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 *

126 related articles for article (PubMed ID: 15504728)

  • 21. Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore.
    El Hiani Y; Linsdell P
    J Biol Chem; 2015 Jun; 290(25):15855-15865. PubMed ID: 25944907
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules.
    Zerhusen B; Zhao J; Xie J; Davis PB; Ma J
    J Biol Chem; 1999 Mar; 274(12):7627-30. PubMed ID: 10075649
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. CFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction.
    Smith SS; Liu X; Zhang ZR; Sun F; Kriewall TE; McCarty NA; Dawson DC
    J Gen Physiol; 2001 Oct; 118(4):407-31. PubMed ID: 11585852
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Altering intracellular pH reveals the kinetic basis of intraburst gating in the CFTR Cl
    Chen JH; Xu W; Sheppard DN
    J Physiol; 2017 Feb; 595(4):1059-1076. PubMed ID: 27779763
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Role of the juxtamembrane region of cytoplasmic loop 3 in the gating and conductance of the cystic fibrosis transmembrane conductance regulator chloride channel.
    El Hiani Y; Linsdell P
    Biochemistry; 2012 May; 51(19):3971-81. PubMed ID: 22545782
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Functional differences in pore properties between wild-type and cysteine-less forms of the CFTR chloride channel.
    Holstead RG; Li MS; Linsdell P
    J Membr Biol; 2011 Oct; 243(1-3):15-23. PubMed ID: 21796426
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel residues lining the CFTR chloride channel pore identified by functional modification of introduced cysteines.
    Fatehi M; Linsdell P
    J Membr Biol; 2009 Apr; 228(3):151-64. PubMed ID: 19381710
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Emerging issues of connexin channels: biophysics fills the gap.
    Harris AL
    Q Rev Biophys; 2001 Aug; 34(3):325-472. PubMed ID: 11838236
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. The Fifth Transmembrane Segment of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Its Anion Permeation Pathway.
    Zhang J; Hwang TC
    Biochemistry; 2015 Jun; 54(24):3839-50. PubMed ID: 26024338
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. The pore architecture of the cystic fibrosis transmembrane conductance regulator channel revealed by co-mutation in pore-forming transmembrane regions.
    Qian F; Liu L; Liu Z; Lu C
    Physiol Res; 2016 Jul; 65(3):505-15. PubMed ID: 27070741
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Two salt bridges differentially contribute to the maintenance of cystic fibrosis transmembrane conductance regulator (CFTR) channel function.
    Cui G; Freeman CS; Knotts T; Prince CZ; Kuang C; McCarty NA
    J Biol Chem; 2013 Jul; 288(28):20758-67. PubMed ID: 23709221
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Human epithelial cystic fibrosis transmembrane conductance regulator without exon 5 maintains partial chloride channel function in intracellular membranes.
    Xie J; Drumm ML; Zhao J; Ma J; Davis PB
    Biophys J; 1996 Dec; 71(6):3148-56. PubMed ID: 8968585
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Conformational changes in a pore-lining helix coupled to cystic fibrosis transmembrane conductance regulator channel gating.
    Beck EJ; Yang Y; Yaemsiri S; Raghuram V
    J Biol Chem; 2008 Feb; 283(8):4957-66. PubMed ID: 18056267
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia.
    Dong Q; Ernst SE; Ostedgaard LS; Shah VS; Ver Heul AR; Welsh MJ; Randak CO
    J Biol Chem; 2015 May; 290(22):14140-53. PubMed ID: 25887396
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Severed molecules functionally define the boundaries of the cystic fibrosis transmembrane conductance regulator's NH(2)-terminal nucleotide binding domain.
    Chan KW; Csanády L; Seto-Young D; Nairn AC; Gadsby DC
    J Gen Physiol; 2000 Aug; 116(2):163-80. PubMed ID: 10919864
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.