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

Frontiers in genetics, 2021-02, Vol.12, p.620337-620337

2021

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

International journal of molecular sciences, 2023-08, Vol.24 (15), p.12359

2023

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Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome

Frontiers in pharmacology, 2022-08, Vol.13, p.984299-984299

2022

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

Frontiers in genetics, 2021-09, Vol.12, p.722291-722291

2021

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

Genes, 2022-03, Vol.13 (4), p.559

2022

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Simultaneous Non‐Invasive Epicardial and Endocardial Mapping in Patients With Brugada Syndrome: New Insights Into Arrhythmia Mechanisms

Journal of the American Heart Association, 2016-11, Vol.5 (11), p.n/a

2016

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Three Myocardial Diseases in One Heart: Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Noncompaction and Myocarditis

Cardiogenetics, 2021-03, Vol.11 (1), p.18-27

2021

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Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening

Biochemistry (Moscow), 2024-03, Vol.89 (3), p.543-552

2024

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Mutational Spectrum of the SCN5A gene in Brugada Syndrome Patients

Journal of electrocardiology, 2019-03, Vol.53, p.e5-e6

2019

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Mutational Spectrum of the SCN5A gene in Brugada Syndrome Patients

Journal of electrocardiology, 2018-11, Vol.51 (6), p.1166-1166

2018

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

Biomedical reports, 2020-09, Vol.13 (3), p.1-16

2020

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Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5

Channels (Austin, Tex.), 2020-01, Vol.14 (1), p.268-286

2020

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

BMJ case reports, 2020-08, Vol.13 (8), p.e235703

2020

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Clinical Classification of Arrhythmogenic Right Ventricular Cardiomyopathy

Pulse (Basel), 2020-08, Vol.8 (1-2), p.21-30

2020

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Calmodulin binds to the N-terminal domain of the cardiac sodium channel Na v 1.5

Channels (Austin, Tex.), 2020-12, Vol.14 (1), p.268-286

2020

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Characterization of 2 Genetic Variants of Na v 1.5‐Arginine 689 Found in Patients with Cardiac Arrhythmias

Journal of cardiovascular electrophysiology, 2013-09, Vol.24 (9), p.1037-1046

2013

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Characterization of 2 Genetic Variants of Nav1.5-Arginine 689 Found in Patients with Cardiac Arrhythmias

Journal of cardiovascular electrophysiology, 2013-09, Vol.24 (9), p.1037-1046

2013

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Characterization of 2 genetic variants of Na(v) 1.5-arginine 689 found in patients with cardiac arrhythmias

Journal of cardiovascular electrophysiology, 2013-09, Vol.24 (9), p.1037-1046

2013

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Dilated cardiomyopathy with severe arrhythmias in Emery-Dreifuss muscular dystrophy: from ablation to heart transplantation

Journal of atrial fibrillation, 2016-12, Vol.9 (4), p.1468

2016

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Dilated cardiomyopathy with severe arrhythmias in Emery-Dreifuss muscular dystrophy: from ablation to heart transplantation

Journal of atrial fibrillation, 2016, Vol.9 (4), p.1468-1468

2016

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The Influence of Dimerization on the Pharmacokinetics and Activity of an Antibacterial Enzyme Lysostaphin

Molecules (Basel, Switzerland), 2019-05, Vol.24 (10), p.1879

2019

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Fusion of Lysostaphin to an Albumin Binding Domain Prolongs Its Half-Life and Bactericidal Activity in the Systemic Circulation

Molecules (Basel, Switzerland), 2019-08, Vol.24 (16), p.2892

2019

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The choice of chromatographic resin for the purification of recombinant lysostaphin affects its activity

Protein expression and purification, 2023-07, Vol.207, p.106274-106274, Article 106274

2023

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A Simple Protocol for the Determination of Lysostaphin Enzymatic Activity

Antibiotics (Basel), 2020-12, Vol.9 (12), p.917

2020

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FEATURES OF COST ADVANTAGES FROM IMPLEMENTATION OF ENERGY-SAVING PROJECTS

International journal of energy economics and policy, 2019, Vol.9 (3), p.53-58

2019

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

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

Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome

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

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

Simultaneous Non‐Invasive Epicardial and Endocardial Mapping in Patients With Brugada Syndrome: New Insights Into Arrhythmia Mechanisms

Three Myocardial Diseases in One Heart: Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Noncompaction and Myocarditis

Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening

Mutational Spectrum of the SCN5A gene in Brugada Syndrome Patients

Mutational Spectrum of the SCN5A gene in Brugada Syndrome Patients

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

Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5

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

Clinical Classification of Arrhythmogenic Right Ventricular Cardiomyopathy

Calmodulin binds to the N-terminal domain of the cardiac sodium channel Na v 1.5

Characterization of 2 Genetic Variants of Na v 1.5‐Arginine 689 Found in Patients with Cardiac Arrhythmias

Characterization of 2 Genetic Variants of Nav1.5-Arginine 689 Found in Patients with Cardiac Arrhythmias

Characterization of 2 genetic variants of Na(v) 1.5-arginine 689 found in patients with cardiac arrhythmias

Dilated cardiomyopathy with severe arrhythmias in Emery-Dreifuss muscular dystrophy: from ablation to heart transplantation

Dilated cardiomyopathy with severe arrhythmias in Emery-Dreifuss muscular dystrophy: from ablation to heart transplantation

The Influence of Dimerization on the Pharmacokinetics and Activity of an Antibacterial Enzyme Lysostaphin

Fusion of Lysostaphin to an Albumin Binding Domain Prolongs Its Half-Life and Bactericidal Activity in the Systemic Circulation

The choice of chromatographic resin for the purification of recombinant lysostaphin affects its activity

A Simple Protocol for the Determination of Lysostaphin Enzymatic Activity

FEATURES OF COST ADVANTAGES FROM IMPLEMENTATION OF ENERGY-SAVING PROJECTS

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