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 *

192 related articles for article (PubMed ID: 25867140)

  • 21. G551D mutation impairs PKA-dependent activation of CFTR channel that can be restored by novel GOF mutations.
    Wang W; Fu L; Liu Z; Wen H; Rab A; Hong JS; Kirk KL; Rowe SM
    Am J Physiol Lung Cell Mol Physiol; 2020 Nov; 319(5):L770-L785. PubMed ID: 32877225
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Functional stability of CFTR depends on tight binding of ATP at its degenerate ATP-binding site.
    Yeh HI; Yu YC; Kuo PL; Tsai CK; Huang HT; Hwang TC
    J Physiol; 2021 Oct; 599(20):4625-4642. PubMed ID: 34411298
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The glycine residues G551 and G1349 within the ATP-binding cassette signature motifs play critical roles in the activation and inhibition of cystic fibrosis transmembrane conductance regulator channels by phloxine B.
    Melin P; Norez C; Callebaut I; Becq F
    J Membr Biol; 2005 Dec; 208(3):203-12. PubMed ID: 16604470
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state.
    Xie J; Drumm ML; Ma J; Davis PB
    J Biol Chem; 1995 Nov; 270(47):28084-91. PubMed ID: 7499295
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability.
    Meng X; Clews J; Kargas V; Wang X; Ford RC
    Cell Mol Life Sci; 2017 Jan; 74(1):23-38. PubMed ID: 27734094
    [TBL] [Abstract][Full Text] [Related]  

  • 26. How Phosphorylation and ATPase Activity Regulate Anion Flux though the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR).
    Zwick M; Esposito C; Hellstern M; Seelig A
    J Biol Chem; 2016 Jul; 291(28):14483-98. PubMed ID: 27226582
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An electrostatic interaction at the tetrahelix bundle promotes phosphorylation-dependent cystic fibrosis transmembrane conductance regulator (CFTR) channel opening.
    Wang W; Roessler BC; Kirk KL
    J Biol Chem; 2014 Oct; 289(44):30364-30378. PubMed ID: 25190805
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Direct sensing of intracellular pH by the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel.
    Chen JH; Cai Z; Sheppard DN
    J Biol Chem; 2009 Dec; 284(51):35495-506. PubMed ID: 19837660
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Non-native Conformers of Cystic Fibrosis Transmembrane Conductance Regulator NBD1 Are Recognized by Hsp27 and Conjugated to SUMO-2 for Degradation.
    Gong X; Ahner A; Roldan A; Lukacs GL; Thibodeau PH; Frizzell RA
    J Biol Chem; 2016 Jan; 291(4):2004-2017. PubMed ID: 26627832
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The gating of the CFTR channel.
    Moran O
    Cell Mol Life Sci; 2017 Jan; 74(1):85-92. PubMed ID: 27696113
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Structural stability of purified human CFTR is systematically improved by mutations in nucleotide binding domain 1.
    Yang Z; Hildebrandt E; Jiang F; Aleksandrov AA; Khazanov N; Zhou Q; An J; Mezzell AT; Xavier BM; Ding H; Riordan JR; Senderowitz H; Kappes JC; Brouillette CG; Urbatsch IL
    Biochim Biophys Acta Biomembr; 2018 May; 1860(5):1193-1204. PubMed ID: 29425673
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Insights into the mechanisms underlying CFTR channel activity, the molecular basis for cystic fibrosis and strategies for therapy.
    Kim Chiaw P; Eckford PD; Bear CE
    Essays Biochem; 2011 Sep; 50(1):233-48. PubMed ID: 21967060
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Fluorescence assay for simultaneous quantification of CFTR ion-channel function and plasma membrane proximity.
    Prins S; Langron E; Hastings C; Hill EJ; Stefan AC; Griffin LD; Vergani P
    J Biol Chem; 2020 Dec; 295(49):16529-16544. PubMed ID: 32934006
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels.
    Mickle JE; Milewski MI; Macek M; Cutting GR
    Am J Hum Genet; 2000 May; 66(5):1485-95. PubMed ID: 10762539
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.
    Li C; Naren AP
    Pharmacol Ther; 2005 Nov; 108(2):208-23. PubMed ID: 15936089
    [TBL] [Abstract][Full Text] [Related]  

  • 36. CFTR potentiators partially restore channel function to A561E-CFTR, a cystic fibrosis mutant with a similar mechanism of dysfunction as F508del-CFTR.
    Wang Y; Liu J; Loizidou A; Bugeja LA; Warner R; Hawley BR; Cai Z; Toye AM; Sheppard DN; Li H
    Br J Pharmacol; 2014 Oct; 171(19):4490-503. PubMed ID: 24902474
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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; 76(4):1972-87. PubMed ID: 10096895
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 107(13):6082-7. PubMed ID: 20231442
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Differential function of the two nucleotide binding domains on cystic fibrosis transmembrane conductance regulator.
    Nagel G
    Biochim Biophys Acta; 1999 Dec; 1461(2):263-74. PubMed ID: 10581360
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Channel Gating Regulation by the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) First Cytosolic Loop.
    Ehrhardt A; Chung WJ; Pyle LC; Wang W; Nowotarski K; Mulvihill CM; Ramjeesingh M; Hong J; Velu SE; Lewis HA; Atwell S; Aller S; Bear CE; Lukacs GL; Kirk KL; Sorscher EJ
    J Biol Chem; 2016 Jan; 291(4):1854-1865. PubMed ID: 26627831
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.