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Journal Abstract Search

243 related items for PubMed ID: 16470247

  • 1. CFTR is required for PKA-regulated ATP sensitivity of Kir1.1 potassium channels in mouse kidney.
    Lu M, Leng Q, Egan ME, Caplan MJ, Boulpaep EL, Giebisch GH, Hebert SC.
    J Clin Invest; 2006 Mar; 116(3):797-807. PubMed ID: 16470247
    [Abstract] [Full Text] [Related]

  • 2. Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct.
    Lu M, Dong K, Egan ME, Giebisch GH, Boulpaep EL, Hebert SC.
    Proc Natl Acad Sci U S A; 2010 Mar 30; 107(13):6082-7. PubMed ID: 20231442
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  • 3. Protein-protein interactions among ion channels regulate ion transport in the kidney.
    Boulpaep E.
    Bull Mem Acad R Med Belg; 2009 Mar 30; 164(3-4):133-41; discussion 141-2. PubMed ID: 20120088
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  • 7. Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.
    Stanton BA.
    Wien Klin Wochenschr; 1997 Jun 27; 109(12-13):457-64. PubMed ID: 9261986
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  • 8. Potentiation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl- currents by the chemical solvent tetrahydrofuran.
    Hughes LK, Ju M, Sheppard DN.
    Mol Membr Biol; 2008 Sep 27; 25(6-7):528-38. PubMed ID: 18989824
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  • 9. Novel subunit composition of a renal epithelial KATP channel.
    Ruknudin A, Schulze DH, Sullivan SK, Lederer WJ, Welling PA.
    J Biol Chem; 1998 Jun 05; 273(23):14165-71. PubMed ID: 9603917
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  • 12. WNK3, a kinase related to genes mutated in hereditary hypertension with hyperkalaemia, regulates the K+ channel ROMK1 (Kir1.1).
    Leng Q, Kahle KT, Rinehart J, MacGregor GG, Wilson FH, Canessa CM, Lifton RP, Hebert SC.
    J Physiol; 2006 Mar 01; 571(Pt 2):275-86. PubMed ID: 16357011
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  • 13. ENaC activity requires CFTR channel function independently of phosphorylation in sweat duct.
    Reddy MM, Quinton PM.
    J Membr Biol; 2005 Sep 01; 207(1):23-33. PubMed ID: 16463140
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  • 14. Simple binding of protein kinase A prior to phosphorylation allows CFTR anion channels to be opened by nucleotides.
    Mihályi C, Iordanov I, Töröcsik B, Csanády L.
    Proc Natl Acad Sci U S A; 2020 Sep 01; 117(35):21740-21746. PubMed ID: 32817533
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  • 15. Defective formation of PKA/CnA-dependent annexin 2-S100A10/CFTR complex in DeltaF508 cystic fibrosis cells.
    Borthwick LA, Riemen C, Goddard C, Colledge WH, Mehta A, Gerke V, Muimo R.
    Cell Signal; 2008 Jun 01; 20(6):1073-83. PubMed ID: 18346874
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  • 16. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
    Reddy MM, Quinton PM.
    JOP; 2001 Jul 01; 2(4 Suppl):212-8. PubMed ID: 11875262
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  • 17. 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
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  • 18. 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 01; 76(4):1972-87. PubMed ID: 10096895
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  • 19. Glibenclamide stimulates fluid secretion in rodent cholangiocytes through a cystic fibrosis transmembrane conductance regulator-independent mechanism.
    Spirlì C, Fiorotto R, Song L, Santos-Sacchi J, Okolicsanyi L, Masier S, Rocchi L, Vairetti MP, De Bernard M, Melero S, Pozzan T, Strazzabosco M.
    Gastroenterology; 2005 Jul 01; 129(1):220-33. PubMed ID: 16012949
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  • 20. The ROMK-cystic fibrosis transmembrane conductance regulator connection: new insights into the relationship between ROMK and cystic fibrosis transmembrane conductance regulator channels.
    Ho K.
    Curr Opin Nephrol Hypertens; 1998 Jan 01; 7(1):49-58. PubMed ID: 9442363
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