BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 22166675)

  • 1. The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome.
    Eldstrom J; Fedida D
    Expert Rev Mol Med; 2011 Dec; 13():e38. PubMed ID: 22166675
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 80(8):524-32. PubMed ID: 12185453
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Does hERG coassemble with a beta subunit? Evidence for roles of MinK and MiRP1.
    Anantharam A; Abbott GW
    Novartis Found Symp; 2005; 266():100-12; discussion 112-7, 155-8. PubMed ID: 16050264
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.
    Larsen LA; Andersen PS; Kanters J; Svendsen IH; Jacobsen JR; Vuust J; Wettrell G; Tranebjaerg L; Bathen J; Christiansen M
    Clin Chem; 2001 Aug; 47(8):1390-5. PubMed ID: 11468227
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular Cloning and Functional Expression of the Equine K+ Channel KV11.1 (Ether à Go-Go-Related/KCNH2 Gene) and the Regulatory Subunit KCNE2 from Equine Myocardium.
    Pedersen PJ; Thomsen KB; Olander ER; Hauser F; Tejada Mde L; Poulsen KL; Grubb S; Buhl R; Calloe K; Klaerke DA
    PLoS One; 2015; 10(9):e0138320. PubMed ID: 26376488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. HERG-F463L potassium channels linked to long QT syndrome reduce I(Kr) current by a trafficking-deficient mechanism.
    Yang HT; Sun CF; Cui CC; Xue XL; Zhang AF; Li HB; Wang DQ; Shu J
    Clin Exp Pharmacol Physiol; 2009 Aug; 36(8):822-7. PubMed ID: 19215240
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Acquired QT interval prolongation and HERG: implications for drug discovery and development.
    Finlayson K; Witchel HJ; McCulloch J; Sharkey J
    Eur J Pharmacol; 2004 Oct; 500(1-3):129-42. PubMed ID: 15464027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Discovery of a small molecule activator of the human ether-a-go-go-related gene (HERG) cardiac K+ channel.
    Kang J; Chen XL; Wang H; Ji J; Cheng H; Incardona J; Reynolds W; Viviani F; Tabart M; Rampe D
    Mol Pharmacol; 2005 Mar; 67(3):827-36. PubMed ID: 15548764
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HERG channel (dys)function revealed by dynamic action potential clamp technique.
    Berecki G; Zegers JG; Verkerk AO; Bhuiyan ZA; de Jonge B; Veldkamp MW; Wilders R; van Ginneken AC
    Biophys J; 2005 Jan; 88(1):566-78. PubMed ID: 15475579
    [TBL] [Abstract][Full Text] [Related]  

  • 11. KCNE2 protein is expressed in ventricles of different species, and changes in its expression contribute to electrical remodeling in diseased hearts.
    Jiang M; Zhang M; Tang DG; Clemo HF; Liu J; Holwitt D; Kasirajan V; Pond AL; Wettwer E; Tseng GN
    Circulation; 2004 Apr; 109(14):1783-8. PubMed ID: 15066947
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A pharmacokinetic-pharmacodynamic model for the quantitative prediction of dofetilide clinical QT prolongation from human ether-a-go-go-related gene current inhibition data.
    Jonker DM; Kenna LA; Leishman D; Wallis R; Milligan PA; Jonsson EN
    Clin Pharmacol Ther; 2005 Jun; 77(6):572-82. PubMed ID: 15961988
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.
    Gordon E; Panaghie G; Deng L; Bee KJ; Roepke TK; Krogh-Madsen T; Christini DJ; Ostrer H; Basson CT; Chung W; Abbott GW
    Cardiovasc Res; 2008 Jan; 77(1):98-106. PubMed ID: 18006462
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [DNA-based diagnostics of long QT syndrome].
    Berge KE; Haugaa KH; Anfinsen OG; Früh A; Hallerud M; Jonsrud C; Øyen N; Gjesdal K; Amlie JP; Leren TP
    Tidsskr Nor Laegeforen; 2005 Oct; 125(20):2783-6. PubMed ID: 16244680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].
    Zhao QH; Liu C; Lu LW; Lü GL; Liu H; Tang SB; Quan L; Cheng JD
    Fa Yi Xue Za Zhi; 2012 Oct; 28(5):337-41, 346. PubMed ID: 23213782
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mouse ERG K(+) channel clones reveal differences in protein trafficking and function.
    Lin EC; Moungey BM; Lim E; Concannon SP; Anderson CL; Kyle JW; Makielski JC; Balijepalli SY; January CT
    J Am Heart Assoc; 2014 Dec; 3(6):e001491. PubMed ID: 25497881
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.