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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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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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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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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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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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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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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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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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Mechanisms of Regenerative Potential Activation in Cardiac Mesenchymal Cells

Biomedicines, 2022-05, Vol.10 (6), p.1283

2022

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LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile

Genes, 2020-09, Vol.11 (9), p.1057

2020

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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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Relationship between the Levels of lncRNA H19 in Plasma and Different Adipose Tissue Depots with Patients' Response to Bariatric Surgery

Life (Basel, Switzerland), 2022-04, Vol.12 (5), p.633

2022

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Regulatory Action of Plasma from Patients with Obesity and Diabetes towards Muscle Cells Differentiation and Bioenergetics Revealed by the C2C12 Cell Model and MicroRNA Analysis

Biomolecules (Basel, Switzerland), 2021-05, Vol.11 (6), p.769

2021

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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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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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Effect of gene-lifestyle interaction on gestational diabetes risk

Oncotarget, 2017-12, Vol.8 (67), p.112024-112035

2017

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Functional properties of bone marrow derived multipotent mesenchymal stromal cells are altered in heart failure patients, and could be corrected by adjustment of expansion strategies

Aging (Albany, NY.), 2015-01, Vol.7 (1), p.14-25

2015

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Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve

Biochimica et biophysica acta, 2016-04, Vol.1862 (4), p.733-740

2016

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Arrhythmogenic Cardiomyopathy in 8-Year-Old Girl: Clinical Case. Difficult Path to Diagnosis

Pediatricheskai͡a︡ farmakologii͡a︡ : nauchno-prakticheskiĭ zhurnal Soi͡u︡za pediatrov Rossii, 2024-01, Vol.20 (6), p.574-579

2024

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Timothy Syndrome-Associated Mutations Affect State-Dependent Contacts in L-Type Calcium Channel

BIOPHYSICAL JOURNAL, 2019-02, Vol.116 (3), p.312a-312a

2019

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Association of tribbles homologue 1 gene expression in human umbilical vein endothelial cells with duration of intrauterine exposure to hyperglycaemia

Genetics Research, 2018-03, Vol.100, p.e3, Article e3

2018

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Next-generation DNA sequencing in an appropriate sex assignment: Case report of two phenotypically similar patients with 46, XY disorder of sex development

European Journal of Medical Case Reports, 2019, Vol.3 (2), p.68-73

2019

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Biophysical mechanisms of myocardium sodium channelopathies

In silico analysis of TRPM4 variants of unknown clinical significance

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

Chicken rRNA Gene Cluster Structure

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

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

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

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

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

Mechanisms of Regenerative Potential Activation in Cardiac Mesenchymal Cells

LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile

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

Relationship between the Levels of lncRNA H19 in Plasma and Different Adipose Tissue Depots with Patients' Response to Bariatric Surgery

Regulatory Action of Plasma from Patients with Obesity and Diabetes towards Muscle Cells Differentiation and Bioenergetics Revealed by the C2C12 Cell Model and MicroRNA Analysis

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

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

Effect of gene-lifestyle interaction on gestational diabetes risk

Functional properties of bone marrow derived multipotent mesenchymal stromal cells are altered in heart failure patients, and could be corrected by adjustment of expansion strategies

Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve

Arrhythmogenic Cardiomyopathy in 8-Year-Old Girl: Clinical Case. Difficult Path to Diagnosis

Timothy Syndrome-Associated Mutations Affect State-Dependent Contacts in L-Type Calcium Channel

Association of tribbles homologue 1 gene expression in human umbilical vein endothelial cells with duration of intrauterine exposure to hyperglycaemia

Next-generation DNA sequencing in an appropriate sex assignment: Case report of two phenotypically similar patients with 46, XY disorder of sex development

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