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Khusainova, Rita (2022) by marked
polymorphism with variable severity of skeletal and extra-skeletal features. Previous studies have
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gene demonstrated that CC genotype and C allele carriers had higher risk of developing
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Zaplakhova, OV,
Bakhtiiarova, KZ (2022) : We demonstrate the association with multiple sclerosis of the five
variants (INAVA rs7522462, EOMES
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Khusnutdinova, E. (2022) hormones, and drugs, including those used in COVID-19 treatment. Cytochrome
p450
genes are linked
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Viktorov, V.V.,
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Викторов, В.В. (2022) Correlations of
Gene Variants LEP rs2167270, LEPR rs1137100, GHRL rs696217, rs27647, and NPY rs
Dobrodeeva, V.S.,
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Nasyrova, R.F. (2022) and proopiomelanocortin receptors. We studied the association of the single-nucleotide
variants (SNVs) rs11100494 and rs
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Khusnutdinova, E. (2022) variants, located in microRNA biogenesis
genes, in 464 individuals with clinically diagnosed ccRCC and 1042
genes, HLA
genes and in the anti-inflammatory cytokine (IL-4)
gene,
polymorphisms in phospholipase