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genes (TNFA rs1800629, LTA rs909253, IL1B rs16944, IL2-IL21 rs
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Magzhanov, R.V. (2022) in the ATL1
gene, is one of the most common forms of HSP in European populations. Analysis of the ATL1
geneMingazheva, E.T.,
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genesYanchao, L.,
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Ahmad, A. (2022) patients, to clarify the common
genes of both, and to identify common pathways and potential drugs
ВЛИЯНИЕ ПОЛИМОРФИЗМА ГЕНА G1082AIL-10 НА ТЕЧЕНИЕ ОСТРЫХ КИШЕЧНЫХ ИНФЕКЦИЙ is played by the polymorphism of
genes responsible for the induction of the synthesis of inflammatory
Ivanova, E.,
Asadullina, D.,
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Pavlov, V.,
Khusnutdinova, E.,
Gilyazova, I. (2022) in the miRNA-146a
gene demonstrated that CC genotype and C allele carriers had higher risk of developing
Tyurin, Anton,
Merkuryeva, Elena,
Zaripova, Aliya,
Markova, Tatyana,
Nagornova, Tatyana,
Dantsev, Ilya,
Nadyrshina, Dina,
Zakharova, Ekaterina,
Khusainova, Rita (2022) shown that a mutation (c.-14C>T) in the IFITM5
gene is responsible for autosomal dominant OI type V
Gilyazova, I.R.,
Ivanova, E.A.,
Bermisheva, M.A.,
Loginova, M.V.,
Asadullina, D.D.,
Ishemgulov, R.R.,
Mustafin, A.T.,
Pavlov, V.N.,
Khusnutdinova, E.K. (2022) of polymorphic loci of the PTEN/PI3K/AKT pathway
genes rs2494750 of AKT1, rs2735343, rs2299941, rs10490920
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Bakirov, A.B.,
Mukhammadieva, G.F.,
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gene and the severity of DNA breaks.
The study revealed adverse effects produced by the chemical