Search Results - "Bryzgalov, Leonid O"
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Exploring the Genetic Predisposition to Epigenetic Changes in Alzheimer's Disease
Published in International journal of molecular sciences (27-04-2023)“…Alzheimer's disease (AD) is a prevalent type of dementia in elderly populations with a significant genetic component. The accumulating evidence suggests that…”
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A Panel of rSNPs Demonstrating Allelic Asymmetry in Both ChIP-seq and RNA-seq Data and the Search for Their Phenotypic Outcomes through Analysis of DEGs
Published in International journal of molecular sciences (06-07-2021)“…Currently, the detection of the allele asymmetry of gene expression from RNA-seq data or the transcription factor binding from ChIP-seq data is one of the…”
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Novel functional variants at the GWAS-implicated loci might confer risk to major depressive disorder, bipolar affective disorder and schizophrenia
Published in BMC neuroscience (19-04-2018)“…A challenge of understanding the mechanisms underlying cognition including neurodevelopmental and neuropsychiatric disorders is mainly given by the potential…”
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Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data
Published in PloS one (29-10-2013)“…A vast amount of SNPs derived from genome-wide association studies are represented by non-coding ones, therefore exacerbating the need for effective…”
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Novel approach to functional SNPs discovery from genome‐wide data reveals promising variants for colon cancer risk
Published in Human mutation (01-06-2018)“…In the majority of colorectal cancer (CRC) cases, the genetic basis of predisposition remains unexplained. The goal of the study was to assess the regulatory…”
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Potentialities of aberrantly methylated circulating DNA for diagnostics and post-treatment follow-up of lung cancer patients
Published in Lung cancer (Amsterdam, Netherlands) (01-09-2013)“…Abstract To date, aberrant DNA methylation has been shown to be one of the most common and early causes of malignant cell transformation and tumors of…”
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Application of quantitative trait locus mapping and transcriptomics to studies of the senescence-accelerated phenotype in rats
Published in BMC genomics (19-12-2014)“…Etiology of complex disorders, such as cataract and neurodegenerative diseases including age-related macular degeneration (AMD), remains poorly understood due…”
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Regulatory single nucleotide polymorphisms at the beginning of intron 2 of the human KRAS gene
Published in Journal of biosciences (01-12-2015)“…There are two regulatory single nucleotide polymorphisms (rSNPs) at the beginning of the second intron of the mouse K-ras gene that are strongly associated…”
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Species-specific effects of the hepatocarcinogens 3′-methyl-4-dimethyl-aminoazobenzene and ortho-aminoazotoluene in mouse and rat liver
Published in Molecular carcinogenesis (01-12-2005)“…The effects of rat‐specific hepatocarcinogen 3′‐methyl‐4‐dimethylaminoazobenzene (3′‐MeDAB), mouse‐specific hepatocarcinogen ortho‐aminoazotoluene (OAT),…”
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Regulatory single nucleotide polymorphisms (rSNPs) at the promoters 1A and 1B of the human APC gene
Published in BMC genetics (22-12-2016)“…Germline mutations in the coding sequence of the tumour suppressor APC gene give rise to familial adenomatous polyposis (which leads to colorectal cancer) and…”
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Regulatory single nucleotide polymorphisms
Published in BMC genetics (22-12-2016)“…Germline mutations in the coding sequence of the tumour suppressor APC gene give rise to familial adenomatous polyposis (which leads to colorectal cancer) and…”
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