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 *

270 related articles for article (PubMed ID: 25892339)

  • 1. Interactions between permeant and blocking anions inside the CFTR chloride channel pore.
    Linsdell P
    Biochim Biophys Acta; 2015 Jul; 1848(7):1573-90. PubMed ID: 25892339
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interactions between impermeant blocking ions in the cystic fibrosis transmembrane conductance regulator chloride channel pore: evidence for anion-induced conformational changes.
    Ge N; Linsdell P
    J Membr Biol; 2006 Mar; 210(1):31-42. PubMed ID: 16794779
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. State-dependent blocker interactions with the CFTR chloride channel: implications for gating the pore.
    Linsdell P
    Pflugers Arch; 2014 Dec; 466(12):2243-55. PubMed ID: 24671572
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Anion conductance selectivity mechanism of the CFTR chloride channel.
    Linsdell P
    Biochim Biophys Acta; 2016 Apr; 1858(4):740-7. PubMed ID: 26779604
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a second blocker binding site at the cytoplasmic mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    St Aubin CN; Zhou JJ; Linsdell P
    Mol Pharmacol; 2007 May; 71(5):1360-8. PubMed ID: 17293558
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Monovalent: Divalent Anion Selectivity in the CFTR Channel Pore.
    Linsdell P
    Cell Biochem Biophys; 2021 Dec; 79(4):863-871. PubMed ID: 34031860
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore.
    Gong X; Linsdell P
    J Gen Physiol; 2003 Dec; 122(6):673-87. PubMed ID: 14610019
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trivalent anions as probes of the CFTR channel pore.
    Linsdell P
    Gen Physiol Biophys; 2024 May; 43(3):197-207. PubMed ID: 38774920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Location of a permeant anion binding site in the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Rubaiy HN; Linsdell P
    J Physiol Sci; 2015 May; 65(3):233-41. PubMed ID: 25673337
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular determinants and role of an anion binding site in the external mouth of the CFTR chloride channel pore.
    Gong X; Linsdell P
    J Physiol; 2003 Jun; 549(Pt 2):387-97. PubMed ID: 12679372
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Coupled movement of permeant and blocking ions in the CFTR chloride channel pore.
    Gong X; Linsdell P
    J Physiol; 2003 Jun; 549(Pt 2):375-85. PubMed ID: 12679371
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional organization of cytoplasmic portals controlling access to the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel pore.
    Li MS; Cowley EA; El Hiani Y; Linsdell P
    J Biol Chem; 2018 Apr; 293(15):5649-5658. PubMed ID: 29475947
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Location of a common inhibitor binding site in the cytoplasmic vestibule of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Linsdell P
    J Biol Chem; 2005 Mar; 280(10):8945-50. PubMed ID: 15634668
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maximization of the rate of chloride conduction in the CFTR channel pore by ion-ion interactions.
    Gong X; Linsdell P
    Arch Biochem Biophys; 2004 Jun; 426(1):78-82. PubMed ID: 15130785
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Direct and indirect effects of mutations at the outer mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Zhou JJ; Fatehi M; Linsdell P
    J Membr Biol; 2007 Apr; 216(2-3):129-42. PubMed ID: 17673962
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Linsdell P
    J Physiol; 2001 Feb; 531(Pt 1):51-66. PubMed ID: 11179391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore.
    Zhou JJ; Li MS; Qi J; Linsdell P
    J Gen Physiol; 2010 Mar; 135(3):229-45. PubMed ID: 20142516
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.