Zaklyazminskaya EV - Search Results

1

Novel Mutation Glu98Lys in Cardiac Tropomyosin Alters Its Structure and Impairs Myocardial Relaxation.

Matyushenko AM, Nefedova VV, Kochurova AM, Kopylova GV, Koubassova NA, Shestak AG, Yampolskaya DS, Shchepkin DV, Kleymenov SY, Ryabkova NS, Katrukha IA, Bershitsky SY, Zaklyazminskaya EV, Tsaturyan AK, Levitsky DI. Matyushenko AM, et al. Among authors: zaklyazminskaya ev. Int J Mol Sci. 2023 Aug 2;24(15):12359. doi: 10.3390/ijms241512359. Int J Mol Sci. 2023. PMID: 37569730 Free PMC article.

2

[Brugada Syndrome: Possibilities of the Use of Noninvasive Electrocardiographic Mapping. A Case Report].

Chaykovskaya MK, Fetisova EA, Yakoleva MV, Kalinin VV, Zaklyazminskaya EV. Chaykovskaya MK, et al. Among authors: zaklyazminskaya ev. Kardiologiia. 2015;55(5):100-3. Kardiologiia. 2015. PMID: 26615633 Russian.

3

New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

Rogozhina Y, Mironovich S, Shestak A, Adyan T, Polyakov A, Podolyak D, Bakulina A, Dzemeshkevich S, Zaklyazminskaya E. Rogozhina Y, et al. Gene. 2016 Dec 31;595(2):202-206. doi: 10.1016/j.gene.2016.10.001. Epub 2016 Oct 4. Gene. 2016. PMID: 27717888

4

Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.

Golubenko M, Mikhailov V, Rusinova V, Shestak A, Zaklyazminskaya E. Golubenko M, et al. Biomed Rep. 2020 Sep;13(3):16. doi: 10.3892/br.2020.1324. Epub 2020 Jul 2. Biomed Rep. 2020. PMID: 32765855 Free PMC article.

5

Calmodulin binds to the N-terminal domain of the cardiac sodium channel Na_v1.5.

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.

6

Compound heterozygous mutations in KCNJ2 and KCNH2 in a patient with severe Andersen-Tawil syndrome.

Polyak ME, Shestak A, Podolyak D, Zaklyazminskaya E. Polyak ME, et al. BMJ Case Rep. 2020 Aug 25;13(8):e235703. doi: 10.1136/bcr-2020-235703. BMJ Case Rep. 2020. PMID: 32843460 Free PMC article.

7

Clinical Classification of Arrhythmogenic Right Ventricular Cardiomyopathy.

Lutokhina Y, Blagova O, Nedostup A, Alexandrova S, Shestak A, Zaklyazminskaya E. Lutokhina Y, et al. Pulse (Basel). 2020 Aug;8(1-2):21-30. doi: 10.1159/000505652. Epub 2020 Feb 11. Pulse (Basel). 2020. PMID: 32999875 Free PMC article.

8

Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels.

Shestak AG, Bukaeva AA, Saber S, Zaklyazminskaya EV. Shestak AG, et al. Among authors: zaklyazminskaya ev. Front Genet. 2021 Feb 1;12:620337. doi: 10.3389/fgene.2021.620337. eCollection 2021. Front Genet. 2021. PMID: 33633783 Free PMC article.

9

Coexistence of Two Rare Genetic Variants in Canonical and Non-canonical Exons of SCN5A: A Potential Source of Misinterpretation.

Shestak AG, Makarov LM, Komoliatova VN, Kolesnikova IV, Skorodumova LO, Generozov EV, Zaklyazminskaya EV. Shestak AG, et al. Among authors: zaklyazminskaya ev. Front Genet. 2021 Sep 6;12:722291. doi: 10.3389/fgene.2021.722291. eCollection 2021. Front Genet. 2021. PMID: 34552620 Free PMC article.

10

Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome.

Zaklyazminskaya E, Polyak M, Shestak A, Sadekova M, Komoliatova V, Kiseleva I, Makarov L, Podolyak D, Glukhov G, Zhang H, Abramochkin D, Sokolova OS. Zaklyazminskaya E, et al. Genes (Basel). 2022 Mar 22;13(4):559. doi: 10.3390/genes13040559. Genes (Basel). 2022. PMID: 35456365 Free PMC article.

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