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by marked polymorphism with variable severity of skeletal and extra-skeletal features. Previous studies have

in the miRNA-146a gene demonstrated that CC genotype and C allele carriers had higher risk of developing

: We demonstrate the association with multiple sclerosis of the five variants (INAVA rs7522462, EOMES

hormones, and drugs, including those used in COVID-19 treatment. Cytochrome p450 genes are linked


СПОСОБ ПРОГНОЗИРОВАНИЯ РАЗВИТИЯ ПЛОСКОСТОПИЯ У МОЛОДЫХ ЛИЦ

Correlations of Gene Variants LEP rs2167270, LEPR rs1137100, GHRL rs696217, rs27647, and NPY rs

and proopiomelanocortin receptors. We studied the association of the single-nucleotide variants (SNVs) rs11100494 and rs

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

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