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Amarouch, Mohamed-Yassine; Zaklyazminskaya, Elena V; Rougier, Jean-Sébastien (2021). Editorial: Inherited Arrhythmias of the Cardiac Sodium Channel Nav1.5. Frontiers in physiology, 12, p. 716553. Frontiers Research Foundation 10.3389/fphys.2021.716553
Wang, Zizun; Vermij, Sarah H.; Sottas, Valentin; Shestak, Anna; Ross-Kaschitza, Daniela; Zaklyazminskaya, Elena V; Hudmon, Andy; Pitt, Geoffrey S; Rougier, Jean-Sébastien; Abriel, Hugues (2020). Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5. Channels, 14(1), pp. 268-286. Taylor & Francis 10.1080/19336950.2020.1805999
Saber, Siamak; Amarouch, Mohamed Yassine; Fazelifar, Amir-Farjam; Haghjoo, Majid; Emkanjoo, Zahra; Alizadeh, Abolfath; Houshmand, Massoud; Gavrilenko, Alexander V; Abriel, Hugues; Zaklyazminskaya, Elena V (2015). Complex genetic background in a large family with Brugada syndrome. Physiological reports, 3(1) The American Physiological Society 10.14814/phy2.12256
Abriel, Hugues; Zaklyazminskaya, Elena V (2013). Cardiac channelopathies: genetic and molecular mechanisms. Gene, 517(1), pp. 1-11. Amsterdam: Elsevier 10.1016/j.gene.2012.12.061
Zaklyazminskaya, Elena V; Abriel, Hugues (2012). Prevalence of Significant Genetic Variants in Congenital Long QT Syndrome is Largely Underestimated. Frontiers in Pharmacology, 3, p. 72. Frontiers 10.3389/fphar.2012.00072
Abriel, Hugues; Zaklyazminskaya, Elena V (2012). A modern approach to classify missense mutations in cardiac channelopathy genes. Circulation - cardiovascular genetics, 5(5), pp. 487-9. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1161/CIRCGENETICS.112.964809
