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 *

259 related articles for article (PubMed ID: 11889015)

  • 21. Biophysical defects in voltage.gated sodium channels associated with long QT and Brugada syndromes.
    Jones DK; Ruben PC
    Channels (Austin); 2008; 2(2):70-80. PubMed ID: 18849657
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Arrhythmogenesis in the short-QT syndrome associated with combined HERG channel gating defects: a simulation study.
    Itoh H; Horie M; Ito M; Imoto K
    Circ J; 2006 Apr; 70(4):502-8. PubMed ID: 16565572
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cellular consequences of HERG mutations in the long QT syndrome: precursors to sudden cardiac death.
    Clancy CE; Rudy Y
    Cardiovasc Res; 2001 May; 50(2):301-13. PubMed ID: 11334834
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Proarrhythmic consequences of a KCNQ1 AKAP-binding domain mutation: computational models of whole cells and heterogeneous tissue.
    Saucerman JJ; Healy SN; Belik ME; Puglisi JL; McCulloch AD
    Circ Res; 2004 Dec; 95(12):1216-24. PubMed ID: 15528464
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cardiac Arrhythmias Related to Sodium Channel Dysfunction.
    Savio-Galimberti E; Argenziano M; Antzelevitch C
    Handb Exp Pharmacol; 2018; 246():331-354. PubMed ID: 28965168
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Computer simulation of wild-type and mutant human cardiac Na+ current.
    Vecchietti S; Rivolta I; Severi S; Napolitano C; Priori SG; Cavalcanti S
    Med Biol Eng Comput; 2006 Mar; 44(1-2):35-44. PubMed ID: 16929919
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy.
    van Hoeijen DA; Blom MT; Tan HL
    Expert Opin Pharmacother; 2014 Sep; 15(13):1875-87. PubMed ID: 24992280
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. Modeling tissue- and mutation- specific electrophysiological effects in the long QT syndrome: role of the Purkinje fiber.
    Iyer V; Sampson KJ; Kass RS
    PLoS One; 2014; 9(6):e97720. PubMed ID: 24892747
    [TBL] [Abstract][Full Text] [Related]  

  • 31. UltraRapid communications : vascular superoxide production by NAD(P)H OxidaseAssociation with endothelial dysfunction and clinical risk factors.
    Guzik TJ; West NE; Black E; McDonald D; Ratnatunga C; Pillai R; Channon KM
    Circ Res; 2000 May; 86(9):1008. PubMed ID: 10807875
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.
    Grant AO; Carboni MP; Neplioueva V; Starmer CF; Memmi M; Napolitano C; Priori S
    J Clin Invest; 2002 Oct; 110(8):1201-9. PubMed ID: 12393856
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Sinus Bradycardia in Carriers of the SCN5A-1795insD Mutation: Unraveling the Mechanism through Computer Simulations.
    Wilders R
    Int J Mol Sci; 2018 Feb; 19(2):. PubMed ID: 29473904
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Modelling and imaging cardiac repolarization abnormalities.
    Rudy Y
    J Intern Med; 2006 Jan; 259(1):91-106. PubMed ID: 16336517
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A mutant cardiac sodium channel with multiple biophysical defects associated with overlapping clinical features of Brugada syndrome and cardiac conduction disease.
    Shirai N; Makita N; Sasaki K; Yokoi H; Sakuma I; Sakurada H; Akai J; Kimura A; Hiraoka M; Kitabatake A
    Cardiovasc Res; 2002 Feb; 53(2):348-54. PubMed ID: 11827685
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Brugada syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization.
    Marangoni S; Di Resta C; Rocchetti M; Barile L; Rizzetto R; Summa A; Severi S; Sommariva E; Pappone C; Ferrari M; Benedetti S; Zaza A
    Cardiovasc Res; 2011 Sep; 91(4):606-16. PubMed ID: 21705349
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia.
    Clancy CE; Rudy Y
    Nature; 1999 Aug; 400(6744):566-9. PubMed ID: 10448858
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Electrical heterogeneity within the ventricular wall.
    Antzelevitch C; Fish J
    Basic Res Cardiol; 2001 Nov; 96(6):517-27. PubMed ID: 11770069
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families.
    Veldkamp MW; Wilders R; Baartscheer A; Zegers JG; Bezzina CR; Wilde AA
    Circ Res; 2003 May; 92(9):976-83. PubMed ID: 12676817
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.