of information. Results and discussion Mutations in proinflammatory cytokine and receptor
genes, metalloprotease
», «treatment», «frequency», «prevalence», «genotype-phenotype correlation», « modifier
genes». Results
by specific mutations in the NF1
gene (causing substitutions of amino acids in neurofibromin: p.Arg1038, p
of polymorphic variants of inflammation
genes with MetS and serum levels of high-sensitivity C-reactive protein
Dobrodeeva, V.S.,
Shnayder, N.A.,
Novitsky, M.A.,
Asadullin, A.R.,
Vaiman, E.E.,
Petrova, M.M.,
Limankin, O.V.,
Neznanov, N.G.,
Garganeeva, N.P.,
Nasyrova, R.F. (2022) 6837793 of the NPY5R
gene, and rs16147, rs5573, rs5574 of the NPY
gene, with metabolic disorders
Dzhaubermezov, M.,
Ekomasova, N.,
Mustafin, R.,
Gabidullina, L.,
Galimova, Y.,
Nurgalieva, A.,
Valova, Y.,
Prokofyeva, D.,
Khusnutdinova, E. (2022) hormones, and drugs, including those used in COVID-19 treatment. Cytochrome
p450
genes are linked
Kochetova, O. V.,
Shangareeva, Z.A.,
Viktorova, T.V.,
Korytina, G.F.,
Viktorov, V.V.,
Кочетова, О.В.,
Шангареева, З.А.,
Викторова, Т.В.,
Корытина, Г.Ф.,
Викторов, В.В. (2022) Correlations of
Gene Variants LEP rs2167270, LEPR rs1137100, GHRL rs696217, rs27647, and NPY rs