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and controls. Determination of homocysteine levels and genetic testing of MTHFR and MTRR polymorphisms

Molecular genetic studies make it possible to determine associations of multifactorial diseases

. It is assumed that polymorphisms of the NFKB1 gene that disrupt its expression predispose to the development

ПОПУЛЯЦИОННО-ГЕНЕТИЧЕСКОЕ ИССЛЕДОВАНИЕ РАСПРЕДЕЛЕНИЯ И НАСЛЕДОВАНИЯ АЛЛЕЛЕЙ ГЕНА НЕЙРОПИЛИН-1 (NRP1) В БАШКОРТОСТАНЕPOPULATION GENETIC STUDY OF THE DISTRIBUTION AND INHERITANCE OF NEUROPILIN-1 (NRP1) GENE ALLELES

МЕТОДЫ АНАЛИЗА ДНКrestriction fragment length polymorphism

16944), MMP-1 (rs1799750) and SOD2 (rs4880) gene polymorphisms with the risk of developing vibration

in higher functions, mainly to a change in cognitive functions and perception of reality. Both genetic

polymorphic variants (SNPs). © Pleiades Publishing, Inc. 2024. ISSN 1022-7954, Russian Journal of Genetics

Abstract: The interaction of genetic, epigenetic, and environmental factors underlies

is the study of genetic markers of the disease, which have not been definitively established, due

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