl- secretion in T84 cell monolayers.
    Sears CL, Firoozmand F, Mellander A, Chambers FG, Eromar IG, Bot AG, Scholte B, De Jonge HR, Donowitz M.
    Am J Physiol; 1995 Dec; 269(6 Pt 1):G874-82. PubMed ID: 8572219
    [Abstract] [Full Text] [Related]

  • 22. Extracellular UTP stimulates electrogenic bicarbonate secretion across CFTR knockout gallbladder epithelium.
    Clarke LL, Harline MC, Gawenis LR, Walker NM, Turner JT, Weisman GA.
    Am J Physiol Gastrointest Liver Physiol; 2000 Jul; 279(1):G132-8. PubMed ID: 10898755
    [Abstract] [Full Text] [Related]

  • 23. cAMP and genistein stimulate HCO3- conductance through CFTR in human airway epithelia.
    Illek B, Yankaskas JR, Machen TE.
    Am J Physiol; 1997 Apr; 272(4 Pt 1):L752-61. PubMed ID: 9142951
    [Abstract] [Full Text] [Related]

  • 24. Effect of VX-770 (ivacaftor) and OAG on Ca2+ influx and CFTR activity in G551D and F508del-CFTR expressing cells.
    Vachel L, Norez C, Becq F, Vandebrouck C.
    J Cyst Fibros; 2013 Dec; 12(6):584-91. PubMed ID: 23757361
    [Abstract] [Full Text] [Related]

  • 25. Regulation of murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in Chinese hamster ovary cells.
    Lansdell KA, Kidd JF, Delaney SJ, Wainwright BJ, Sheppard DN.
    J Physiol; 1998 Nov 01; 512 ( Pt 3)(Pt 3):751-64. PubMed ID: 9769419
    [Abstract] [Full Text] [Related]

  • 26. Cystic fibrosis transmembrane conductance regulator (CFTR) confers glibenclamide sensitivity to outwardly rectifying chloride channel (ORCC) in Hi-5 insect cells.
    Julien M, Verrier B, Cerutti M, Chappe V, Gola M, Devauchelle G, Becq F.
    J Membr Biol; 1999 Apr 01; 168(3):229-39. PubMed ID: 10191357
    [Abstract] [Full Text] [Related]

  • 27. Interaction between calcium-activated chloride channels and the cystic fibrosis transmembrane conductance regulator.
    Wei L, Vankeerberghen A, Cuppens H, Eggermont J, Cassiman JJ, Droogmans G, Nilius B.
    Pflugers Arch; 1999 Oct 01; 438(5):635-41. PubMed ID: 10555560
    [Abstract] [Full Text] [Related]

  • 28. Differential regulation of single CFTR channels by PP2C, PP2A, and other phosphatases.
    Luo J, Pato MD, Riordan JR, Hanrahan JW.
    Am J Physiol; 1998 May 01; 274(5):C1397-410. PubMed ID: 9612228
    [Abstract] [Full Text] [Related]

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  • 31. Polarized signaling via purinoceptors in normal and cystic fibrosis airway epithelia.
    Paradiso AM, Ribeiro CM, Boucher RC.
    J Gen Physiol; 2001 Jan 01; 117(1):53-67. PubMed ID: 11134231
    [Abstract] [Full Text] [Related]

  • 32. On the mechanism of gating defects caused by the R117H mutation in cystic fibrosis transmembrane conductance regulator.
    Yu YC, Sohma Y, Hwang TC.
    J Physiol; 2016 Jun 15; 594(12):3227-44. PubMed ID: 26846474
    [Abstract] [Full Text] [Related]

  • 33. P2Y purinergic receptor regulation of CFTR chloride channels in mouse cardiac myocytes.
    Yamamoto-Mizuma S, Wang GX, Hume JR.
    J Physiol; 2004 May 01; 556(Pt 3):727-37. PubMed ID: 14978203
    [Abstract] [Full Text] [Related]

  • 34. General anesthetic octanol and related compounds activate wild-type and delF508 cystic fibrosis chloride channels.
    Marcet B, Becq F, Norez C, Delmas P, Verrier B.
    Br J Pharmacol; 2004 Mar 01; 141(6):905-14. PubMed ID: 14967738
    [Abstract] [Full Text] [Related]

  • 35. Multiple intracellular pathways for regulation of chloride secretion in cultured pig tracheal submucosal gland cells.
    Zhang AL, Roomans GM.
    Eur Respir J; 1999 Mar 01; 13(3):571-6. PubMed ID: 10232428
    [Abstract] [Full Text] [Related]

  • 36. 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 01; 1812(11):1385-92. PubMed ID: 21907281
    [Abstract] [Full Text] [Related]

  • 37. Activation of an adenosine 3',5'-cyclic monophosphate-dependent Cl- conductance in response to neurohormonal stimuli in mouse endometrial epithelial cells: the role of cystic fibrosis transmembrane conductance regulator.
    Chan LN, Chung YW, Leung PS, Liu CQ, Chan HC.
    Biol Reprod; 1999 Feb 01; 60(2):374-80. PubMed ID: 9916004
    [Abstract] [Full Text] [Related]

  • 38. Ursodeoxycholic acid stimulates cholangiocyte fluid secretion in mice via CFTR-dependent ATP secretion.
    Fiorotto R, Spirlì C, Fabris L, Cadamuro M, Okolicsanyi L, Strazzabosco M.
    Gastroenterology; 2007 Nov 01; 133(5):1603-13. PubMed ID: 17983806
    [Abstract] [Full Text] [Related]

  • 39. Cell-based assay for high-throughput quantitative screening of CFTR chloride transport agonists.
    Galietta LV, Jayaraman S, Verkman AS.
    Am J Physiol Cell Physiol; 2001 Nov 01; 281(5):C1734-42. PubMed ID: 11600438
    [Abstract] [Full Text] [Related]

  • 40. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
    Johnson LG, Boyles SE, Wilson J, Boucher RC.
    J Clin Invest; 1995 Mar 01; 95(3):1377-82. PubMed ID: 7533790
    [Abstract] [Full Text] [Related]

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