References analysis of the Wikipedia article "SCN5A" in the English version

doi.org

Catterall WA (2014). "Sodium channels, inherited epilepsy, and antiepileptic drugs". Annual Review of Pharmacology and Toxicology. 54: 317–338. doi:10.1146/annurev-pharmtox-011112-140232. PMID 24392695.

Remme CA, Verkerk AO, Hoogaars WM, Aanhaanen WT, Scicluna BP, Annink C, et al. (September 2009). "The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium". Basic Research in Cardiology. 104 (5): 511–522. doi:10.1007/s00395-009-0012-8. PMC 2722719. PMID 19255801.

Beyder A, Farrugia G (October 2016). "Ion channelopathies in functional GI disorders". American Journal of Physiology. Gastrointestinal and Liver Physiology. 311 (4): G581–G586. doi:10.1152/ajpgi.00237.2016. PMC 5142191. PMID 27514480.

Schroeter A, Walzik S, Blechschmidt S, Haufe V, Benndorf K, Zimmer T (July 2010). "Structure and function of splice variants of the cardiac voltage-gated sodium channel Na(v)1.5". Journal of Molecular and Cellular Cardiology. 49 (1): 16–24. doi:10.1016/j.yjmcc.2010.04.004. PMID 20398673.

Chen-Izu Y, Shaw RM, Pitt GS, Yarov-Yarovoy V, Sack JT, Abriel H, et al. (March 2015). "Na+ channel function, regulation, structure, trafficking and sequestration". The Journal of Physiology. 593 (6): 1347–1360. doi:10.1113/jphysiol.2014.281428. PMC 4376415. PMID 25772290.

Maltsev VA, Sabbah HN, Higgins RS, Silverman N, Lesch M, Undrovinas AI (December 1998). "Novel, ultraslow inactivating sodium current in human ventricular cardiomyocytes". Circulation. 98 (23): 2545–2552. doi:10.1161/01.cir.98.23.2545. PMID 9843461.

Sakmann BF, Spindler AJ, Bryant SM, Linz KW, Noble D (November 2000). "Distribution of a persistent sodium current across the ventricular wall in guinea pigs". Circulation Research. 87 (10): 910–914. doi:10.1161/01.res.87.10.910. PMID 11073887.

Attwell D, Cohen I, Eisner D, Ohba M, Ojeda C (March 1979). "The steady state TTX-sensitive ("window") sodium current in cardiac Purkinje fibres". Pflügers Archiv. 379 (2): 137–142. doi:10.1007/bf00586939. PMID 571107. S2CID 9145214.

Abriel H (January 2010). "Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology". Journal of Molecular and Cellular Cardiology. 48 (1): 2–11. doi:10.1016/j.yjmcc.2009.08.025. PMID 19744495.

Herren AW, Bers DM, Grandi E (August 2013). "Post-translational modifications of the cardiac Na channel: contribution of CaMKII-dependent phosphorylation to acquired arrhythmias". American Journal of Physiology. Heart and Circulatory Physiology. 305 (4): H431–H445. doi:10.1152/ajpheart.00306.2013. PMC 3891248. PMID 23771687.

Cerrone M, Lin X, Zhang M, Agullo-Pascual E, Pfenniger A, Chkourko Gusky H, et al. (March 2014). "Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype". Circulation. 129 (10): 1092–1103. doi:10.1161/CIRCULATIONAHA.113.003077. PMC 3954430. PMID 24352520.

Lodder EM, Bezzina CR (January 2014). "Genomics of cardiac electrical function". Briefings in Functional Genomics. 13 (1): 39–50. doi:10.1093/bfgp/elt029. PMID 23956259.

Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, et al. (March 1998). "Genetic basis and molecular mechanism for idiopathic ventricular fibrillation". Nature. 392 (6673): 293–296. Bibcode:1998Natur.392..293C. doi:10.1038/32675. PMID 9521325. S2CID 4315426.

Bezzina C, Veldkamp MW, van Den Berg MP, Postma AV, Rook MB, Viersma JW, et al. (December 1999). "A single Na(+) channel mutation causing both long-QT and Brugada syndromes". Circulation Research. 85 (12): 1206–1213. doi:10.1161/01.res.85.12.1206. PMID 10590249.

Remme CA, Verkerk AO, Nuyens D, van Ginneken AC, van Brunschot S, Belterman CN, et al. (December 2006). "Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD". Circulation. 114 (24): 2584–2594. doi:10.1161/CIRCULATIONAHA.106.653949. PMID 17145985. S2CID 10008930.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, et al. (September 1999). "Cardiac conduction defects associate with mutations in SCN5A". Nature Genetics. 23 (1): 20–21. doi:10.1038/12618. PMID 10471492. S2CID 7595466.

Tan HL, Bink-Boelkens MT, Bezzina CR, Viswanathan PC, Beaufort-Krol GC, van Tintelen PJ, et al. (February 2001). "A sodium-channel mutation causes isolated cardiac conduction disease". Nature. 409 (6823): 1043–1047. Bibcode:2001Natur.409.1043T. doi:10.1038/35059090. PMID 11234013. S2CID 4422570.

McNair WP, Ku L, Taylor MR, Fain PR, Dao D, Wolfel E, et al. (October 2004). "SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia". Circulation. 110 (15): 2163–2167. doi:10.1161/01.CIR.0000144458.58660.BB. PMID 15466643.

Laurent G, Saal S, Amarouch MY, Béziau DM, Marsman RF, Faivre L, et al. (July 2012). "Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy". Journal of the American College of Cardiology. 60 (2): 144–156. doi:10.1016/j.jacc.2012.02.052. PMID 22766342.

Benson DW, Wang DW, Dyment M, Knilans TK, Fish FA, Strieper MJ, et al. (October 2003). "Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)". The Journal of Clinical Investigation. 112 (7): 1019–1028. doi:10.1172/JCI18062. PMC 198523. PMID 14523039.

Makiyama T, Akao M, Shizuta S, Doi T, Nishiyama K, Oka Y, et al. (October 2008). "A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation". Journal of the American College of Cardiology. 52 (16): 1326–1334. doi:10.1016/j.jacc.2008.07.013. PMID 18929244.

Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, et al. (March 1995). "SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome". Cell. 80 (5): 805–811. doi:10.1016/0092-8674(95)90359-3. PMID 7889574. S2CID 15418443.

Mann SA, Castro ML, Ohanian M, Guo G, Zodgekar P, Sheu A, et al. (October 2012). "R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy". Journal of the American College of Cardiology. 60 (16): 1566–1573. doi:10.1016/j.jacc.2012.05.050. PMID 22999724.

Olson TM, Michels VV, Ballew JD, Reyna SP, Karst ML, Herron KJ, et al. (January 2005). "Sodium channel mutations and susceptibility to heart failure and atrial fibrillation". JAMA. 293 (4): 447–454. doi:10.1001/jama.293.4.447. PMC 2039897. PMID 15671429.

Verstraelen TE, Ter Bekke RM, Volders PG, Masclee AA, Kruimel JW (July 2015). "The role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disorders". Neurogastroenterology and Motility. 27 (7): 906–913. doi:10.1111/nmo.12569. PMID 25898860. S2CID 5055360.

Beyder A, Mazzone A, Strege PR, Tester DJ, Saito YA, Bernard CE, et al. (June 2014). "Loss-of-function of the voltage-gated sodium channel NaV1.5 (channelopathies) in patients with irritable bowel syndrome". Gastroenterology. 146 (7): 1659–1668. doi:10.1053/j.gastro.2014.02.054. PMC 4096335. PMID 24613995.

Milne JR, Hellestrand KJ, Bexton RS, Burnett PJ, Debbas NM, Camm AJ (February 1984). "Class 1 antiarrhythmic drugs--characteristic electrocardiographic differences when assessed by atrial and ventricular pacing". European Heart Journal. 5 (2): 99–107. doi:10.1093/oxfordjournals.eurheartj.a061633. PMID 6723689.

Balser JR (April 2001). "The cardiac sodium channel: gating function and molecular pharmacology". Journal of Molecular and Cellular Cardiology. 33 (4): 599–613. doi:10.1006/jmcc.2000.1346. PMID 11273715. S2CID 35893248.

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Lodder EM, Bezzina CR (January 2014). "Genomics of cardiac electrical function". Briefings in Functional Genomics. 13 (1): 39–50. doi:10.1093/bfgp/elt029. PMID 23956259.

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SCN5A (English Wikipedia)