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ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia

Cerebellum & ataxias, 2016-01, Vol.3 (1), p.2-2, Article 2

2016

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Expression analysis of genes of ubiquitin-proteasome protein degradation system in MPTP-induced mice models of early stages of Parkinson’s disease

Doklady. Biochemistry and biophysics, 2014-05, Vol.456 (1), p.116-118

2014

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Prospects for the Use of Cell Cultures in Modeling Myocardial Diseases: Hypertrophic Cardiomyopathy

Cell and tissue biology, 2024, Vol.18 (4), p.360-379

2024

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Whole-Transcriptome Analysis of Mouse Models with MPTP-Induced Early Stages of Parkinson’s Disease Reveals Stage-Specific Response of Transcriptome and a Possible Role of Myelin-Linked Genes in Neurodegeneration

Molecular neurobiology, 2018-09, Vol.55 (9), p.7229-7241

2018

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Reference Genes for the Real-Time PCR Analysis of Relative Gene Expression in Various Human Myocardial Pathologies

Nanobiotechnology Reports (Online), 2024, Vol.19 (3), p.432-436

2024

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Screening and Stability Analysis of Housekeeping Genes for Transcriptomic Studies in Danio rerio (Zebrafish) at Early Developmental Stages

Molecular genetics, microbiology and virology, 2024, Vol.39 (2), p.131-136

2024

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Rare Mutations V453X and Y847X in the MYBPC3 Gene Do Not Lead to a Severe Form of Hypertrophic Cardiomyopathy in the Russian Population

Molecular genetics, microbiology and virology, 2023-12, Vol.38 (4), p.222-225

2023

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The Effect of Morpholino Oligonucleotides to Gene Anxa2a on the Embryonic Development of Danio rerio

Molecular genetics, microbiology and virology, 2023-09, Vol.38 (3), p.143-149

2023

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Expression analysis of genes involved in mitochondrial biogenesis in mice with MPTP-induced model of Parkinson's disease

Molecular genetics and metabolism reports, 2020-06, Vol.23, p.100584-100584, Article 100584

2020

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No Effect of the p.Arg230His Variant Of The VCL Protein on the Course of the Hypertrophic Cardiomyopathy In Russian Family Carrying The p.Gln1233Ter Pathogenic Variant In The MYBPC3 Gene

Kardiologiia, 2023-03, Vol.63 (3), p.28-35

2023

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MicroRNAs: Possible role in pathogenesis of Parkinson’s disease

Biochemistry (Moscow), 2012-08, Vol.77 (8), p.813-819

2012

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Prevalence of MYBPC3 Gene Mutations in Russian Patients with Hypertrophic Cardiomyopathy

Molecular genetics, microbiology and virology, 2023-03, Vol.38 (1), p.16-20

2023

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Protein p53 Expression and Dark Neurons in Rat Hippocampus after Experimental Septoplasty Simulation

Molecular genetics, microbiology and virology, 2022-03, Vol.37 (1), p.19-24

2022

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Peptide Pharmaceuticals: Opportunities, Prospects, and Limitations

Molecular genetics, microbiology and virology, 2018, Vol.33 (1), p.8-14

2018

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Relative Levels of DNM2, EPN2, and EXOC4 Gene Expression in Peripheral Blood of Parkinson’s Disease Patients

Molecular genetics, microbiology and virology, 2021-07, Vol.36 (3), p.139-143

2021

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Molecular Mechanisms of Pathogenesis of Parkinson's Disease

International Review of Cell and Molecular Biology, 2010, Vol.281, p.229-266

2010

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Mitochondrial dysfunction and oxidative damage in the molecular pathology of Parkinson's disease

Molecular biology (New York), 2008-10, Vol.42 (5), p.720-728

2008

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The Frequency of Heterozygous Carriage of the PAH Gene Nucleotide Sequence Variants Associated with the Development of Phenylketonuria in the ESSE-Vologda Population-Based Cohort Study

Molecular genetics, microbiology and virology, 2021-04, Vol.36 (2), p.92-99

2021

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Analysis of Expression of Genes CLN3, GABBR1, and WFS1 in Patients with Parkinson’s Disease

Molecular genetics, microbiology and virology, 2020-04, Vol.35 (2), p.85-89

2020

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Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy

Brain (London, England : 1878), 1996-12, Vol.119 (6), p.1895-1909

1996

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Phosphodiesterase 4D (PDE4D) gene polymorphism in patients with acute stroke from Moscow

Russian journal of genetics, 2010-06, Vol.46 (6), p.765-768

2010

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Possible involvement of neuronal nicotinic acetylcholine receptors in compensatory brain mechanisms at early stages of Parkinson's disease

Biomeditsinskaia khimiia, 2017-05, Vol.63 (3), p.241-247

2017

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Associations between chronotype, road accidents and polymorphisms in genes linked with biological clock and dopaminergic system

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2017, Vol.117 (4. Vyp. 2), p.28

2017

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The association of hemostasis system genes with the development of ischemic stroke in patients under the age of 50 years

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2018, Vol.118 (9. Vyp. 2), p.14

2018

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An Association Study of rs10462021 Polymorphism in the Clock Gene PERIOD3 and Different Clinical Types of Depression

Molecular genetics, microbiology and virology, 2018, Vol.33 (1), p.26-29

2018

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ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia

Expression analysis of genes of ubiquitin-proteasome protein degradation system in MPTP-induced mice models of early stages of Parkinson’s disease

Prospects for the Use of Cell Cultures in Modeling Myocardial Diseases: Hypertrophic Cardiomyopathy

Whole-Transcriptome Analysis of Mouse Models with MPTP-Induced Early Stages of Parkinson’s Disease Reveals Stage-Specific Response of Transcriptome and a Possible Role of Myelin-Linked Genes in Neurodegeneration

Reference Genes for the Real-Time PCR Analysis of Relative Gene Expression in Various Human Myocardial Pathologies

Screening and Stability Analysis of Housekeeping Genes for Transcriptomic Studies in Danio rerio (Zebrafish) at Early Developmental Stages

Rare Mutations V453X and Y847X in the MYBPC3 Gene Do Not Lead to a Severe Form of Hypertrophic Cardiomyopathy in the Russian Population

The Effect of Morpholino Oligonucleotides to Gene Anxa2a on the Embryonic Development of Danio rerio

Expression analysis of genes involved in mitochondrial biogenesis in mice with MPTP-induced model of Parkinson's disease

No Effect of the p.Arg230His Variant Of The VCL Protein on the Course of the Hypertrophic Cardiomyopathy In Russian Family Carrying The p.Gln1233Ter Pathogenic Variant In The MYBPC3 Gene

MicroRNAs: Possible role in pathogenesis of Parkinson’s disease

Prevalence of MYBPC3 Gene Mutations in Russian Patients with Hypertrophic Cardiomyopathy

Protein p53 Expression and Dark Neurons in Rat Hippocampus after Experimental Septoplasty Simulation

Peptide Pharmaceuticals: Opportunities, Prospects, and Limitations

Relative Levels of DNM2, EPN2, and EXOC4 Gene Expression in Peripheral Blood of Parkinson’s Disease Patients

Molecular Mechanisms of Pathogenesis of Parkinson's Disease

Mitochondrial dysfunction and oxidative damage in the molecular pathology of Parkinson's disease

The Frequency of Heterozygous Carriage of the PAH Gene Nucleotide Sequence Variants Associated with the Development of Phenylketonuria in the ESSE-Vologda Population-Based Cohort Study

Analysis of Expression of Genes CLN3, GABBR1, and WFS1 in Patients with Parkinson’s Disease

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy

Phosphodiesterase 4D (PDE4D) gene polymorphism in patients with acute stroke from Moscow

Possible involvement of neuronal nicotinic acetylcholine receptors in compensatory brain mechanisms at early stages of Parkinson's disease

Associations between chronotype, road accidents and polymorphisms in genes linked with biological clock and dopaminergic system

The association of hemostasis system genes with the development of ischemic stroke in patients under the age of 50 years

An Association Study of rs10462021 Polymorphism in the Clock Gene PERIOD3 and Different Clinical Types of Depression

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