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Effect of rol Genes of the A4, 15834, and K599 Strains of Agrobacterium rhizogenes on Root Growth and States of the Antioxidant Systems of Transgenic Tobacco Plants Subjected to Abiotic Stress
Shvets, D. Yu., Berezhneva, Z.A., Musin, Kh. G., Kuluev, B.R. (2024)
An attempt is made to create transgenic plants using rol genes from A4, 15834, and K599 strains
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)
16944), MMP-1 (rs1799750) and SOD2 (rs4880) gene polymorphisms with the risk of developing vibration
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
Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases
Savelieva, O.N., Karunas, A.S., Biktasheva, A.R., Vlasova, A.O., Khidiyatova, I.M., Etkina, E.I., Khusnutdinova, E.K. (2024)
reactions. The aim of the research was to study the role of polymorphic variants of the AOC1, HRH2, HRH3
Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant
Elena, Merkuryeva, Tatiana, Markova, Anton, Tyurin, Diana, Valeeva, Vladimir, Kenis, Maria, Sumina, Igor, Sorokin, Olga, Shchagina, Mikhail, Skoblov, Maria, Nefedova, Rita, Khusainova, Ekaterina, Zakharova, Dadali, Elena, Kutsev, Sergey (2023)
with osteogenesis imperfecta. The disease is caused by pathogenic variants in the SGMS2 gene, the protein product
THE ROLE OF MTHFR AND MTRR GENE POLYMORPHISMS IN THE DEVELOPMENT OF CHOLELITHIASIS
Fedorova, Yu. Yu., Nurgalieva, A.K., Petrova, S.G., Murzina, R.R., Dzhaubermezov, M.A., Ekomasova, N.V., Khusnutdinova, E.K., Prokofieva, D.S. (2024)
)) genes with the development of gallstone disease in indi-viduals from the Republic of Bashkortostan. DNA
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
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
ROLE OF ALLELIC GENES OF MATRIX METALLOPROTEINASES AND THEIR TISSUE INHIBITORS IN THE RISK OF PEPTIC ULCER DISEASE DEVELOPMENT
Shaymardanova, E.Kh., Nurgalieva, A.Kh., Khidiyatova, I.M., Gabbasova, L.V., Kuramshina, O.A., Kryukova, A.Ya., Sagitov, R.B., Munasipov, F.R., Khusnutdinova, E.Kh. (2016)
of the stomach and/or duodenum. Association analysis of common polymorphisms of matrix metalloproteinases genes
Роль мутаций в гене NF1 в спорадическом канцерогенезе
The role of mutations in NF1 gene in sporadic carcinogenesis
Мустафин, Р. Н., Mustafin, R.N. (2021)
The review article presents data on somatic inactivation of NF1 gene as a cause of sporadic

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