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 *

80 related articles for article (PubMed ID: 18362023)

  • 1. Fetal arrhythmia caused by dysregulation of HERG channels.
    Grunnet M
    Heart Rhythm; 2008 Apr; 5(4):562-4. PubMed ID: 18362023
    [No Abstract]   [Full Text] [Related]  

  • 2. Distinct gene-specific mechanisms of arrhythmia revealed by cardiac gene transfer of two long QT disease genes, HERG and KCNE1.
    Hoppe UC; Marbán E; Johns DC
    Proc Natl Acad Sci U S A; 2001 Apr; 98(9):5335-40. PubMed ID: 11320260
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.
    Bhuiyan ZA; Momenah TS; Gong Q; Amin AS; Ghamdi SA; Carvalho JS; Homfray T; Mannens MM; Zhou Z; Wilde AA
    Heart Rhythm; 2008 Apr; 5(4):553-61. PubMed ID: 18362022
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM
    Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human ether-a-go-go related gene (hERG) K+ channels: function and dysfunction.
    Perrin MJ; Subbiah RN; Vandenberg JI; Hill AP
    Prog Biophys Mol Biol; 2008; 98(2-3):137-48. PubMed ID: 19027781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG.
    Hayashi K; Shimizu M; Ino H; Yamaguchi M; Terai H; Hoshi N; Higashida H; Terashima N; Uno Y; Kanaya H; Mabuchi H
    Clin Sci (Lond); 2004 Aug; 107(2):175-82. PubMed ID: 15043509
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutant MiRP1 subunits modulate HERG K+ channel gating: a mechanism for pro-arrhythmia in long QT syndrome type 6.
    Lu Y; Mahaut-Smith MP; Huang CL; Vandenberg JI
    J Physiol; 2003 Aug; 551(Pt 1):253-62. PubMed ID: 12923204
    [TBL] [Abstract][Full Text] [Related]  

  • 8. hERG potassium channels and cardiac arrhythmia.
    Sanguinetti MC; Tristani-Firouzi M
    Nature; 2006 Mar; 440(7083):463-9. PubMed ID: 16554806
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disopyramide is an effective inhibitor of mutant HERG K+ channels involved in variant 1 short QT syndrome.
    McPate MJ; Duncan RS; Witchel HJ; Hancox JC
    J Mol Cell Cardiol; 2006 Sep; 41(3):563-6. PubMed ID: 16842817
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.
    Paulussen AD; Raes A; Jongbloed RJ; Gilissen RA; Wilde AA; Snyders DJ; Smeets HJ; Aerssens J
    Cardiovasc Res; 2005 Aug; 67(3):467-75. PubMed ID: 15958262
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Progress in research on defective protein trafficking and functional restoration in HERG-associated long QT syndrome].
    Fang P; Lian J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):101-4. PubMed ID: 26829745
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
    Johnson WH; Yang P; Yang T; Lau YR; Mostella BA; Wolff DJ; Roden DM; Benson DW
    Pediatr Res; 2003 May; 53(5):744-8. PubMed ID: 12621127
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. Congenital and acquired long QT syndrome.
    Camm AJ; Janse MJ; Roden DM; Rosen MR; Cinca J; Cobbe SM
    Eur Heart J; 2000 Aug; 21(15):1232-7. PubMed ID: 10924312
    [No Abstract]   [Full Text] [Related]  

  • 15. hERG: protein trafficking and potential for therapy and drug side effects.
    Staudacher I; Schweizer PA; Katus HA; Thomas D
    Curr Opin Drug Discov Devel; 2010 Jan; 13(1):23-30. PubMed ID: 20047143
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ECGs in the ED.
    Tanel RE
    Pediatr Emerg Care; 2013 Jun; 29(6):778-9. PubMed ID: 23736078
    [No Abstract]   [Full Text] [Related]  

  • 17. Molecular genetic basis of sudden cardiac death.
    Towbin JA
    Pediatr Clin North Am; 2004 Oct; 51(5):1229-55. PubMed ID: 15331282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A family of hereditary long QT syndrome caused by Q738X HERG mutation.
    Yasuda S; Hiramatsu S; Odashiro K; Maruyama T; Tsuji K; Horie M
    Int J Cardiol; 2010 Sep; 144(1):69-72. PubMed ID: 19157587
    [No Abstract]   [Full Text] [Related]  

  • 19. Postmortem molecular screening in unexplained sudden death.
    Chugh SS; Senashova O; Watts A; Tran PT; Zhou Z; Gong Q; Titus JL; Hayflick SJ
    J Am Coll Cardiol; 2004 May; 43(9):1625-9. PubMed ID: 15120823
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Drugs, hERG and sudden death.
    Brown AM
    Cell Calcium; 2004 Jun; 35(6):543-7. PubMed ID: 15110144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.