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) and controls. Determination of homocysteine levels and
genetic testing of MTHFR and MTRR
polymorphismsMolecular
genetic studies make it possible to determine associations of multifactorial diseases
Nurgalieva, A.Kh.,
Mustafin, S.A.,
Petrova, S.G.,
Ekomasova, N.V.,
Sakaeva, D.D.,
Fedorova, Y.Y.,
Abdeeva, G.R.,
Dzhaubermezov, M.A.,
Abdeev, R.R.,
Rakhimov, R.R.,
Khusnutdinova, E.K.,
Prokofyeva, D.S. (2024) . It is assumed that
polymorphisms of the NFKB1 gene that disrupt its expression predispose to the development
МЕТОДЫ АНАЛИЗА ДНКrestriction fragment length
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
in higher functions, mainly to a change in cognitive functions and perception of reality. Both
genetic polymorphic variants (SNPs). © Pleiades Publishing, Inc. 2024. ISSN 1022-7954, Russian Journal of
Genetics Savelieva, O.N.,
Karunas, A.S.,
Biktasheva, A.R.,
Vlasova, A.O.,
Khidiyatova, I.M.,
Etkina, E.I.,
Khusnutdinova, E.K. (2024) Abstract: The interaction of
genetic, epigenetic, and environmental factors underlies
is the study of
genetic markers of the disease, which have not been definitively established, due