Search Results - "Slominsky, Petr A."

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    Genetics Factors in Major Depression Disease by Shadrina, Maria, Bondarenko, Elena A, Slominsky, Petr A

    Published in Frontiers in psychiatry (23-07-2018)
    “…Depressive disorders (DDs) are one of the most widespread forms of psychiatric pathology. According to the World Health Organization, about 350 million people…”
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    Genetic Architecture of Parkinson’s Disease by Shadrina, Maria I., Slominsky, Petr A.

    Published in Biochemistry (Moscow) (01-03-2023)
    “…Year 2022 marks 25 years since the first mutation in familial autosomal dominant Parkinson’s disease was identified. Over the years, our understanding of the…”
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    Major Depression: One Brain, One Disease, One Set of Intertwined Processes by Filatova, Elena V., Shadrina, Maria I., Slominsky, Petr A.

    Published in Cells (Basel, Switzerland) (21-05-2021)
    “…Major depressive disorder (MDD) is a heterogeneous disease affecting one out of five individuals and is the leading cause of disability worldwide. Presently,…”
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    Whole Transcriptome Analysis of Substantia Nigra in Mice with MPTP-Induced Parkinsonism Bearing Defective Glucocerebrosidase Activity by Usenko, Tatiana, Bezrukova, Anastasia, Rudenok, Margarita M, Basharova, Katerina, Shadrina, Maria I, Slominsky, Petr A, Zakharova, Ekaterina, Pchelina, Sofya

    “…Mutations in the gene represent the major genetic risk factor for Parkinson's disease (PD). The lysosomal enzyme beta-glucocerebrosidase (GCase) encoded by the…”
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    Maternal Methyl-Enriched Diet Increases DNMT1, HCN1, and TH Gene Expression and Suppresses Absence Seizures and Comorbid Depression in Offspring of WAG/Rij Rats by Sarkisova, Karine Yu, Fedosova, Ekaterina A, Shatskova, Alla B, Rudenok, Margarita M, Stanishevskaya, Vera A, Slominsky, Petr A

    Published in Diagnostics (Basel) (21-01-2023)
    “…The reduced expression of the HCN1 ion channel in the somatosensory cortex (SSC) and mesolimbic dopamine deficiency are thought to be associated with the…”
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    Housekeeping Genes for Parkinson’s Disease in Humans and Mice by Alieva, Anelya Kh, Filatova, Elena V., Rudenok, Margarita M., Slominsky, Petr A., Shadrina, Maria I.

    Published in Cells (Basel, Switzerland) (30-08-2021)
    “…A critical aspect of real-time PCR is the presence of housekeeping genes (HKGs) as an internal control for the normalization of expression data for genes of…”
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    Transcriptome Profiling Reveals Differential Expression of Circadian Behavior Genes in Peripheral Blood of Monozygotic Twins Discordant for Parkinson's Disease by Semenova, Ekaterina I, Vlasov, Ivan N, Partevian, Suzanna A, Rosinskaya, Anna V, Rybolovlev, Ivan N, Slominsky, Petr A, Shadrina, Maria I, Alieva, Anelya Kh

    Published in Cells (Basel, Switzerland) (01-08-2022)
    “…Parkinson's disease (PD) is one of the most common neurodegenerative diseases. Investigating individuals with the most identical genetic background is optimal…”
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    Expression Analysis of Genes Involved in Transport Processes in Mice with MPTP-Induced Model of Parkinson's Disease by Rudenok, Margarita M, Shadrina, Maria I, Filatova, Elena V, Rybolovlev, Ivan N, Nesterov, Maxim S, Abaimov, Denis A, Ageldinov, Ruslan A, Kolacheva, Anna A, Ugrumov, Michael V, Slominsky, Petr A, Alieva, Anelya Kh

    Published in Life (Basel, Switzerland) (19-05-2022)
    “…Processes of intracellular and extracellular transport play one of the most important roles in the functioning of cells. Changes to transport mechanisms in a…”
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    Targeted exome analysis of Russian patients with hypertrophic cardiomyopathy by Filatova, Elena V., Krylova, Natalia S., Vlasov, Ivan N., Maslova, Maria S., Poteshkina, Natalia G., Slominsky, Petr A., Shadrina, Maria I.

    Published in Molecular genetics & genomic medicine (01-11-2021)
    “…Background Hypertrophic cardiomyopathy (HCM), described as the presence of hypertrophy of left ventricular, is the most prevalent heritable cardiovascular…”
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    Potential Biomarkers of the Earliest Clinical Stages of Parkinson's Disease by Slominsky, Petr A., Illarioshkin, Sergey N., Karabanov, Aleksey V., Filatova, Elena V., Alieva, Anelya Kh, Shadrina, Maria I.

    Published in Parkinson's disease (01-01-2015)
    “…Parkinson’s disease (PD) is a widespread neurodegenerative disorder. Despite the intensive studies of this pathology, in general, the picture of the…”
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    GSTM1 copy number variation in the context of single nucleotide polymorphisms in the human GSTM cluster by Khrunin, Andrey V, Filippova, Irina N, Aliev, Aydar M, Tupitsina, Tat'yana V, Slominsky, Petr A, Limborska, Svetlana A

    Published in Molecular cytogenetics (19-04-2016)
    “…GSTM1 gene deletion is one of the most known copy number polymorphisms in human genome. It is most likely caused by homologous recombination between the…”
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    miRNA expression is highly sensitive to a drug therapy in Parkinson's disease by Alieva, Anelya Kh, Filatova, Elena V, Karabanov, Aleksey V, Illarioshkin, Sergey N, Limborska, Svetlana A, Shadrina, Maria I, Slominsky, Petr A

    Published in Parkinsonism & related disorders (01-01-2015)
    “…Abstract Background miRNAs may play a role in the pathogenesis of Parkinson's disease. It is necessary to continue the search for new miRNAs that may affect…”
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    A new digital approach to SNP encoding for DNA identification by Garafutdinov, Ravil R., Sakhabutdinova, Assol R., Slominsky, Petr A., Aminev, Farit G., Chemeris, Alexey V.

    Published in Forensic science international (01-12-2020)
    “…•SNP data are digitized as whole 4-bit boxes in the most convenient binary format.•Digitization of SNP data enables creating unique genetic identification…”
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    Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage by Shadrina, Maria I, Semenova, Elena V, Slominsky, Petr A, Bagyeva, Gulbahar H, Illarioshkin, Sergei N, Ivanova-Smolenskaia, Irina I, Limborska, Svetlana A

    Published in BMC medical genetics (26-02-2007)
    “…One of the causes of Parkinson's disease is mutations in the PARK2 gene. Deletions and duplications of single exons or exon groups account for a large…”
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    Transcriptome Profile Changes in Mice with MPTP-Induced Early Stages of Parkinson’s Disease by Alieva, Anelya Kh, Filatova, Elena V., Kolacheva, Anna A., Rudenok, Margarita M., Slominsky, Petr A., Ugrumov, Mikhail V., Shadrina, Maria I.

    Published in Molecular neurobiology (01-11-2017)
    “…Parkinson’s disease (PD) is one of the most common neurodegenerative diseases. Despite progress in the study of the molecular, genetic, and pathogenic…”
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