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Page 1
Cardiac channelopathies: genetic and molecular mechanisms.
Abriel H, Zaklyazminskaya EV. Abriel H, et al. Among authors: zaklyazminskaya ev. Gene. 2013 Mar 15;517(1):1-11. doi: 10.1016/j.gene.2012.12.061. Epub 2012 Dec 22. Gene. 2013. PMID: 23266818 Review.
Complex genetic background in a large family with Brugada syndrome.
Saber S, Amarouch MY, Fazelifar AF, Haghjoo M, Emkanjoo Z, Alizadeh A, Houshmand M, Gavrilenko AV, Abriel H, Zaklyazminskaya EV. Saber S, et al. Among authors: zaklyazminskaya ev. Physiol Rep. 2015 Jan 27;3(1):e12256. doi: 10.14814/phy2.12256. Print 2015 Jan 1. Physiol Rep. 2015. PMID: 25626866 Free PMC article.
Simultaneous Non-Invasive Epicardial and Endocardial Mapping in Patients With Brugada Syndrome: New Insights Into Arrhythmia Mechanisms.
Rudic B, Chaykovskaya M, Tsyganov A, Kalinin V, Tülümen E, Papavassiliu T, Dösch C, Liebe V, Kuschyk J, Röger S, El-Battrawy I, Akin I, Yakovleva M, Zaklyazminskaya E, Shestak A, Kim S, Chmelevsky M, Borggrefe M. Rudic B, et al. J Am Heart Assoc. 2016 Nov 14;5(11):e004095. doi: 10.1161/JAHA.116.004095. J Am Heart Assoc. 2016. PMID: 27930354 Free PMC article.
Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5.
Wang Z, Vermij SH, Sottas V, Shestak A, Ross-Kaschitza D, Zaklyazminskaya EV, Hudmon A, Pitt GS, Rougier JS, Abriel H. Wang Z, et al. Among authors: zaklyazminskaya ev. Channels (Austin). 2020 Dec;14(1):268-286. doi: 10.1080/19336950.2020.1805999. Channels (Austin). 2020. PMID: 32815768 Free PMC article.
49 results