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Journal Abstract Search

248 related items for PubMed ID: 8914737

  • 21. Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.
    Yoshida H, Horie M, Otani H, Kawashima T, Onishi Y, Sasayama S.
    Am J Med Genet; 2001 Feb 01; 98(4):348-52. PubMed ID: 11170080
    [Abstract] [Full Text] [Related]

  • 22. The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmia.
    Scherer CR, Lerche C, Decher N, Dennis AT, Maier P, Ficker E, Busch AE, Wollnik B, Steinmeyer K.
    Br J Pharmacol; 2002 Nov 01; 137(6):892-900. PubMed ID: 12411421
    [Abstract] [Full Text] [Related]

  • 23. Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.
    Chen J, Zou A, Splawski I, Keating MT, Sanguinetti MC.
    J Biol Chem; 1999 Apr 09; 274(15):10113-8. PubMed ID: 10187793
    [Abstract] [Full Text] [Related]

  • 24. Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.
    Sanguinetti MC, Curran ME, Spector PS, Keating MT.
    Proc Natl Acad Sci U S A; 1996 Mar 05; 93(5):2208-12. PubMed ID: 8700910
    [Abstract] [Full Text] [Related]

  • 25. Analysis of the human KCNH2(HERG) gene: identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion.
    Paulussen A, Yang P, Pangalos M, Verhasselt P, Marrannes R, Verfaille C, Vandenberk I, Crabbe R, Konings F, Luyten W, Armstrong M.
    Hum Mutat; 2000 May 05; 15(5):483. PubMed ID: 10790218
    [Abstract] [Full Text] [Related]

  • 26. RsaI and MaeI intragenic RFLPs in the human HERG gene.
    Fung D, Zhang L, French J, Bailey B, Trent RJ.
    Clin Genet; 1998 Jun 05; 53(6):504. PubMed ID: 9712545
    [No Abstract] [Full Text] [Related]

  • 27. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM, Timothy K, Fox J, Zhang L.
    Cardiol Rev; 1999 Jun 05; 7(1):44-55. PubMed ID: 10348966
    [Abstract] [Full Text] [Related]

  • 28. I(Kr): the hERG channel.
    Tseng GN.
    J Mol Cell Cardiol; 2001 May 05; 33(5):835-49. PubMed ID: 11343409
    [Abstract] [Full Text] [Related]

  • 29. Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
    Sanguinetti MC.
    Ann N Y Acad Sci; 1999 Apr 30; 868():406-13. PubMed ID: 10414310
    [Abstract] [Full Text] [Related]

  • 30. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
    Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z.
    Circulation; 2002 Feb 19; 105(7):794-9. PubMed ID: 11854117
    [Abstract] [Full Text] [Related]

  • 31. Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.
    Isbrandt D, Friederich P, Solth A, Haverkamp W, Ebneth A, Borggrefe M, Funke H, Sauter K, Breithardt G, Pongs O, Schulze-Bahr E.
    J Mol Med (Berl); 2002 Aug 19; 80(8):524-32. PubMed ID: 12185453
    [Abstract] [Full Text] [Related]

  • 32. Characterization of a novel missense mutation in the pore of HERG in a patient with long QT syndrome.
    Yoshida H, Horie M, Otani H, Takano M, Tsuji K, Kubota T, Fukunami M, Sasayama S.
    J Cardiovasc Electrophysiol; 1999 Sep 19; 10(9):1262-70. PubMed ID: 10517660
    [Abstract] [Full Text] [Related]

  • 33. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.
    Sanguinetti MC, Jiang C, Curran ME, Keating MT.
    Cell; 1995 Apr 21; 81(2):299-307. PubMed ID: 7736582
    [Abstract] [Full Text] [Related]

  • 34. Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel.
    Huang FD, Chen J, Lin M, Keating MT, Sanguinetti MC.
    Circulation; 2001 Aug 28; 104(9):1071-5. PubMed ID: 11524404
    [Abstract] [Full Text] [Related]

  • 35. Identification of a COOH-terminal segment involved in maturation and stability of human ether-a-go-go-related gene potassium channels.
    Akhavan A, Atanasiu R, Shrier A.
    J Biol Chem; 2003 Oct 10; 278(41):40105-12. PubMed ID: 12885765
    [Abstract] [Full Text] [Related]

  • 36. Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.
    Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA.
    Circulation; 1999 Mar 16; 99(10):1344-7. PubMed ID: 10077519
    [Abstract] [Full Text] [Related]

  • 37. Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2.
    Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M.
    Clin Genet; 2000 Feb 16; 57(2):125-30. PubMed ID: 10735633
    [Abstract] [Full Text] [Related]

  • 38. A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology.
    Roden DM, Balser JR.
    Cardiovasc Res; 1999 Nov 16; 44(2):242-6. PubMed ID: 10690299
    [No Abstract] [Full Text] [Related]

  • 39. HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects.
    Zhou Z, Gong Q, Epstein ML, January CT.
    J Biol Chem; 1998 Aug 14; 273(33):21061-6. PubMed ID: 9694858
    [Abstract] [Full Text] [Related]

  • 40. Is restoration of intracellular trafficking clinically feasible in the long QT syndrome?: The example of HERG mutations.
    Kaufman ES, Ficker E.
    J Cardiovasc Electrophysiol; 2003 Mar 14; 14(3):320-2. PubMed ID: 12716119
    [No Abstract] [Full Text] [Related]

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