Savelieva, O.N.,
Karunas, A.S.,
Vlasova, A.O.,
Ahmetshin, A.A.,
Khidiyatova, I.M.,
Khusnutdinova, E.K. (2024) Asthma is a common chronic multifactorial respiratory disease.
Genes involved in the metabolism
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
1800544, rs553668)
genes to estimate their effect on quantitative parameters, including glucose, insulin
Ivanov, A.M.,
Gil'manov, A.Z.,
Malyutina, N.N.,
Khovaeva, Y.B.,
Nenasheva, O.Y.,
El'kin, G.I.,
Sosnin, D.Y. (2020) was to estimate frequency of genetic polymorphisms (SNP) in folate cycle
genes among people living in Perm region
of neurotransmitter
genes can impact eating behavior. The aim of this study was to detect the associations between
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
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
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
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
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