These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 9922376)

  • 21. Structure and function of the CFTR chloride channel.
    Sheppard DN; Welsh MJ
    Physiol Rev; 1999 Jan; 79(1 Suppl):S23-45. PubMed ID: 9922375
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cystic fibrosis transmembrane conductance regulator: using differential reactivity toward channel-permeant and channel-impermeant thiol-reactive probes to test a molecular model for the pore.
    Alexander C; Ivetac A; Liu X; Norimatsu Y; Serrano JR; Landstrom A; Sansom M; Dawson DC
    Biochemistry; 2009 Oct; 48(42):10078-88. PubMed ID: 19754156
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evidence that extracellular anions interact with a site outside the CFTR chloride channel pore to modify channel properties.
    Zhou JJ; Linsdell P
    Can J Physiol Pharmacol; 2009 May; 87(5):387-95. PubMed ID: 19448737
    [TBL] [Abstract][Full Text] [Related]  

  • 24. CFTR structure and cystic fibrosis.
    Cant N; Pollock N; Ford RC
    Int J Biochem Cell Biol; 2014 Jul; 52():15-25. PubMed ID: 24534272
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Linsdell P
    Exp Physiol; 2006 Jan; 91(1):123-9. PubMed ID: 16157656
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Atomic Structure of the Cystic Fibrosis Transmembrane Conductance Regulator.
    Zhang Z; Chen J
    Cell; 2016 Dec; 167(6):1586-1597.e9. PubMed ID: 27912062
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Structural Changes Fundamental to Gating of the Cystic Fibrosis Transmembrane Conductance Regulator Anion Channel Pore.
    Linsdell P
    Adv Exp Med Biol; 2017; 925():13-32. PubMed ID: 27311317
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells.
    Reddy MM; Quinton PM
    Nature; 2003 Jun; 423(6941):756-60. PubMed ID: 12802335
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Intracellular CFTR: localization and function.
    Bradbury NA
    Physiol Rev; 1999 Jan; 79(1 Suppl):S175-91. PubMed ID: 9922381
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular modelling approaches for cystic fibrosis transmembrane conductance regulator studies.
    Odolczyk N; Zielenkiewicz P
    Int J Biochem Cell Biol; 2014 Jul; 52():39-46. PubMed ID: 24735712
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Flickery block of single CFTR chloride channels by intracellular anions and osmolytes.
    Linsdell P; Hanrahan JW
    Am J Physiol; 1996 Aug; 271(2 Pt 1):C628-34. PubMed ID: 8770004
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biochemical implications of sequence comparisons of the cystic fibrosis transmembrane conductance regulator.
    Tan AL; Ong SA; Venkatesh B
    Arch Biochem Biophys; 2002 May; 401(2):215-22. PubMed ID: 12054472
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Small molecule anionophores promote transmembrane anion permeation matching CFTR activity.
    Hernando E; Capurro V; Cossu C; Fiore M; García-Valverde M; Soto-Cerrato V; Pérez-Tomás R; Moran O; Zegarra-Moran O; Quesada R
    Sci Rep; 2018 Feb; 8(1):2608. PubMed ID: 29422673
    [TBL] [Abstract][Full Text] [Related]  

  • 34. On the origin of asymmetric interactions between permeant anions and the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Fatehi M; St Aubin CN; Linsdell P
    Biophys J; 2007 Feb; 92(4):1241-53. PubMed ID: 17142267
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cystic fibrosis transmembrane conductance regulator: a molecular model defines the architecture of the anion conduction path and locates a "bottleneck" in the pore.
    Norimatsu Y; Ivetac A; Alexander C; Kirkham J; O'Donnell N; Dawson DC; Sansom MS
    Biochemistry; 2012 Mar; 51(11):2199-212. PubMed ID: 22352759
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): physiological and pathophysiological relevance.
    El Khouri E; Touré A
    Int J Biochem Cell Biol; 2014 Jul; 52():58-67. PubMed ID: 24530837
    [TBL] [Abstract][Full Text] [Related]  

  • 37. CFTR-Mediated anion conductance regulates Na(+)-K(+)-pump activity in Calu-3 human airway cells.
    Ito Y; Mizuno Y; Aoyama M; Kume H; Yamaki K
    Biochem Biophys Res Commun; 2000 Jul; 274(1):230-5. PubMed ID: 10903923
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Topogenesis of cystic fibrosis transmembrane conductance regulator (CFTR): regulation by the amino terminal transmembrane sequences.
    Chen M; Zhang JT
    Biochemistry; 1999 Apr; 38(17):5471-7. PubMed ID: 10220334
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cystic fibrosis transmembrane conductance regulator: the first nucleotide binding fold targets the membrane with retention of its ATP binding function.
    Ko YH; Delannoy M; Pedersen PL
    Biochemistry; 1997 Apr; 36(16):5053-64. PubMed ID: 9125527
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Positive charges at the intracellular mouth of the pore regulate anion conduction in the CFTR chloride channel.
    Aubin CN; Linsdell P
    J Gen Physiol; 2006 Nov; 128(5):535-45. PubMed ID: 17043152
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.