Author

N. V. Nemchinova

2 papers indexed here

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Sep 2026

Prevalence of Polymorphic Variants rs3828942, rs144755411, rs28954118 of the Leptin Gene in Russian and Buryat Adolescents with Different Weight Status

It was shown that the frequency of the alternative allele A of rs3828942 in Buryat adolescents is significantly higher than in the group of Russian adolescents, which is consistent with global data on a higher frequency of the allele A of rs3828942 in Asian populations.

E. Belyaeva, T. Bairova, O. A. Ershova et al. · Russian Journal of Genetics · 0 citations

Open access Aug 2026

Tyrosinemia type 1: a case report

Background . Hereditary Tyrosinemia Type 1 (HT1) is an orphan disease belonging to the group of amino acid metabolism disorders, with an autosomal recessive pattern of inheritance. It is caused by a mutation in the FAH gene, which encodes the enzyme fumarylacetoacetate hydrolase. The clinical presentation is polymor...

T. Astakhova, T. Bairova, A. V. Belskikh et al. · Acta Biomedica Scientia · 0 citations