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 *

211 related articles for article (PubMed ID: 23350853)

  • 21. Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.
    Ravn LS; Aizawa Y; Pollevick GD; Hofman-Bang J; Cordeiro JM; Dixen U; Jensen G; Wu Y; Burashnikov E; Haunso S; Guerchicoff A; Hu D; Svendsen JH; Christiansen M; Antzelevitch C
    Heart Rhythm; 2008 Mar; 5(3):427-35. PubMed ID: 18313602
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele.
    Hateley S; Lopez-Izquierdo A; Jou CJ; Cho S; Schraiber JG; Song S; Maguire CT; Torres N; Riedel M; Bowles NE; Arrington CB; Kennedy BJ; Etheridge SP; Lai S; Pribble C; Meyers L; Lundahl D; Byrnes J; Granka JM; Kauffman CA; Lemmon G; Boyden S; Scott Watkins W; Karren MA; Knight S; Brent Muhlestein J; Carlquist JF; Anderson JL; Chahine KG; Shah KU; Ball CA; Benjamin IJ; Yandell M; Tristani-Firouzi M
    Nat Commun; 2021 Nov; 12(1):6442. PubMed ID: 34750360
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation.
    Das S; Makino S; Melman YF; Shea MA; Goyal SB; Rosenzweig A; Macrae CA; Ellinor PT
    Heart Rhythm; 2009 Aug; 6(8):1146-53. PubMed ID: 19632626
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A molecular mechanism for adrenergic-induced long QT syndrome.
    Wu J; Naiki N; Ding WG; Ohno S; Kato K; Zang WJ; Delisle BP; Matsuura H; Horie M
    J Am Coll Cardiol; 2014 Mar; 63(8):819-27. PubMed ID: 24184248
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population.
    Chu HM; Feng MJ; Li YG; Zhang YX; Ma JF; He B; Yu YB; Liu J; Chen XM
    ScientificWorldJournal; 2013; 2013():373454. PubMed ID: 23710137
    [TBL] [Abstract][Full Text] [Related]  

  • 26. LQT1 mutations in KCNQ1 C-terminus assembly domain suppress IKs using different mechanisms.
    Aromolaran AS; Subramanyam P; Chang DD; Kobertz WR; Colecraft HM
    Cardiovasc Res; 2014 Dec; 104(3):501-11. PubMed ID: 25344363
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation.
    Abraham RL; Yang T; Blair M; Roden DM; Darbar D
    J Mol Cell Cardiol; 2010 Jan; 48(1):181-90. PubMed ID: 19646991
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [A novel KCNQ1 mutation in Chinese with congenital long QT syndrome].
    Liang L; Du ZD; Cai LL; Wu JX; Zheng T; Qi TX
    Zhonghua Er Ke Za Zhi; 2003 Oct; 41(10):724-7. PubMed ID: 14731347
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Effect of KCNQ1 G229D mutation on cardiac pumping efficacy and reentrant dynamics in ventricles: Computational study.
    Yuniarti AR; Setianto F; Marcellinus A; Hwang HJ; Choi SW; Trayanova N; Lim KM
    Int J Numer Method Biomed Eng; 2018 Jun; 34(6):e2970. PubMed ID: 29488358
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Gating mechanisms underlying deactivation slowing by two KCNQ1 atrial fibrillation mutations.
    Peng G; Barro-Soria R; Sampson KJ; Larsson HP; Kass RS
    Sci Rep; 2017 Apr; 7():45911. PubMed ID: 28383569
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
    Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
    J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cardiac arrhythmia and thyroid dysfunction: a novel genetic link.
    Purtell K; Roepke TK; Abbott GW
    Int J Biochem Cell Biol; 2010 Nov; 42(11):1767-70. PubMed ID: 20688187
    [TBL] [Abstract][Full Text] [Related]  

  • 33. KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
    Chen S; Zhang L; Bryant RM; Vincent GM; Flippin M; Lee JC; Brown E; Zimmerman F; Rozich R; Szafranski P; Oberti C; Sterba R; Marangi D; Tchou PJ; Chung MK; Wang Q
    Clin Genet; 2003 Apr; 63(4):273-82. PubMed ID: 12702160
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pro-arrhythmogenic effects of the S140G KCNQ1 mutation in human atrial fibrillation - insights from modelling.
    Kharche S; Adeniran I; Stott J; Law P; Boyett MR; Hancox JC; Zhang H
    J Physiol; 2012 Sep; 590(18):4501-14. PubMed ID: 22508963
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation.
    Benito B; Brugada R; Perich RM; Lizotte E; Cinca J; Mont L; Berruezo A; Tolosana JM; Freixa X; Brugada P; Brugada J
    Heart Rhythm; 2008 Oct; 5(10):1434-40. PubMed ID: 18929331
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Computational simulations of the effects of the G229D KCNQ1 mutation on human atrial fibrillation.
    Zulfa I; Shim EB; Song KS; Lim KM
    J Physiol Sci; 2016 Sep; 66(5):407-15. PubMed ID: 26922794
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Calmodulin is essential for cardiac IKS channel gating and assembly: impaired function in long-QT mutations.
    Shamgar L; Ma L; Schmitt N; Haitin Y; Peretz A; Wiener R; Hirsch J; Pongs O; Attali B
    Circ Res; 2006 Apr; 98(8):1055-63. PubMed ID: 16556865
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.
    Hong K; Bjerregaard P; Gussak I; Brugada R
    J Cardiovasc Electrophysiol; 2005 Apr; 16(4):394-6. PubMed ID: 15828882
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation.
    Horr S; Goldenberg I; Moss AJ; O-Uchi J; Barsheshet A; Connelly H; Gray DA; Zareba W; Lopes CM
    J Cardiovasc Electrophysiol; 2011 Feb; 22(2):193-200. PubMed ID: 20662986
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.
    Nielsen JB; Bentzen BH; Olesen MS; David JP; Olesen SP; Haunsø S; Svendsen JH; Schmitt N
    Biomark Med; 2014; 8(4):557-70. PubMed ID: 24796621
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.