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    المصدر: Obstetrics, Gynecology and Reproduction; Vol 17, No 5 (2023); 554-564 ; Акушерство, Гинекология и Репродукция; Vol 17, No 5 (2023); 554-564 ; 2500-3194 ; 2313-7347

    وصف الملف: application/pdf

    العلاقة: https://www.gynecology.su/jour/article/view/1785/1150Test; D’Ippolito S., Tersigni C., Marana R. et al. Inflammosome in the human endometrium: further step in the evaluation of the “maternal side”. Fertil Steril. 2016;105(1):111–118.e1–4. https://doi.org/10.1016/j.fertnstert.2015.09.027Test.; Лебедева О.П., Кирко Р. Экспрессия толл-подобных рецепторов в женском репродуктивном тракте и ее гормональная регуляция (обзор). Научные результаты биомедицинских исследований. 2018;4(3):3–17.; Lebedeva O.P., Pakhomov S.P., Ivashova O.N. et al. Expression of TLR 1-10 and caspase-3 alfa in human endometrium at women with early miscarriages. Giornale Italiano di Ostetricia e Ginecologia. 2013;35(1):270–1.; Kolben T.M., Rogatsch E., Hester A. et al. Involvement of ILR4α and TLR4 in miscarriages. J Reprod Immunol. 2019;131:36–43. https://doi.org/10.1016/j.jri.2018.12.001Test.; Лебедева О.П., Жукова И.О., Ивашова О.Н. и др. Роль рецепторов RIG-I, AIM2 и IFI16. распознающих вирусную ДНК и РНК, в патогенезе самопроизвольных выкидышей и неразвивающейся беременности ранних сроков. Акушерство и гинекология. 2018;(7):57–61. https://doi.org/10.18565/aig.2018.7.57-61Test.; Лебедева О.П., Ивашова О.Н., Пахомов С.П. и др. Невынашивание беременности как проблема иммунного конфликта. Проблемы репродукции. 2014;(6):88-91.; Лебедева О.П. Роль рецепторов NOD1 и NOD2 в распознавании патогенов в женском репродуктивном тракте. Акушерство и гинекология. 2019;(5):25–9. https://doi.org/10.18565/aig.2019.5.25-29Test.; Bustin S.A., Benes V., Garson J.A. et al. The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem. 2009;55(4):611–22. https://doi.org/10.1373/clinchem.2008.112797Test.; Pffafl M.W. Quantification strategies in real-time PCR. In: AZ of quantitative PCR. Ed. S.A. Bustin. Intenational University Line, 2004. Chapter 3. 87–112. Available at: https://www.genequantification.de/chapter-3-pfaffl.pdfTest. [Accessed: 15.07.2023].; Lebedeva O.P., Popov V.N., Syromyatnikov M.Y. et al. Female reproductive tract microbiome and early miscarriages. APMIS. 2023;131(2):61–76. https://doi.org/10.1111/apm.13288Test.; Лебедева О.П., Грязнова М.В., Козаренко О.Н. и др. Микробиом влагалища при нарушениях менструального цикла (обзор). Научные результаты биомедицинских исследований. 2021;7(4):433–50. https://doi.org/10.18413/2658-6533-2021-7-4-0-9Test.; Philpott D.J., Girardin S.E. Nod-like receptors: sentinels at host membranes. Curr Opin Immunol. 2010;22(4):428–34. https://doi.org/10.1016/j.coi.2010.04.010Test; Saxena M., Yeretssian G. NOD-like receptors: master regulators of inflammation and cancer. Front Immunol. 2014;5:327. https://doi.org/10.3389/fimmu.2014.00327Test.; Lupfer C., Kanneganti T.D. Unsolved mysteries in NLR biology. Front Immunol. 2013;4:285. https://doi.org/10.3389/fimmu.2013.00285Test.; Mukherjee T., Hovingh E.S., Foerster E.G. et al. NOD1 and NOD2 in inflammation, immunity and disease. Arch Biochem Biophys. 2019;670:69–81. https://doi.org/10.1016/j.abb.2018.12.022Test.; Trindade B.C., Chen G.Y. NOD1 and NOD2 in inflammatory and infectious diseases. Immunol Rev. 2020;297(1):139–61. https://doi.org/10.1111/imr.12902Test.; King A.E., Horne A.W., Hombach-Klonisch S. et al. Differential expression and regulation of nuclear oligomerization domain proteins NOD1 and NOD2 in human endometrium: a potential role in innate immune protection and menstruation. Mol Hum Reprod. 2009;15(5):311–9. https://doi.org/10.1093/molehr/gap020Test.; Zhang Y. Chen H., Sun C. et al. Expression and functional characterization of NOD2 in decidual stromal cells Isolated during the first trimester of pregnancy. PLoS One. 2014;9(6):e99612. https://doi.org/10.1371/journal.pone.0099612Test.; Zhang Y., Yang C., Fu S. et al. Different expression of NOD2 in decidual stromal cells between normal and unexplained recurrent spontaneous abortion women during first trimester gestation. Int J Clin Exp Pathol. 2014;7(12):8784–90.; Wang Z., Liu M., Nie X. et al. NOD1 and NOD2 control the invasiveness of trophoblast cells via the MAPK/p38 signaling pathway in human first-trimester pregnancy. Placenta. 2015;36(6):652–60. https://doi.org/10.1016/j.placenta.2015.03.004Test.; Im S.S., Yousef L., Blaschitz C. et al. Linking lipid metabolism to the innate immune response in macrophages through sterol regulatory element binding protein-1a. Cell Metab. 2011;13(5):540–49. https://doi.org/10.1016/j.cmet.2011.04.001Test.; Bruey J.M., Bruey-Sedano N., Luciano F. et al. Bcl-2 and Bcl-XL regulate proinflammatory caspase-1 activation by interaction with NALP1. Cell. 2007;129(1):45–56. https://doi.org/10.1016/j.cell.2007.01.045Test.; Faustin B., Chen Y., Zhai D. et al. Mechanism of Bcl-2 and Bcl-XL inhibition of NLRP1 inflammasome: Loop domain-dependent suppression of ATP binding and oligomerization. Proc Natl Acad Sci U S A. 2009;106(10):3935–40. https://doi.org/10.1073/pnas.0809414106Test.; Lebedeva O.P., Zhukova I.O., Ivashova O.N. et al. Proteins P53 and BCL-2 in pathogenesis of missed and spontaneous abortions. Drug Invention Today. 2017;9(3):65–8.; Fusco W.G., Duncan J.A. Novel aspects of the assembly and activation of inflammasomes with focus on the NLRC4 inflammasome. Int Immunol. 2018;30(5):183–93. https://doi.org/10.1093/intimm/dxy009Test.; de Zoete M.R., Palm N.W., Zhu S. et al. Inflammasomes. Cold Spring Harb Perspect Biol. 2014;6(12):a016287. https://doi.org/10.1101/cshperspect.a016287Test.; Grasso E., Gori S., Soczewski E. et al. Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells. Sci Rep. 2018;8(1):12274. https://doi.org/10.1038/s41598-018-29779-8Test.; Lu M., Ma F., Xiao J. et al. NLRP3 inflammasome as the potential target mechanism and therapy in recurrent spontaneous abortions. Mol Med Reps. 2019;19(3):1935–41. https://doi.org/10.3892/mmr.2019.9829Test.; Denou E., Lolmède K., Garidou L. et al. Defective NOD2 peptidoglycan sensing promotes diet‐induced inflammation, dysbiosis, and insulin resistance. EMBO Mol Med. 2015;7(3):259–74. https://doi.org/10.15252/emmm.201404169Test.; Anderson B.L., Simhan H.N., Simons K.M., Wiesenfeld H.C. Untreated asymptomatic group B streptococcal bacteriuria early in pregnancy and chorioamnionitis at delivery. Am J Obstet Gynecol. 2007;196(6):524.e1–5. https://doi.org/10.1016/j.ajog.2007.01.006Test.; https://www.gynecology.su/jour/article/view/1785Test

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