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.
247 related articles for article (PubMed ID: 33712541)
1. Structure of human Na Li Z; Jin X; Wu T; Zhao X; Wang W; Lei J; Pan X; Yan N Proc Natl Acad Sci U S A; 2021 Mar; 118(11):. PubMed ID: 33712541 [TBL] [Abstract][Full Text] [Related]
2. Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. Veltmann C; Barajas-Martinez H; Wolpert C; Borggrefe M; Schimpf R; Pfeiffer R; Cáceres G; Burashnikov E; Antzelevitch C; Hu D J Am Heart Assoc; 2016 Jul; 5(7):. PubMed ID: 27381756 [TBL] [Abstract][Full Text] [Related]
3. Comparative structural analysis of human Na Pan X; Li Z; Jin X; Zhao Y; Huang G; Huang X; Shen Z; Cao Y; Dong M; Lei J; Yan N Proc Natl Acad Sci U S A; 2021 Mar; 118(11):. PubMed ID: 33712547 [TBL] [Abstract][Full Text] [Related]
4. E1784K, the most common Brugada syndrome and long-QT syndrome type 3 mutant, disrupts sodium channel inactivation through two separate mechanisms. Peters CH; Watkins AR; Poirier OL; Ruben PC J Gen Physiol; 2020 Sep; 152(9):. PubMed ID: 32569350 [TBL] [Abstract][Full Text] [Related]
5. Differential calcium sensitivity in Na Abdelsayed M; Baruteau AE; Gibbs K; Sanatani S; Krahn AD; Probst V; Ruben PC J Physiol; 2017 Sep; 595(18):6165-6186. PubMed ID: 28734073 [TBL] [Abstract][Full Text] [Related]
6. Lidocaine attenuation testing: An in vivo investigation of putative LQT3-associated variants in the SCN5A-encoded sodium channel. Anderson HN; Bos JM; Kapplinger JD; Meskill JM; Ye D; Ackerman MJ Heart Rhythm; 2017 Aug; 14(8):1173-1179. PubMed ID: 28412158 [TBL] [Abstract][Full Text] [Related]
7. Systematic ajmaline challenge in patients with long QT 3 syndrome caused by the most common mutation: a multicentre study. Hohmann S; Rudic B; Konrad T; Duncker D; König T; Tülümen E; Rostock T; Borggrefe M; Veltmann C Europace; 2017 Oct; 19(10):1723-1729. PubMed ID: 27915266 [TBL] [Abstract][Full Text] [Related]
8. Binding characteristics of calpastatin domain L to Na Zhang F; Xue Y; Su J; Xu X; Zhao Y; Liu Y; Hu H; Hao L Biochem Biophys Res Commun; 2022 Oct; 627():39-44. PubMed ID: 36007333 [TBL] [Abstract][Full Text] [Related]
9. The efficacy of Ranolazine on E1784K is altered by temperature and calcium. Abdelsayed M; Ruprai M; Ruben PC Sci Rep; 2018 Feb; 8(1):3643. PubMed ID: 29483621 [TBL] [Abstract][Full Text] [Related]
11. Cardiac sodium channel Nav1.5 mutations and cardiac arrhythmia. Song W; Shou W Pediatr Cardiol; 2012 Aug; 33(6):943-9. PubMed ID: 22460359 [TBL] [Abstract][Full Text] [Related]
12. Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A. Kanters JK; Yuan L; Hedley PL; Stoevring B; Jons C; Bloch Thomsen PE; Grunnet M; Christiansen M; Jespersen T Circ J; 2014; 78(5):1136-43. PubMed ID: 24599044 [TBL] [Abstract][Full Text] [Related]
13. Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes. Viswanathan PC; Bezzina CR; George AL; Roden DM; Wilde AA; Balser JR Circulation; 2001 Sep; 104(10):1200-5. PubMed ID: 11535580 [TBL] [Abstract][Full Text] [Related]
14. A distinct molecular mechanism by which phenytoin rescues a novel long QT 3 variant. Gando I; Campana C; Tan RB; Cecchin F; Sobie EA; Coetzee WA J Mol Cell Cardiol; 2020 Jul; 144():1-11. PubMed ID: 32339567 [TBL] [Abstract][Full Text] [Related]
15. A novel NaV1.5 voltage sensor mutation associated with severe atrial and ventricular arrhythmias. Wang HG; Zhu W; Kanter RJ; Silva JR; Honeywell C; Gow RM; Pitt GS J Mol Cell Cardiol; 2016 Mar; 92():52-62. PubMed ID: 26801742 [TBL] [Abstract][Full Text] [Related]
16. Differential thermosensitivity in mixed syndrome cardiac sodium channel mutants. Abdelsayed M; Peters CH; Ruben PC J Physiol; 2015 Sep; 593(18):4201-23. PubMed ID: 26131924 [TBL] [Abstract][Full Text] [Related]
17. The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. Makita N; Behr E; Shimizu W; Horie M; Sunami A; Crotti L; Schulze-Bahr E; Fukuhara S; Mochizuki N; Makiyama T; Itoh H; Christiansen M; McKeown P; Miyamoto K; Kamakura S; Tsutsui H; Schwartz PJ; George AL; Roden DM J Clin Invest; 2008 Jun; 118(6):2219-29. PubMed ID: 18451998 [TBL] [Abstract][Full Text] [Related]
18. Elementary mechanisms of calmodulin regulation of Na Kang PW; Chakouri N; Diaz J; Tomaselli GF; Yue DT; Ben-Johny M Proc Natl Acad Sci U S A; 2021 May; 118(21):. PubMed ID: 34021086 [TBL] [Abstract][Full Text] [Related]
19. Mechanistic insights into the interaction of cardiac sodium channel Na Xiong H; Bai X; Quan Z; Yu D; Zhang H; Zhang C; Liang L; Yao Y; Yang Q; Wang Z; Wang L; Huang Y; Li H; Ren X; Tu X; Ke T; Xu C; Wang QK Heart Rhythm; 2022 Mar; 19(3):478-489. PubMed ID: 34843967 [TBL] [Abstract][Full Text] [Related]
20. Depolarization of the conductance-voltage relationship in the NaV1.5 mutant, E1784K, is due to altered fast inactivation. Peters CH; Yu A; Zhu W; Silva JR; Ruben PC PLoS One; 2017; 12(9):e0184605. PubMed ID: 28898267 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]