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АНАЛИЗ РАСПРОСТРАНЕНИЯ ПОЛИМОРФНОГО ВАРИАНТА rs4988235 ГЕНА MCM6 В ТЮРКОЯЗЫЧНЫХ ПОПУЛЯЦИЯХ
ANALYSIS OF THE DISTRIBUTION OF THE POLYMORPHIC VARIANT OF rs4988235 OF THE MCM6 GENE IN TURKISHSPEAKING POPULATIONS
Джаубермезов, М.А., Екомасова, Н.В., Бучнев, Д.В., Токарева, Е.А., Хуснутдинова, Э.К., Dzhaubermezov, M.A., Ekomasova, N.V., Buchnev, D.V., Tokareva, E.A., Khusnutdinova, E.K. (2020)
аллелей и генотипов полиморфного локуса rs4988235 гена MCM6 оказались статистически не значимыми.
IDENTIFICATION OF HUB GENES AND SMALL-MOLECULE COMPOUNDS RELATED TO INTRACEREBRAL HEMORRHAGE WITH BIOINFORMATICS ANALYSIS
LIU, Z., ZHANG, R., CHEN, X., YAO, P., YAN, T., LIU, W., YAO, J., ZHAO, S., SOKHATSKII, A., GAREEV, I. (2019)
obtained ten hub genes, such as IL6, TLR2, CXCL1, TIMP1, PLAUR, SERPINE1, SELE, CCL4, CCL20, and CD163
CHEMOKINE GENE POLYMORPHISMS ASSOCIATION WITH INCREASED RISK OF TYPE 2 DIABETES MELLITUS IN TATAR ETHNIC GROUP, RUSSIA
KOCHETOVA, O.V., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
revealed that some SNPs in chemokine genes are associated with obesity, insulin resistance, type 2 diabetes
THE INFLUENCE OF GENES, miRNAs AND RETROELEMENTS ON PSYCHOLOGICAL WELL-BEING
Mustafin, R.N., Khusnutdinova, E.K. (2024)
, MAOA, SLC6A3, 5-HTT genes alleles, determined by the length of VNTR in their regulatory regions
PREDICTING THE RISK OF DEVELOPING VIBRATION DISEASE AND VEGETATIVE-SENSORY POLYNEUROPATHY UNDER VIBRATION EXPOSURE USING ANALYSIS OF CANDIDATE GENE POLYMORPHISM
Mukhammadiyeva, G.F., Shaikhlislamova, E.R., Karimov, D.D., Karimov, D.O., Repina, E.F., Yakupova, T.G., Kudoyarov, E.R. (2024)
of the IL-6 gene, rs1799750 of the MMP-1 gene and rs4880 of the SOD2 gene were not found in both groups
Interaction of immune response mediator genes in a predisposition to juvenile idiopathic arthritis
Nazarova, Liliia Sh., Danilko, Ksenia V., Malievsky, Viktor A., Karimov, Denis O., Bakirov, Akhat B., Viktorova, Tatyana V. (2022)
the polymorphic loci of immune response mediator genes (TNFA rs1800629, LTA rs909253, IL1B rs16944, IL2-IL21 rs
Alu Polymorphisms of Autophagy and Apoptosis Regulatory Genes as Human Lifespan Factors
Erdman, V.V., Karimov, D.D., Tuktarova, I.A., Petintseva, A.A., Timasheva, Y.R., Nasibullin, T.R. (2025)
2, CDH4, SEMA6A, PKHD1L1, STK38L, HECW1, and TEAD1 genes, which are candidates of aging
THE ASSOCIATION BETWEEN EATING BEHAVIOR AND POLYMORPHISMS IN GRIN2B, GRIK3, GRIA1 AND GRIN1 GENES IN PEOPLE WITH TYPE 2 DIABETES MELLITUS
KOCHETOVA, O.V., KORYTINA, G.F., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2020)
of neurotransmitter genes can impact eating behavior. The aim of this study was to detect the associations between
TWO NOVEL MUTATIONS IN GENE SPG4 IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA
Akhmetgaleyevaa, A.F., Khidiyatovaa, I.M., Saifullinac, E.V., Idrisovad, R.F., Magzhanov, R.V., Khusnutdinovaa, E.K. (2016)
in Europeans is HSP associated with mutations in the spastin gene (SPG4). Analysis of the gene SPG4 was carried
Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga–Ural Region
Khidiyatova, Irina, Khidiyatova, Indira, Zinchenko, Rena, Marakhonov, Andrey, Karunas, Alexandra, Avkhadeeva, Svetlana, Aznzbaev, Marat, Khusnutdinova, Elza (2023)
and frequencies of mutations in the responsible genes, and examine clinical and genetic correlations. Based

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