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 *

311 related articles for article (PubMed ID: 24958080)

  • 1. Cardiac sodium channel mutations: why so many phenotypes?
    Liu M; Yang KC; Dudley SC
    Nat Rev Cardiol; 2014 Oct; 11(10):607-15. PubMed ID: 24958080
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cardiac Sodium Channel Mutations: Why so Many Phenotypes?
    Liu M; Yang KC; Dudley SC
    Curr Top Membr; 2016; 78():513-59. PubMed ID: 27586294
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect.
    Niu DM; Hwang B; Hwang HW; Wang NH; Wu JY; Lee PC; Chien JC; Shieh RC; Chen YT
    J Med Genet; 2006 Oct; 43(10):817-21. PubMed ID: 16707561
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sodium channel mutations and arrhythmias.
    Ruan Y; Liu N; Priori SG
    Nat Rev Cardiol; 2009 May; 6(5):337-48. PubMed ID: 19377496
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
    Watanabe H; Koopmann TT; Le Scouarnec S; Yang T; Ingram CR; Schott JJ; Demolombe S; Probst V; Anselme F; Escande D; Wiesfeld AC; Pfeufer A; Kääb S; Wichmann HE; Hasdemir C; Aizawa Y; Wilde AA; Roden DM; Bezzina CR
    J Clin Invest; 2008 Jun; 118(6):2260-8. PubMed ID: 18464934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A sodium channel pore mutation causing Brugada syndrome.
    Pfahnl AE; Viswanathan PC; Weiss R; Shang LL; Sanyal S; Shusterman V; Kornblit C; London B; Dudley SC
    Heart Rhythm; 2007 Jan; 4(1):46-53. PubMed ID: 17198989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.
    Kyndt F; Probst V; Potet F; Demolombe S; Chevallier JC; Baro I; Moisan JP; Boisseau P; Schott JJ; Escande D; Le Marec H
    Circulation; 2001 Dec; 104(25):3081-6. PubMed ID: 11748104
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cardiac sodium channelopathies.
    Amin AS; Asghari-Roodsari A; Tan HL
    Pflugers Arch; 2010 Jul; 460(2):223-37. PubMed ID: 20091048
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cardiac sodium channel diseases.
    Napolitano C; Rivolta I; Priori SG
    Clin Chem Lab Med; 2003 Apr; 41(4):439-44. PubMed ID: 12747584
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy.
    Wilde AAM; Amin AS
    JACC Clin Electrophysiol; 2018 May; 4(5):569-579. PubMed ID: 29798782
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.
    Remme CA; Wilde AA; Bezzina CR
    Trends Cardiovasc Med; 2008 Apr; 18(3):78-87. PubMed ID: 18436145
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in cardiac sodium channels: clinical implications.
    Liu H; Clancy C; Cormier J; Kass R
    Am J Pharmacogenomics; 2003; 3(3):173-9. PubMed ID: 12814325
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.
    Smits JP; Koopmann TT; Wilders R; Veldkamp MW; Opthof T; Bhuiyan ZA; Mannens MM; Balser JR; Tan HL; Bezzina CR; Wilde AA
    J Mol Cell Cardiol; 2005 Jun; 38(6):969-81. PubMed ID: 15910881
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology.
    Abriel H
    J Mol Cell Cardiol; 2010 Jan; 48(1):2-11. PubMed ID: 19744495
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cardiac sodium channel mutation in atrial fibrillation.
    Ellinor PT; Nam EG; Shea MA; Milan DJ; Ruskin JN; MacRae CA
    Heart Rhythm; 2008 Jan; 5(1):99-105. PubMed ID: 18088563
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biology of cardiac sodium channel Nav1.5 expression.
    Rook MB; Evers MM; Vos MA; Bierhuizen MF
    Cardiovasc Res; 2012 Jan; 93(1):12-23. PubMed ID: 21937582
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
    Rook MB; Bezzina Alshinawi C; Groenewegen WA; van Gelder IC; van Ginneken AC; Jongsma HJ; Mannens MM; Wilde AA
    Cardiovasc Res; 1999 Dec; 44(3):507-17. PubMed ID: 10690282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.
    Cheng J; Van Norstrand DW; Medeiros-Domingo A; Valdivia C; Tan BH; Ye B; Kroboth S; Vatta M; Tester DJ; January CT; Makielski JC; Ackerman MJ
    Circ Arrhythm Electrophysiol; 2009 Dec; 2(6):667-76. PubMed ID: 20009079
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic overlap of cardiac sodium channelopathies: individual-specific or mutation-specific?
    Makita N
    Circ J; 2009 May; 73(5):810-7. PubMed ID: 19336922
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome.
    Zumhagen S; Veldkamp MW; Stallmeyer B; Baartscheer A; Eckardt L; Paul M; Remme CA; Bhuiyan ZA; Bezzina CR; Schulze-Bahr E
    PLoS One; 2013; 8(6):e67963. PubMed ID: 23840796
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.