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 *

197 related articles for article (PubMed ID: 22064211)

  • 1. Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia.
    Murphy LL; Moon-Grady AJ; Cuneo BF; Wakai RT; Yu S; Kunic JD; Benson DW; George AL
    Heart Rhythm; 2012 Apr; 9(4):590-7. PubMed ID: 22064211
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform.
    Wang T; Wehrens XH
    Heart Rhythm; 2012 Apr; 9(4):598-9. PubMed ID: 22138134
    [No Abstract]   [Full Text] [Related]  

  • 3. In utero diagnosis of long QT syndrome by magnetocardiography.
    Cuneo BF; Strasburger JF; Yu S; Horigome H; Hosono T; Kandori A; Wakai RT
    Circulation; 2013 Nov; 128(20):2183-91. PubMed ID: 24218437
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel.
    Wang DW; Crotti L; Shimizu W; Pedrazzini M; Cantu F; De Filippo P; Kishiki K; Miyazaki A; Ikeda T; Schwartz PJ; George AL
    Circ Arrhythm Electrophysiol; 2008 Dec; 1(5):370-8. PubMed ID: 19808432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant.
    Lin MT; Wu MH; Chang CC; Chiu SN; Thériault O; Huang H; Christé G; Ficker E; Chahine M
    Heart Rhythm; 2008 Nov; 5(11):1567-74. PubMed ID: 18848812
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.
    Wei J; Wang DW; Alings M; Fish F; Wathen M; Roden DM; George AL
    Circulation; 1999 Jun; 99(24):3165-71. PubMed ID: 10377081
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation.
    Makita N; Horie M; Nakamura T; Ai T; Sasaki K; Yokoi H; Sakurai M; Sakuma I; Otani H; Sawa H; Kitabatake A
    Circulation; 2002 Sep; 106(10):1269-74. PubMed ID: 12208804
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.
    Abriel H; Cabo C; Wehrens XH; Rivolta I; Motoike HK; Memmi M; Napolitano C; Priori SG; Kass RS
    Circ Res; 2001 Apr; 88(7):740-5. PubMed ID: 11304498
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo mutation in the SCN5A gene associated with early onset of sudden infant death.
    Wedekind H; Smits JP; Schulze-Bahr E; Arnold R; Veldkamp MW; Bajanowski T; Borggrefe M; Brinkmann B; Warnecke I; Funke H; Bhuiyan ZA; Wilde AA; Breithardt G; Haverkamp W
    Circulation; 2001 Sep; 104(10):1158-64. PubMed ID: 11535573
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The natural history of fetal long QT syndrome.
    Cuneo BF; Strasburger JF; Wakai RT
    J Electrocardiol; 2016; 49(6):807-813. PubMed ID: 27539165
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.
    Vatta M; Ackerman MJ; Ye B; Makielski JC; Ughanze EE; Taylor EW; Tester DJ; Balijepalli RC; Foell JD; Li Z; Kamp TJ; Towbin JA
    Circulation; 2006 Nov; 114(20):2104-12. PubMed ID: 17060380
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.
    Keller DI; Acharfi S; Delacrétaz E; Benammar N; Rotter M; Pfammatter JP; Fressart V; Guicheney P; Chahine M
    J Mol Cell Cardiol; 2003 Dec; 35(12):1513-21. PubMed ID: 14654377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Arrhythmogenic consequences of Na+ channel mutations in the transmurally heterogeneous mammalian left ventricle: analysis of the I1768V SCN5A mutation.
    Flaim SN; Giles WR; McCulloch AD
    Heart Rhythm; 2007 Jun; 4(6):768-78. PubMed ID: 17556201
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations.
    Shinlapawittayatorn K; Du XX; Liu H; Ficker E; Kaufman ES; Deschênes I
    Heart Rhythm; 2011 Mar; 8(3):455-62. PubMed ID: 21109022
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.
    Lupoglazoff JM; Cheav T; Baroudi G; Berthet M; Denjoy I; Cauchemez B; Extramiana F; Chahine M; Guicheney P
    Circ Res; 2001 Jul; 89(2):E16-21. PubMed ID: 11463728
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.
    Tester DJ; Valdivia C; Harris-Kerr C; Alders M; Salisbury BA; Wilde AA; Makielski JC; Ackerman MJ
    Heart Rhythm; 2010 Jul; 7(7):912-9. PubMed ID: 20403459
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine.
    Valdivia CR; Ackerman MJ; Tester DJ; Wada T; McCormack J; Ye B; Makielski JC
    Cardiovasc Res; 2002 Aug; 55(2):279-89. PubMed ID: 12123767
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C
    J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels.
    Huang H; Priori SG; Napolitano C; O'Leary ME; Chahine M
    Am J Physiol Heart Circ Physiol; 2011 Jan; 300(1):H288-99. PubMed ID: 21076026
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.
    Hu RM; Tan BH; Orland KM; Valdivia CR; Peterson A; Pu J; Makielski JC
    Am J Physiol Heart Circ Physiol; 2013 Apr; 304(7):H994-H1001. PubMed ID: 23376825
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.