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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
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)
, ALDH7A1, ADCYAP1, HNMT, PSAP, and SCG3 genes involved in the histamine metabolism in the development
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
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
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
ГЕННАЯ ТЕРАПИЯ: РИСКИ И ПРЕИМУЩЕСТВА
GENE THERAPIES: RISK AND BENEFITS
Янбердина, К.И., Сад, А.С., Yanberdina, K.I., Sad, A.S. (2024)
GENE THERAPIES: RISK AND BENEFITS
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
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
INVESTIGATION OF THE ROLE OF CYTOKINE GENES POLYMORPHISMS IN THE DEVELOPMENT OF THE URTICARIA IN THE REPUBLIC OF BASHKORTOSTAN
Gimalova, G.K., Karunas, A.S., Khusuntdinova, E.K., Khantimerova, E.F., Zagidullin, S.Z. (2017)
of interleukins genes IL4 (rs2243250), IL4R (rs1805010), IL10 (rs1800872), IL13 (rs20541) and tumor necrosis
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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