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Features of Metadiscourse Use (Sphere of Economics, Students’ Written Texts in English)

Vestnik Tomskogo gosudarstvennogo universiteta. Filologiya, 2021-12 (74), p.188-207

2021

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New generation osteoprotectors as a means of restoring bone tissue against the background of vitamin D deficiency

Vrach, 2023-10, Vol.34 (9), p.73-78

2023

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Selective dechlorination of polychlorofluoroaromatic compounds: preparation of 1,3,5-trifluorobenzene

Journal of fluorine chemistry, 1999-06, Vol.96 (1), p.23-24

1999

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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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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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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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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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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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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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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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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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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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POS1332 ETANERCEPT-ASSOCIATED NEW ONSET UVEITIS IN PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS UNDER BIOLOGICAL THERAPY: SINGLE CENTER EXPERIENCE

Annals of the rheumatic diseases, 2021-06, Vol.80 (Suppl 1), p.948-948

2021

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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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Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene

Biochimica et biophysica acta. Molecular basis of disease, 2020-11, Vol.1866 (11), p.165915-165915, Article 165915

2020

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Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes

Cellular physiology and biochemistry, 2020-07, Vol.54 (4), p.696-706

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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Two New Cases of Hypertrophic Cardiomyopathy and Skeletal Muscle Features Associated with ALPK3 Homozygous and Compound Heterozygous Variants

Genes, 2020-10, Vol.11 (10), p.1201

2020

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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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Regulation of Ribosomal Protein Synthesis in Prokaryotes

Molecular biology (New York), 2021, Vol.55 (1), p.16-36

2021

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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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Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63 -Compound Heterozygous Variant

Frontiers in genetics, 2022-02, Vol.13, p.743472

2022

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The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis

Journal of cardiovascular development and disease, 2024-07, Vol.11 (7), p.226

2024

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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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RBM20 -Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart

Genes, 2021-01, Vol.12 (1), p.94

2021

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Features of Metadiscourse Use (Sphere of Economics, Students’ Written Texts in English)

New generation osteoprotectors as a means of restoring bone tissue against the background of vitamin D deficiency

Selective dechlorination of polychlorofluoroaromatic compounds: preparation of 1,3,5-trifluorobenzene

Biophysical mechanisms of myocardium sodium channelopathies

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

Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype

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

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

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

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

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

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

POS1332 ETANERCEPT-ASSOCIATED NEW ONSET UVEITIS IN PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS UNDER BIOLOGICAL THERAPY: SINGLE CENTER EXPERIENCE

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

Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene

Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes

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

Two New Cases of Hypertrophic Cardiomyopathy and Skeletal Muscle Features Associated with ALPK3 Homozygous and Compound Heterozygous Variants

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

Regulation of Ribosomal Protein Synthesis in Prokaryotes

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

Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63 -Compound Heterozygous Variant

The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis

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

RBM20 -Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart

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