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 *

135 related articles for article (PubMed ID: 9395071)

  • 1. Modulation of HERG affinity for E-4031 by [K+]o and C-type inactivation.
    Wang S; Morales MJ; Liu S; Strauss HC; Rasmusson RL
    FEBS Lett; 1997 Nov; 417(1):43-7. PubMed ID: 9395071
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A mutation in the pore region of HERG K+ channels expressed in Xenopus oocytes reduces rectification by shifting the voltage dependence of inactivation.
    Zou A; Xu QP; Sanguinetti MC
    J Physiol; 1998 May; 509 ( Pt 1)(Pt 1):129-37. PubMed ID: 9547387
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular determinants of inactivation and dofetilide block in ether a-go-go (EAG) channels and EAG-related K(+) channels.
    Ficker E; Jarolimek W; Brown AM
    Mol Pharmacol; 2001 Dec; 60(6):1343-8. PubMed ID: 11723241
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effects of outer mouth mutations on hERG channel function: a comparison with similar mutations in the Shaker channel.
    Fan JS; Jiang M; Dun W; McDonald TV; Tseng GN
    Biophys J; 1999 Jun; 76(6):3128-40. PubMed ID: 10354437
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Open channel block of HERG K(+) channels by vesnarinone.
    Kamiya K; Mitcheson JS; Yasui K; Kodama I; Sanguinetti MC
    Mol Pharmacol; 2001 Aug; 60(2):244-53. PubMed ID: 11455010
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Drug binding to aromatic residues in the HERG channel pore cavity as possible explanation for acquired Long QT syndrome by antiparkinsonian drug budipine.
    Scholz EP; Zitron E; Kiesecker C; Lueck S; Kathöfer S; Thomas D; Weretka S; Peth S; Kreye VA; Schoels W; Katus HA; Kiehn J; Karle CA
    Naunyn Schmiedebergs Arch Pharmacol; 2003 Nov; 368(5):404-14. PubMed ID: 14557918
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dissociation of E-4031 from the HERG channel caused by mutations of an amino acid results in greater block at high stimulation frequency.
    Ishii K; Nagai M; Takahashi M; Endoh M
    Cardiovasc Res; 2003 Mar; 57(3):651-9. PubMed ID: 12618227
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Extracellular sodium interacts with the HERG channel at an outer pore site.
    Mullins FM; Stepanovic SZ; Desai RR; George AL; Balser JR
    J Gen Physiol; 2002 Oct; 120(4):517-37. PubMed ID: 12356854
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Differential effects of bupivacaine on cardiac K channels: role of channel inactivation and subunit composition in drug-channel interaction.
    Lipka LJ; Jiang M; Tseng GN
    J Cardiovasc Electrophysiol; 1998 Jul; 9(7):727-42. PubMed ID: 9684721
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional characterization of the C-terminus of the human ether-à-go-go-related gene K(+) channel (HERG).
    Aydar E; Palmer C
    J Physiol; 2001 Jul; 534(Pt 1):1-14. PubMed ID: 11432987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interaction between tetraethylammonium and permeant cations at the inactivation gate of the HERG potassium channel.
    Shimizu H; Toyoshima C; Oiki S
    Jpn J Physiol; 2003 Feb; 53(1):25-34. PubMed ID: 12689355
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transfer of rapid inactivation and sensitivity to the class III antiarrhythmic drug E-4031 from HERG to M-eag channels.
    Herzberg IM; Trudeau MC; Robertson GA
    J Physiol; 1998 Aug; 511 ( Pt 1)(Pt 1):3-14. PubMed ID: 9679158
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Modulation of human ether-à-go-go-related K+ (HERG) channel inactivation by Cs+ and K+.
    Zhang S; Kehl SJ; Fedida D
    J Physiol; 2003 May; 548(Pt 3):691-702. PubMed ID: 12626667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structural and functional role of the extracellular s5-p linker in the HERG potassium channel.
    Liu J; Zhang M; Jiang M; Tseng GN
    J Gen Physiol; 2002 Nov; 120(5):723-37. PubMed ID: 12407082
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Time, voltage and ionic concentration dependence of rectification of h-erg expressed in Xenopus oocytes.
    Wang S; Morales MJ; Liu S; Strauss HC; Rasmusson RL
    FEBS Lett; 1996 Jul; 389(2):167-73. PubMed ID: 8766823
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inactivation gating determines nicotine blockade of human HERG channels.
    Wang HZ; Shi H; Liao SJ; Wang Z
    Am J Physiol; 1999 Sep; 277(3):H1081-8. PubMed ID: 10484431
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Altered gating of HERG potassium channels by cobalt and lanthanum.
    Sanchez-Chapula JA; Sanguinetti MC
    Pflugers Arch; 2000 Jun; 440(2):264-74. PubMed ID: 10898527
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation of transient Na+ conductance by intra- and extracellular K+ in the human delayed rectifier K+ channel Kv1.5.
    Wang Z; Zhang X; Fedida D
    J Physiol; 2000 Mar; 523 Pt 3(Pt 3):575-91. PubMed ID: 10718739
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High-affinity blockade of human ether-a-go-go-related gene human cardiac potassium channels by the novel antiarrhythmic drug BRL-32872.
    Thomas D; Wendt-Nordahl G; Röckl K; Ficker E; Brown AM; Kiehn J
    J Pharmacol Exp Ther; 2001 May; 297(2):753-61. PubMed ID: 11303067
    [TBL] [Abstract][Full Text] [Related]  

  • 20. State-dependent barium block of wild-type and inactivation-deficient HERG channels in Xenopus oocytes.
    Weerapura M; Nattel S; Courtemanche M; Doern D; Ethier N; Hebert T
    J Physiol; 2000 Jul; 526 Pt 2(Pt 2):265-78. PubMed ID: 10896755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.