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 *

128 related articles for article (PubMed ID: 33721574)

  • 1. Computational analysis of the effect of KCNH2 L532P mutation on ventricular electromechanical behaviors.
    Heikhmakhtiar AK; Dusturia N; Lim KM
    J Electrocardiol; 2021; 66():24-32. PubMed ID: 33721574
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Arrhythmic potency of human ether-a-go-go-related gene mutations L532P and N588K in a computational model of human atrial myocytes.
    Loewe A; Wilhelms M; Fischer F; Scholz EP; Dössel O; Seemann G
    Europace; 2014 Mar; 16(3):435-43. PubMed ID: 24569898
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Proarrhythmogenic Effect of the L532P and N588K
    Heikhmakhtiar AK; Abrha AT; Jeong DU; Lim KM
    J Korean Med Sci; 2020 Jul; 35(29):e238. PubMed ID: 32715669
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome.
    Adeniran I; McPate MJ; Witchel HJ; Hancox JC; Zhang H
    PLoS Comput Biol; 2011 Dec; 7(12):e1002313. PubMed ID: 22194679
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The hERG K(+) channel S4 domain L532P mutation: characterization at 37°C.
    Zhang YH; Colenso CK; Sessions RB; Dempsey CE; Hancox JC
    Biochim Biophys Acta; 2011 Oct; 1808(10):2477-87. PubMed ID: 21777565
    [TBL] [Abstract][Full Text] [Related]  

  • 6. In silico assessment of the effects of quinidine, disopyramide and E-4031 on short QT syndrome variant 1 in the human ventricles.
    Luo C; Wang K; Zhang H
    PLoS One; 2017; 12(6):e0179515. PubMed ID: 28632743
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Computational prediction of the effect of D172N KCNJ2 mutation on ventricular pumping during sinus rhythm and reentry.
    Heikhmakhtiar AK; Lee CH; Song KS; Lim KM
    Med Biol Eng Comput; 2020 May; 58(5):977-990. PubMed ID: 32095980
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Tbx20 controls the expression of the KCNH2 gene and of hERG channels.
    Caballero R; Utrilla RG; Amorós I; Matamoros M; Pérez-Hernández M; Tinaquero D; Alfayate S; Nieto-Marín P; Guerrero-Serna G; Liu QH; Ramos-Mondragón R; Ponce-Balbuena D; Herron T; Campbell KF; Filgueiras-Rama D; Peinado R; López-Sendón JL; Jalife J; Delpón E; Tamargo J
    Proc Natl Acad Sci U S A; 2017 Jan; 114(3):E416-E425. PubMed ID: 28049825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Differential effects of the β-adrenoceptor blockers carvedilol and metoprolol on SQT1- and SQT2-mutant channels.
    Bodi I; Franke G; Pantulu ND; Wu K; Perez-Feliz S; Bode C; Zehender M; zur Hausen A; Brunner M; Odening KE
    J Cardiovasc Electrophysiol; 2013 Oct; 24(10):1163-71. PubMed ID: 23718892
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The hERG channel activator, RPR260243, enhances protective
    Shi YP; Pang Z; Venkateshappa R; Gunawan M; Kemp J; Truong E; Chang C; Lin E; Shafaattalab S; Faizi S; Rayani K; Tibbits GF; Claydon VE; Claydon TW
    Am J Physiol Heart Circ Physiol; 2020 Aug; 319(2):H251-H261. PubMed ID: 32559136
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in KCNH2 yields loss-of-function of hERG potassium channel in long QT syndrome 2.
    Gu K; Qian D; Qin H; Cui C; Fernando WCHA; Wang D; Wang J; Cao K; Chen M
    Pflugers Arch; 2021 Feb; 473(2):219-229. PubMed ID: 33449212
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Influence of genetic mutations to atria vulnerability to atrial fibrillation: An in-silico 3D human atria study.
    Belletti R; Osca J; Romero Perez L; Saiz J
    Comput Methods Programs Biomed; 2024 Sep; 254():108307. PubMed ID: 38981143
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Computational Study to Identify the Effects of the KCNJ2 E299V Mutation in Cardiac Pumping Capacity.
    Jeong DU; Lee J; Lim KM
    Comput Math Methods Med; 2020; 2020():7194275. PubMed ID: 32328155
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Influence of the KCNQ1 S140G Mutation on Human Ventricular Arrhythmogenesis and Pumping Performance: Simulation Study.
    Jeong DU; Lim KM
    Front Physiol; 2018; 9():926. PubMed ID: 30108508
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Modulation of I(Kr) inactivation by mutation N588K in KCNH2: a link to arrhythmogenesis in short QT syndrome.
    Cordeiro JM; Brugada R; Wu YS; Hong K; Dumaine R
    Cardiovasc Res; 2005 Aug; 67(3):498-509. PubMed ID: 16039272
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional analysis of KCNH2 gene mutations of type 2 long QT syndrome in larval zebrafish using microscopy and electrocardiography.
    Tanaka Y; Hayashi K; Fujino N; Konno T; Tada H; Nakanishi C; Hodatsu A; Tsuda T; Nagata Y; Teramoto R; Yoshida S; Nomura A; Kawashiri MA; Yamagishi M
    Heart Vessels; 2019 Jan; 34(1):159-166. PubMed ID: 30047011
    [TBL] [Abstract][Full Text] [Related]  

  • 18. C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.
    Choe CU; Schulze-Bahr E; Neu A; Xu J; Zhu ZI; Sauter K; Bähring R; Priori S; Guicheney P; Mönnig G; Neapolitano C; Heidemann J; Clancy CE; Pongs O; Isbrandt D
    Hum Mol Genet; 2006 Oct; 15(19):2888-902. PubMed ID: 16923798
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice.
    Babij P; Askew GR; Nieuwenhuijsen B; Su CM; Bridal TR; Jow B; Argentieri TM; Kulik J; DeGennaro LJ; Spinelli W; Colatsky TJ
    Circ Res; 1998 Sep; 83(6):668-78. PubMed ID: 9742063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification through action potential clamp of proarrhythmic consequences of the short QT syndrome T618I hERG 'hotspot' mutation.
    Du C; Zhang H; Harmer SC; Hancox JC
    Biochem Biophys Res Commun; 2022 Mar; 596():49-55. PubMed ID: 35114584
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.