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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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Valve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification

Journal of the American Heart Association, 2017-09, Vol.6 (9), p.n/a

2017

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Dose-dependent mechanism of Notch action in promoting osteogenic differentiation of mesenchymal stem cells

Cell and tissue research, 2020, Vol.379 (1), p.169-179

2020

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Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1601, p.79

2017

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Systematic dissection of biases in whole-exome and whole-genome sequencing reveals major determinants of coding sequence coverage

Scientific reports, 2020-02, Vol.10 (1), p.2057-2057, Article 2057

2020

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Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype

International journal of molecular sciences, 2021-07, Vol.22 (14), p.7349

2021

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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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Chicken rRNA Gene Cluster Structure

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

2016

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Notch signaling in the pathogenesis of thoracic aortic aneurysms: A bridge between embryonic and adult states

Biochimica et biophysica acta. Molecular basis of disease, 2020-03, Vol.1866 (3), p.165631-165631, Article 165631

2020

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Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing

PloS one, 2016-09, Vol.11 (9), p.e0163362-e0163362

2016

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Characterization of pathogenic genetic variants in Russian patients with primary ciliary dyskinesia using gene panel sequencing and transcript analysis

Orphanet journal of rare diseases, 2024-08, Vol.19 (1), p.310-23

2024

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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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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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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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Genotype imputation and polygenic score estimation in northwestern Russian population

PloS one, 2022-06, Vol.17 (6), p.e0269434-e0269434

2022

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Transgenerational and intergenerational effects of early childhood famine exposure in the cohort of offspring of Leningrad Siege survivors

Scientific reports, 2023-07, Vol.13 (1), p.11188-11188, Article 11188

2023

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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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Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments

PloS one, 2020-03, Vol.15 (3), p.e0229227-e0229227

2020

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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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Case Report: Loss-of-Function ABCC9 Genetic Variant Associated With Ventricular Fibrillation

Frontiers in genetics, 2022-04, Vol.13, p.718853

2022

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

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

2019

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Relationship Between Vitamin D Status and Vitamin D Receptor Gene Polymorphisms With Markers of Metabolic Syndrome Among Adults

Frontiers in endocrinology (Lausanne), 2018-08, Vol.9, p.448-448

2018

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SIGIRR gene variants in term newborns with congenital heart defects and necrotizing enterocolitis

Annals of pediatric cardiology, 2023-09, Vol.16 (5), p.337-344

2023

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In silico analysis of TRPM4 variants of unknown clinical significance

Biophysical mechanisms of myocardium sodium channelopathies

Valve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification

Dose-dependent mechanism of Notch action in promoting osteogenic differentiation of mesenchymal stem cells

Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness

Systematic dissection of biases in whole-exome and whole-genome sequencing reveals major determinants of coding sequence coverage

Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype

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

Chicken rRNA Gene Cluster Structure

Notch signaling in the pathogenesis of thoracic aortic aneurysms: A bridge between embryonic and adult states

Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing

Characterization of pathogenic genetic variants in Russian patients with primary ciliary dyskinesia using gene panel sequencing and transcript analysis

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

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

Intersegment Contacts of Potentially Damaging Variants of Cardiac Sodium Channel

Genotype imputation and polygenic score estimation in northwestern Russian population

Transgenerational and intergenerational effects of early childhood famine exposure in the cohort of offspring of Leningrad Siege survivors

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

Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments

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

Case Report: Loss-of-Function ABCC9 Genetic Variant Associated With Ventricular Fibrillation

Complex trait susceptibilities and population diversity in a sample of 4,145 Russians

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

Relationship Between Vitamin D Status and Vitamin D Receptor Gene Polymorphisms With Markers of Metabolic Syndrome Among Adults

SIGIRR gene variants in term newborns with congenital heart defects and necrotizing enterocolitis

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