171 related articles for article (PubMed ID: 30967788)
1. Investigating the Complex Arrhythmic Phenotype Caused by the Gain-of-Function Mutation KCNQ1-G229D.
Zhou X; Bueno-Orovio A; Schilling RJ; Kirkby C; Denning C; Rajamohan D; Burrage K; Tinker A; Rodriguez B; Harmer SC
Front Physiol; 2019; 10():259. PubMed ID: 30967788
[TBL] [Abstract][Full Text] [Related]
2. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.
Hasegawa K; Ohno S; Ashihara T; Itoh H; Ding WG; Toyoda F; Makiyama T; Aoki H; Nakamura Y; Delisle BP; Matsuura H; Horie M
Heart Rhythm; 2014 Jan; 11(1):67-75. PubMed ID: 24096004
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Human Atrial Arrhythmogenesis and Sinus Bradycardia in
Whittaker DG; Colman MA; Ni H; Hancox JC; Zhang H
Front Physiol; 2018; 9():1402. PubMed ID: 30337886
[TBL] [Abstract][Full Text] [Related]
5. A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation.
Ki CS; Jung CL; Kim HJ; Baek KH; Park SJ; On YK; Kim KS; Noh SJ; Youm JB; Kim JS; Cho H
Pflugers Arch; 2014 Mar; 466(3):529-40. PubMed ID: 23989646
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Electrophysiological properties of iPS cell-derived cardiomyocytes from a patient with long QT syndrome type 1 harboring the novel mutation M437V of KCNQ1.
Sogo T; Morikawa K; Kurata Y; Li P; Ichinose T; Yuasa S; Nozaki D; Miake J; Ninomiya H; Shimizu W; Fukuda K; Yamamoto K; Shirayoshi Y; Hisatome I
Regen Ther; 2016 Jun; 4():9-17. PubMed ID: 31245483
[TBL] [Abstract][Full Text] [Related]
8. Use of mutant-specific ion channel characteristics for risk stratification of long QT syndrome patients.
Jons C; O-Uchi J; Moss AJ; Reumann M; Rice JJ; Goldenberg I; Zareba W; Wilde AA; Shimizu W; Kanters JK; McNitt S; Hofman N; Robinson JL; Lopes CM
Sci Transl Med; 2011 Mar; 3(76):76ra28. PubMed ID: 21451124
[TBL] [Abstract][Full Text] [Related]
9. De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.
Hong K; Piper DR; Diaz-Valdecantos A; Brugada J; Oliva A; Burashnikov E; Santos-de-Soto J; Grueso-Montero J; Diaz-Enfante E; Brugada P; Sachse F; Sanguinetti MC; Brugada R
Cardiovasc Res; 2005 Dec; 68(3):433-40. PubMed ID: 16109388
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Arrhythmia formation in subclinical ("silent") long QT syndrome requires multiple insults: quantitative mechanistic study using the KCNQ1 mutation Q357R as example.
O'Hara T; Rudy Y
Heart Rhythm; 2012 Feb; 9(2):275-82. PubMed ID: 21952006
[TBL] [Abstract][Full Text] [Related]
12. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness.
Oertli A; Rinné S; Moss R; Kääb S; Seemann G; Beckmann BM; Decher N
Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33498651
[No Abstract] [Full Text] [Related]
13. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
Lupoglazoff JM; Denjoy I; Villain E; Fressart V; Simon F; Bozio A; Berthet M; Benammar N; Hainque B; Guicheney P
J Am Coll Cardiol; 2004 Mar; 43(5):826-30. PubMed ID: 14998624
[TBL] [Abstract][Full Text] [Related]
14. Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1.
Kubota T; Shimizu W; Kamakura S; Horie M
J Cardiovasc Electrophysiol; 2000 Sep; 11(9):1048-54. PubMed ID: 11021476
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Sudden death associated with QT interval prolongation and KCNQ1 gene mutation in a family of English Springer Spaniels.
Ware WA; Reina-Doreste Y; Stern JA; Meurs KM
J Vet Intern Med; 2015; 29(2):561-8. PubMed ID: 25779927
[TBL] [Abstract][Full Text] [Related]
17. Long QT syndrome caveolin-3 mutations differentially modulate K
Tyan L; Foell JD; Vincent KP; Woon MT; Mesquitta WT; Lang D; Best JM; Ackerman MJ; McCulloch AD; Glukhov AV; Balijepalli RC; Kamp TJ
J Physiol; 2019 Mar; 597(6):1531-1551. PubMed ID: 30588629
[TBL] [Abstract][Full Text] [Related]
18. Microscopic mechanisms for long QT syndrome type 1 revealed by single-channel analysis of I(Ks) with S3 domain mutations in KCNQ1.
Eldstrom J; Wang Z; Werry D; Wong N; Fedida D
Heart Rhythm; 2015 Feb; 12(2):386-94. PubMed ID: 25444851
[TBL] [Abstract][Full Text] [Related]
19. Computational Study on Effect of KCNQ1 P535T Mutation in a Cardiac Ventricular Tissue.
Satish H; Machireddy RR
J Membr Biol; 2023 Jun; 256(3):287-297. PubMed ID: 37166559
[TBL] [Abstract][Full Text] [Related]
20. R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.
Bartos DC; Duchatelet S; Burgess DE; Klug D; Denjoy I; Peat R; Lupoglazoff JM; Fressart V; Berthet M; Ackerman MJ; January CT; Guicheney P; Delisle BP
Heart Rhythm; 2011 Jan; 8(1):48-55. PubMed ID: 20850564
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
