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In silico analysis of TRPM4 variants of unknown clinical significance

PloS one, 2023-12, Vol.18 (12), p.e0295974-e0295974

2023

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Biophysical mechanisms of myocardium sodium channelopathies

Pflügers Archiv, 2024-05, Vol.476 (5), p.735-753

2024

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Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner

Cell and tissue research, 2023-08, Vol.393 (2), p.357-375

2023

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Flnc expression impacts mitochondrial function, autophagy, and calcium handling in C2C12 cells

Experimental cell research, 2024-09, Vol.442 (1), p.114174, Article 114174

2024

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Distinct molecular features of FLNC mutations, associated with different clinical phenotypes

Cytoskeleton (Hoboken, N.J.), 2024-09

2024

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Association of Common Genetic Risk Variants With Gestational Diabetes Mellitus and Their Role in GDM Prediction

Frontiers in endocrinology (Lausanne), 2021-04, Vol.12, p.628582-628582

2021

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Possible Interactions of Extracellular Loop IVP2-S6 With Voltage-Sensing Domain III in Cardiac Sodium Channel

Frontiers in pharmacology, 2021-10, Vol.12, p.742508-742508

2021

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Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood

Orphanet journal of rare diseases, 2022-09, Vol.17 (1), p.1-358, Article 358

2022

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Intersegment Contacts of Potentially Damaging Variants of Cardiac Sodium Channel

Frontiers in pharmacology, 2021-11, Vol.12, p.756415-756415

2021

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L-Type Calcium Channel: Predicting Pathogenic/Likely Pathogenic Status for Variants of Uncertain Clinical Significance

Membranes (Basel), 2021-08, Vol.11 (8), p.599

2021

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Chicken rRNA Gene Cluster Structure

PloS one, 2016-06, Vol.11 (6), p.e0157464-e0157464

2016

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Atomic Mechanisms of Timothy Syndrome-Associated Mutations in Calcium Channel Cav1.2

Frontiers in physiology, 2019-03, Vol.10, p.335-335

2019

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Analysis of Slow Inactivation of Nav1.5 Channels in the Development of Hereditary Heart Pathology

Cell and tissue biology, 2024, Vol.18 (3), p.324-333

2024

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Left ventricular non - compaction: contemporary view of genetic background, clinical course, diagnostic and treatment

Terapevtic̆eskii arhiv, 2019-12, Vol.91 (12), p.90-97

2019

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Different Notch signaling in cells from calcified bicuspid and tricuspid aortic valves

Journal of molecular and cellular cardiology, 2018-01, Vol.114, p.211-219

2018

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Characterization of a novel SCN5A genetic variant A1294G associated with mixed clinical phenotype

Biochemical and biophysical research communications, 2019-08, Vol.516 (3), p.777-783

2019

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Electrophysiology of the Danio rerio Heart

Biochemistry (Moscow). Supplement series A, Membrane and cell biology, 2024-06, Vol.18 (2), p.55-69

2024

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Clinical Response to Personalized Exercise Therapy in Heart Failure Patients with Reduced Ejection Fraction is Accompanied by Skeletal Muscle Histological Alterations

International journal of molecular sciences, 2019-11, Vol.20 (21), p.5514

2019

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Lamin A/C mutation associated with lipodystrophy influences adipogenic differentiation of stem cells through interaction with Notch signaling

Biochemistry and cell biology, 2018-06, Vol.96 (3), p.342-348

2018

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Skeletal Muscle Resident Progenitor Cells Coexpress Mesenchymal and Myogenic Markers and Are Not Affected by Chronic Heart Failure-Induced Dysregulations

Stem cells international, 2019-01, Vol.2019 (2019), p.1-11

2019

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Extracellular MicroRNAs and Mitochondrial DNA as Potential Biomarkers of Arrhythmogenic Cardiomyopathy

Biochemistry (Moscow), 2019-03, Vol.84 (3), p.272-282

2019

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Different Expressions of Pericardial Fluid MicroRNAs in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy and Ischemic Heart Disease Undergoing Ventricular Tachycardia Ablation

Frontiers in cardiovascular medicine, 2021-03, Vol.8, p.647812-647812

2021

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Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome

Biochemistry and biophysics reports, 2022-07, Vol.30, p.101249, Article 101249

2022

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miR-21, miR-93, miR-191, miR-let-7b, and miR-499 Expression Level in Plasma and Cerebrospinal Fluid in Patients with Prolonged Disorders of Consciousness

Neurology international, 2022-12, Vol.15 (1), p.40-54

2022

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Hypertrophic cardiomyopathy: modern aspects of pharmacologic treatment

Terapevtic̆eskii arhiv, 2019-09, Vol.91 (9), p.129-136

2019

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In silico analysis of TRPM4 variants of unknown clinical significance

Biophysical mechanisms of myocardium sodium channelopathies

Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner

Flnc expression impacts mitochondrial function, autophagy, and calcium handling in C2C12 cells

Distinct molecular features of FLNC mutations, associated with different clinical phenotypes

Association of Common Genetic Risk Variants With Gestational Diabetes Mellitus and Their Role in GDM Prediction

Possible Interactions of Extracellular Loop IVP2-S6 With Voltage-Sensing Domain III in Cardiac Sodium Channel

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood

Intersegment Contacts of Potentially Damaging Variants of Cardiac Sodium Channel

L-Type Calcium Channel: Predicting Pathogenic/Likely Pathogenic Status for Variants of Uncertain Clinical Significance

Chicken rRNA Gene Cluster Structure

Atomic Mechanisms of Timothy Syndrome-Associated Mutations in Calcium Channel Cav1.2

Analysis of Slow Inactivation of Nav1.5 Channels in the Development of Hereditary Heart Pathology

Left ventricular non - compaction: contemporary view of genetic background, clinical course, diagnostic and treatment

Different Notch signaling in cells from calcified bicuspid and tricuspid aortic valves

Characterization of a novel SCN5A genetic variant A1294G associated with mixed clinical phenotype

Electrophysiology of the Danio rerio Heart

Clinical Response to Personalized Exercise Therapy in Heart Failure Patients with Reduced Ejection Fraction is Accompanied by Skeletal Muscle Histological Alterations

Lamin A/C mutation associated with lipodystrophy influences adipogenic differentiation of stem cells through interaction with Notch signaling

Skeletal Muscle Resident Progenitor Cells Coexpress Mesenchymal and Myogenic Markers and Are Not Affected by Chronic Heart Failure-Induced Dysregulations

Extracellular MicroRNAs and Mitochondrial DNA as Potential Biomarkers of Arrhythmogenic Cardiomyopathy

Different Expressions of Pericardial Fluid MicroRNAs in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy and Ischemic Heart Disease Undergoing Ventricular Tachycardia Ablation

Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome

miR-21, miR-93, miR-191, miR-let-7b, and miR-499 Expression Level in Plasma and Cerebrospinal Fluid in Patients with Prolonged Disorders of Consciousness

Hypertrophic cardiomyopathy: modern aspects of pharmacologic treatment

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