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Clinical Genetic Characteristics of Epilepsy Due to Mutations in the PCDH19 Gene (OMIM: 300088)

Neuroscience and behavioral physiology, 2020-11, Vol.50 (9), p.1099-1104

2020

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Role of Molecular Genetic Factors in Formation of the Clinical Type of Neurofibromatosis Type 2

Russian journal of genetics, 2024-02, Vol.60 (2), p.210-219

2024

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Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7

International journal of molecular sciences, 2021-06, Vol.22 (12), p.6318

2021

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Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report

International journal of molecular sciences, 2023-03, Vol.24 (5), p.4515

2023

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The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies

International journal of molecular sciences, 2018-12, Vol.19 (12), p.3975

2018

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Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln147Pro Tropomyosin

International journal of molecular sciences, 2020-10, Vol.21 (20), p.7590

2020

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Molecular Mechanisms of Muscle Weakness Associated with E173A Mutation in Tpm3.12. Troponin Ca2+ Sensitivity Inhibitor W7 Can Reduce the Damaging Effect of This Mutation

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4421

2020

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The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2

Biochemical and biophysical research communications, 2020-02, Vol.523 (1), p.258-262

2020

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Physicochemical Conditions of Formation of Productive Mineral Assemblages of Gold Deposits in the Taimyr–Severnaya Zemlya Orogen

Doklady earth sciences, 2022-12, Vol.507 (Suppl 3), p.S375-S381

2022

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The molecular mechanisms of a high Ca2+-sensitivity and muscle weakness associated with the Ala155Thr substitution in Tpm3.12

Biochemical and biophysical research communications, 2019-07, Vol.515 (2), p.372-377

2019

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The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)

Russian geology and geophysics, 2018-08, Vol.59 (8), p.945-961

2018

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Physicochemical Conditions of Ore Formation at the Kalguty Mo–W Deposit: Thermodynamic Modeling

Geochemistry international, 2020, Vol.58 (1), p.27-39

2020

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Model for Prediction of Testing Time of a Computer Program for Automated Reliability Evaluation of Semiconductor Devices

Doklady Belorusskogo gosudarstvennogo universiteta informatiki i radioèlektroniki, 2022-12, Vol.20 (7), p.72-80

2022

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Influence of 2,3-Butanedione Monoxime on the Actin–Myosin Interaction in Modeling Healthy Function and Congenital Myopathy in a Single Muscle Fiber

Cell and tissue biology, 2023-04, Vol.17 (2), p.169-178

2023

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Deviations in conformational rearrangements of thin filaments and myosin caused by the Ala155Thr substitution in hydrophobic core of tropomyosin

Biochimica et biophysica acta. Proteins and proteomics, 2017-12, Vol.1865 (12), p.1790-1799

2017

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A Hybrid Simulation Model for VSC HVDC

IEEE transactions on smart grid, 2016-09, Vol.7 (5), p.2242-2249

2016

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Transcription profile analysis of the endometrium revealed molecular markers of the personalized 'window of implantation' during in vitro fertilization

Gynecological endocrinology, 2017-12, Vol.33 (sup1), p.22-27

2017

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Individual prediction of the reliability of high power transistors for electronic devices of medical purposes

Doklady Belorusskogo gosudarstvennogo universiteta informatiki i radioèlektroniki, 2021-02, Vol.19 (1), p.88-95

2021

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Heuristic Model of Forecasting of Operating State of Semiconductor Devices

Doklady Belorusskogo gosudarstvennogo universiteta informatiki i radioèlektroniki, 2022-03, Vol.20 (1), p.92-100

2022

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The reason for a high Ca2+-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycle

Biochemical and biophysical research communications, 2017-12, Vol.494 (3-4), p.681-686

2017

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The primary cause of muscle disfunction associated with substitutions E240K and R244G in tropomyosin is aberrant behavior of tropomyosin and response of actin and myosin during ATPase cycle

Archives of biochemistry and biophysics, 2018-04, Vol.644, p.17-28

2018

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Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle

Biochimica et biophysica acta, 2016-03, Vol.1864 (3), p.260-267

2016

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Accelerated Testing of High Power Transistors for Long Operation when Solving Problems of Prediction of their Reliability by the Method of Imitation Simulation

Doklady Belorusskogo gosudarstvennogo universiteta informatiki i radioèlektroniki, 2022-06, Vol.20 (4), p.36-43

2022

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Hard- and software simulation tools of emergency control system of turbine frequency and power regulators

Automation and remote control, 2017-11, Vol.78 (11), p.2085-2092

2017

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The reason for the low Ca2+-sensitivity of thin filaments associated with the Glu41Lys mutation in the TPM2 gene is “freezing” of tropomyosin near the outer domain of actin and inhibition of actin monomer switching off during the ATPase cycle

Biochemical and biophysical research communications, 2018-07, Vol.502 (2), p.209-214

2018

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Clinical Genetic Characteristics of Epilepsy Due to Mutations in the PCDH19 Gene (OMIM: 300088)

Role of Molecular Genetic Factors in Formation of the Clinical Type of Neurofibromatosis Type 2

Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7

Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report

The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies

Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln147Pro Tropomyosin

Molecular Mechanisms of Muscle Weakness Associated with E173A Mutation in Tpm3.12. Troponin Ca2+ Sensitivity Inhibitor W7 Can Reduce the Damaging Effect of This Mutation

The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2

Physicochemical Conditions of Formation of Productive Mineral Assemblages of Gold Deposits in the Taimyr–Severnaya Zemlya Orogen

The molecular mechanisms of a high Ca2+-sensitivity and muscle weakness associated with the Ala155Thr substitution in Tpm3.12

The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)

Physicochemical Conditions of Ore Formation at the Kalguty Mo–W Deposit: Thermodynamic Modeling

Model for Prediction of Testing Time of a Computer Program for Automated Reliability Evaluation of Semiconductor Devices

Influence of 2,3-Butanedione Monoxime on the Actin–Myosin Interaction in Modeling Healthy Function and Congenital Myopathy in a Single Muscle Fiber

Deviations in conformational rearrangements of thin filaments and myosin caused by the Ala155Thr substitution in hydrophobic core of tropomyosin

A Hybrid Simulation Model for VSC HVDC

Transcription profile analysis of the endometrium revealed molecular markers of the personalized 'window of implantation' during in vitro fertilization

Individual prediction of the reliability of high power transistors for electronic devices of medical purposes

Heuristic Model of Forecasting of Operating State of Semiconductor Devices

The reason for a high Ca2+-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycle

The primary cause of muscle disfunction associated with substitutions E240K and R244G in tropomyosin is aberrant behavior of tropomyosin and response of actin and myosin during ATPase cycle

Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle

Accelerated Testing of High Power Transistors for Long Operation when Solving Problems of Prediction of their Reliability by the Method of Imitation Simulation

Hard- and software simulation tools of emergency control system of turbine frequency and power regulators

The reason for the low Ca2+-sensitivity of thin filaments associated with the Glu41Lys mutation in the TPM2 gene is “freezing” of tropomyosin near the outer domain of actin and inhibition of actin monomer switching off during the ATPase cycle

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