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154 related items for PubMed ID: 9374850

  • 1. A functional CFTR-NBF1 is required for ROMK2-CFTR interaction.
    McNicholas CM, Nason MW, Guggino WB, Schwiebert EM, Hebert SC, Giebisch G, Egan ME.
    Am J Physiol; 1997 Nov; 273(5):F843-8. PubMed ID: 9374850
    [Abstract] [Full Text] [Related]

  • 2. Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator.
    McNicholas CM, Guggino WB, Schwiebert EM, Hebert SC, Giebisch G, Egan ME.
    Proc Natl Acad Sci U S A; 1996 Jul 23; 93(15):8083-8. PubMed ID: 8755607
    [Abstract] [Full Text] [Related]

  • 3. Identification of the cystic fibrosis transmembrane conductance regulator domains that are important for interactions with ROMK2.
    Cahill P, Nason MW, Ambrose C, Yao TY, Thomas P, Egan ME.
    J Biol Chem; 2000 Jun 02; 275(22):16697-701. PubMed ID: 10748197
    [Abstract] [Full Text] [Related]

  • 4. Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte.
    Tanemoto M, Vanoye CG, Dong K, Welch R, Abe T, Hebert SC, Xu JZ.
    Am J Physiol Renal Physiol; 2000 Apr 02; 278(4):F659-66. PubMed ID: 10751228
    [Abstract] [Full Text] [Related]

  • 5. Cystic fibrosis transmembrane conductance regulator mediates sulphonylurea block of the inwardly rectifying K+ channel Kir6.1.
    Ishida-Takahashi A, Otani H, Takahashi C, Washizuka T, Tsuji K, Noda M, Horie M, Sasayama S.
    J Physiol; 1998 Apr 01; 508 ( Pt 1)(Pt 1):23-30. PubMed ID: 9490811
    [Abstract] [Full Text] [Related]

  • 6. Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator.
    Schwiebert EM, Morales MM, Devidas S, Egan ME, Guggino WB.
    Proc Natl Acad Sci U S A; 1998 Mar 03; 95(5):2674-9. PubMed ID: 9482946
    [Abstract] [Full Text] [Related]

  • 7. PKA site mutations of ROMK2 channels shift the pH dependence to more alkaline values.
    Leipziger J, MacGregor GG, Cooper GJ, Xu J, Hebert SC, Giebisch G.
    Am J Physiol Renal Physiol; 2000 Nov 03; 279(5):F919-26. PubMed ID: 11053053
    [Abstract] [Full Text] [Related]

  • 8. Functional roles of nonconserved structural segments in CFTR's NH2-terminal nucleotide binding domain.
    Csanády L, Chan KW, Nairn AC, Gadsby DC.
    J Gen Physiol; 2005 Jan 03; 125(1):43-55. PubMed ID: 15596536
    [Abstract] [Full Text] [Related]

  • 9. Changes in voltage activation, Cs+ sensitivity, and ion permeability in H5 mutants of the plant K+ channel KAT1.
    Becker D, Dreyer I, Hoth S, Reid JD, Busch H, Lehnen M, Palme K, Hedrich R.
    Proc Natl Acad Sci U S A; 1996 Jul 23; 93(15):8123-8. PubMed ID: 8755614
    [Abstract] [Full Text] [Related]

  • 10. The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.
    Schreiber R, Hopf A, Mall M, Greger R, Kunzelmann K.
    Proc Natl Acad Sci U S A; 1999 Apr 27; 96(9):5310-5. PubMed ID: 10220462
    [Abstract] [Full Text] [Related]

  • 11. Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents.
    Sheppard DN, Welsh MJ.
    J Gen Physiol; 1992 Oct 27; 100(4):573-91. PubMed ID: 1281220
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. An amino acid triplet in the NH2 terminus of rat ROMK1 determines interaction with SUR2B.
    Dong K, Xu J, Vanoye CG, Welch R, MacGregor GG, Giebisch G, Hebert SC.
    J Biol Chem; 2001 Nov 23; 276(47):44347-53. PubMed ID: 11567030
    [Abstract] [Full Text] [Related]

  • 14. Regulation of recombinant cardiac cystic fibrosis transmembrane conductance regulator chloride channels by protein kinase C.
    Yamazaki J, Britton F, Collier ML, Horowitz B, Hume JR.
    Biophys J; 1999 Apr 23; 76(4):1972-87. PubMed ID: 10096895
    [Abstract] [Full Text] [Related]

  • 15. Phosphorylation of the ATP-sensitive, inwardly rectifying K+ channel, ROMK, by cyclic AMP-dependent protein kinase.
    Xu ZC, Yang Y, Hebert SC.
    J Biol Chem; 1996 Apr 19; 271(16):9313-9. PubMed ID: 8621594
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Expression of CFTR controls cAMP-dependent activation of epithelial K+ currents.
    Loussouarn G, Demolombe S, Mohammad-Panah R, Escande D, Baró I.
    Am J Physiol; 1996 Nov 27; 271(5 Pt 1):C1565-73. PubMed ID: 8944640
    [Abstract] [Full Text] [Related]

  • 18. Cystic fibrosis transmembrane conductance regulator-dependent up-regulation of Kir1.1 (ROMK) renal K+ channels by the epithelial sodium channel.
    Konstas AA, Koch JP, Tucker SJ, Korbmacher C.
    J Biol Chem; 2002 Jul 12; 277(28):25377-84. PubMed ID: 11994290
    [Abstract] [Full Text] [Related]

  • 19. Intrinsic sensitivity of Kir1.1 (ROMK) to glibenclamide in the absence of SUR2B. Implications for the identity of the renal ATP-regulated secretory K+ channel.
    Konstas AA, Dabrowski M, Korbmacher C, Tucker SJ.
    J Biol Chem; 2002 Jun 14; 277(24):21346-51. PubMed ID: 11927600
    [Abstract] [Full Text] [Related]

  • 20. Inactivating properties of recombinant ROMK2 channels expressed in mammalian cells.
    Riochet DF, Mohammad-Panah R, Hebert SC, MacGregor GG, Baró I, Guihard G, Escande D.
    Biochem Biophys Res Commun; 2001 Aug 17; 286(2):376-80. PubMed ID: 11500048
    [Abstract] [Full Text] [Related]

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