Found: 7
ОБЗОР2025 · pp. 89–96
Baratova I.V., Bodunova N.A., Deeva T.A., Bordin D.S., Chebotareva M.V., Tsapkova L.A.
The aim of the study. To describe the interaction between Helicobacter pylori and Toll-like receptors, and to outline the role of TLRs gene polymorphisms in the pathogenesis of this infection. Material and methods. An analysis of publications from 2000 to 2025…
ОБЗОР2022 · pp. 3–10
Yablonsky P.K., Drobintseva A.O., Zubareva T.S., Krylova Yu.S., Leonteva D.O., Kvetnoy I.M., Paltsev M.A.
The review is devoted to the analysis of modern ideas about the molecular mechanisms of the pathogenesis of sarcoidosis, it describes the signaling molecules involved in the development of sarcoidosis, which can be biomarkers and targets for optimizing persona…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021
Ivanova А.А., Melnikova E.S., Gurazheva A.A., Malutina S.K., Rodina I.A., Khamovich O.V., Novoselov V.P., Maksimov V.N.
Introduction. Single nucleotide polymorphisms rs34643859 of the KCNS1 gene, rs12804550 of the SCN4B gene, and rs4514993 of the SCN11A gene were revealed in the analysis of the results of whole exome sequencing of a group of young man died by sudden cardiac dea…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020
Ivanova А.А., Melnikova E.S., Gurazheva A.A., Malutina S.K., Rodina I.A., Khamovich O.V., Novoselov V. P., Maksimov V.N.
Introduction. The single-nucleotide polymorphisms rs75555045 and rs12904699 were found in the own genome-wide allelotyping as possible new molecular genetic markers of sudden cardiac death (SCD). The results obtained in such studies require verification in the…
ОБЗОР2019
Dvornikova K.A., Bystrova E.Yu., Platonova O.N., Nozdrachev A.D.
Introduction. In recent years, there have been aroused and actively studied mutations associated with Toll-like receptor genes (TLRs). The emerging interest is related to the identification of many associations between the TLRs polymorphism and the development…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018
Bakhareva Yu.S., Maksimov V.N., Ivanova A.A., Chapaeva N.N.
Introduction. New technologies of DNA genotyping and sequencing contribute to the rapid accumulation of our knowledge about human genomic variations and search for inherited determinants of complex genetic traits. There is a large amount of data on association…
Research article2013
Kushlinskii N.E., Timofeev Yu.S., Generozov E.V., Naumov V.A., Soloviev Yu.N., Boulytcheva I.V.
Ethiology and pathogenesis of bone tumors presenting a rare group of oncological diseases, are not fully understood. We have studied 6 single nucleotide polymorphisms rs7921 (GH1), rs7956547(IGF1), rs3761243(GNRH2), rs11737764(FGF2), rs6599400(FGFR3), rs169091…