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 *

109 related articles for article (PubMed ID: 20080601)

  • 21. Stable ATP binding mediated by a partial NBD dimer of the CFTR chloride channel.
    Tsai MF; Li M; Hwang TC
    J Gen Physiol; 2010 May; 135(5):399-414. PubMed ID: 20421370
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Gating of the CFTR Cl- channel by ATP-driven nucleotide-binding domain dimerisation.
    Hwang TC; Sheppard DN
    J Physiol; 2009 May; 587(Pt 10):2151-61. PubMed ID: 19332488
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [ATP hydrolysis-driven gating of an ABC transporter CFTR channel: from stills to movies].
    Sohma Y; Yamashita H
    Nihon Yakurigaku Zasshi; 2013 May; 141(5):230-4. PubMed ID: 23665551
    [No Abstract]   [Full Text] [Related]  

  • 24. State-dependent chemical reactivity of an engineered cysteine reveals conformational changes in the outer vestibule of the cystic fibrosis transmembrane conductance regulator.
    Zhang ZR; Song B; McCarty NA
    J Biol Chem; 2005 Dec; 280(51):41997-2003. PubMed ID: 16227620
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cystic fibrosis transmembrane conductance regulator: a chloride channel gated by ATP binding and hydrolysis.
    Bompadre SG; Hwang TC
    Sheng Li Xue Bao; 2007 Aug; 59(4):431-42. PubMed ID: 17700963
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Exploiting species differences to understand the CFTR Cl- channel.
    Bose SJ; Scott-Ward TS; Cai Z; Sheppard DN
    Biochem Soc Trans; 2015 Oct; 43(5):975-82. PubMed ID: 26517912
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Degenerate ABC composite site is stably glued together by trapped ATP.
    Csanády L
    J Gen Physiol; 2010 May; 135(5):395-8. PubMed ID: 20421369
    [No Abstract]   [Full Text] [Related]  

  • 28. Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel.
    Li C; Ramjeesingh M; Bear CE
    J Biol Chem; 1996 May; 271(20):11623-6. PubMed ID: 8662751
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. CFTR gating I: Characterization of the ATP-dependent gating of a phosphorylation-independent CFTR channel (DeltaR-CFTR).
    Bompadre SG; Ai T; Cho JH; Wang X; Sohma Y; Li M; Hwang TC
    J Gen Physiol; 2005 Apr; 125(4):361-75. PubMed ID: 15767295
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Strategies to investigate the mechanism of action of CFTR modulators.
    Cai Z; Scott-Ward TS; Li H; Schmidt A; Sheppard DN
    J Cyst Fibros; 2004 Aug; 3 Suppl 2():141-7. PubMed ID: 15463947
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Regulation of CFTR Cl- channel gating by ATP binding and hydrolysis.
    Ikuma M; Welsh MJ
    Proc Natl Acad Sci U S A; 2000 Jul; 97(15):8675-80. PubMed ID: 10880569
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Regulation of channel gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cells.
    Hallows KR; McCane JE; Kemp BE; Witters LA; Foskett JK
    J Biol Chem; 2003 Jan; 278(2):998-1004. PubMed ID: 12427743
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Partial rescue of F508del-cystic fibrosis transmembrane conductance regulator channel gating with modest improvement of protein processing, but not stability, by a dual-acting small molecule.
    Liu J; Bihler H; Farinha CM; Awatade NT; Romão AM; Mercadante D; Cheng Y; Musisi I; Jantarajit W; Wang Y; Cai Z; Amaral MD; Mense M; Sheppard DN
    Br J Pharmacol; 2018 Apr; 175(7):1017-1038. PubMed ID: 29318594
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator).
    Ramjeesingh M; Li C; Garami E; Huan LJ; Galley K; Wang Y; Bear CE
    Biochemistry; 1999 Feb; 38(5):1463-8. PubMed ID: 9931011
    [TBL] [Abstract][Full Text] [Related]  

  • 36. What we know and what we do not know about cystic fibrosis transmembrane conductance regulator.
    Ma J; Davis PB
    Clin Chest Med; 1998 Sep; 19(3):459-71, v-vi. PubMed ID: 9759549
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Structural mechanisms for defective CFTR gating caused by the Q1412X mutation, a severe Class VI pathogenic mutation in cystic fibrosis.
    Yeh JT; Yu YC; Hwang TC
    J Physiol; 2019 Jan; 597(2):543-560. PubMed ID: 30408177
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Voltage-dependent gating of the cystic fibrosis transmembrane conductance regulator Cl- channel.
    Cai Z; Scott-Ward TS; Sheppard DN
    J Gen Physiol; 2003 Nov; 122(5):605-20. PubMed ID: 14581585
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Synergistic Potentiation of Cystic Fibrosis Transmembrane Conductance Regulator Gating by Two Chemically Distinct Potentiators, Ivacaftor (VX-770) and 5-Nitro-2-(3-Phenylpropylamino) Benzoate.
    Lin WY; Sohma Y; Hwang TC
    Mol Pharmacol; 2016 Sep; 90(3):275-85. PubMed ID: 27413118
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.