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  1. 1
    Academic Journal

    Contributors: The study was financially supported by the Russian Science Foundation and the Perm Territory as part of a research project № 22-25-20121., Исследование выполнено при финансовой поддержке РНФ и Пермского края в рамках научного проекта № 22-25-20121.

    Source: Medical Immunology (Russia); Том 25, № 3 (2023); 465-468 ; Медицинская иммунология; Том 25, № 3 (2023); 465-468 ; 2313-741X ; 1563-0625

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    Relation: https://www.mimmun.ru/mimmun/article/view/2798/1665; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/11749; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/11750; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/11751; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/11752; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/11753; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/12212; https://www.mimmun.ru/mimmun/article/downloadSuppFile/2798/12213; Calamini B., Santarsiero B.D., Boutin J.A., Mesecar A.D. Kinetic, thermodynamic and X-ray structural insights into the interaction of melatonin and analogues with quinone reductase 2. Biochem. J., 2008, Vol. 413, no. 1, pp. 81-91.; Carrillo-Vico A., Lardone P.J., Naji L., Fernandez-Santos J.M., Martin-Lacave I., Guerrero J.M., Calvo J.R. Beneficial pleiotropic actions of melatonin in an experimental model of septic shock in mice: Regulation of pro-/ anti-inflammatory cytokine network, protection against oxidative damage and anti-apoptotic effects. J. Pineal. Res., 2005, Vol. 39, pp. 400-408.; Espino J., Rodriguez A.B., Pariente J.A. The inhibition of TNF-α-induced leucocyte apoptosis by melatonin involves membrane receptor MT1/MT2 interaction. J. Pineal. Res., 2013, Vol. 54, no. 4, pp. 442- 452.; Farez M.F., Mascanfroni I.D., Mendez-Huergo S.P., Yeste A., Murugaiyan G., Garo L.P., Balbuena Aguirre M.E., Patel B., Ysrraelit M.C., Zhu C., Kuchroo V.K., Rabinovich G.A., Quintana F.J., Correale J. Melatonin Contributes to the Seasonality of Multiple Sclerosis Relapses. Cell, 2015, Vol. 162, pp. 1338-1352.; Ferlazzo N., Andolina G., Cannata A., Costanzo M.G., Rizzo V., Curro M., Ientile R., Caccamo D. Is Melatonin the Cornucopia of the 21st Century? Antioxidants, 2020, Vol. 9, no. 11, 1088. doi:10.3390/antiox9111088.; Garcia-Maurino S., Gonzalez-Haba M.G., Calvo J.R., Rafii-El-Idrissi M., Sanchez-Margalet V., Goberna R., Guerrero J.M. Melatonin enhances IL-2, IL-6, and IFNγ production by human circulating CD4+ cells: a possible nuclear receptor-mediated mechanism involving T helper type 1 lymphocytes and monocytes. J. Immunol., 1997, Vol. 159, pp. 574-581.; Glebezdina N.S., Olina A.A., Nekrasova I.V., Kuklina E.M. Molecular Mechanisms of control of differentiation of regulatory T-lymphocytes by exogenous melatonin. Dokl. Biochem. Biophys., 2019, Vol. 484, no. 1, pp. 13-16.; Gupta S., Haldar C. Physiological crosstalk between melatonin and glucocorticoid receptor modulates t-cell mediated immune responses in a wild tropical rodent, funambulus pennant. J. Steroid. Biochem. Mol. Biol., 2013, Vol. 134, pp. 23-36.; Kuklina E.M., Glebezdina N.S., Nekrasova I.V. Role of melatonin in the regulation of differentiation of T cells producing interleukin-17 (Th17). Bull. Exp. Biol. Med., 2016, Vol. 160, no. 5, pp. 656-658.; Lardone P.J., Rubio A., Cerrillo I., Gomez-Corvera A., Carrillo-Vico A., Sanchez-Hidalgo M., Guerrero J.M., Fernandez-Riejos P., Sanchez-Margalet V., Molinero P. Blocking of melatonin synthesis and MT(1) receptor impairs the activation of Jurkat T cells. Cell. Mol. Life. Sci., 2010, Vol. 67, pp. 3163-3172.; Lardone P.J., Guerrero J.M., Fernandez-Santos J.M., Rubio A., Martin-Lacave I., Carrillo-Vico A. Melatonin synthesized by T lymphocytes as a ligand of the retinoic acid-related orphan receptor. J. Pineal Res., 2011, Vol. 51, pp. 454-462.; Naranjo M.C., Guerrero J.M., Rubio A., Lardone P.J., Carrillo-Vico A., Carrascosa-Salmoral M.P., Jimenez-Jorge S., Arellano M.V., Leal-Noval S.R., Leal M., Lissen E., Molinero P. Melatonin biosynthesis in the thymus of humans and rats. Cell. Mol. Life Sci., 2007, Vol. 64, no. 6, pp. 781-790.; Ragonda F., Diederich M., Ghibelli L. Melatonin: a pleiotropic molecule regulating inflammation. Biochem. Pharmacol., 2010, Vol. 80, pp. 1844-1852.; Raghavendra V., Singh V., Shaji A.V., Vohra H., Kulkarni S.K., Agrewala J.N. Melatonin provides signal 3 to unprimed CD4(+) T cells but failed to stimulate LPS primed B cells. Clin. Exp. Immunol., 2001, Vol. 124, pp. 414-422.; Reppert S.M., Weaver D.R., Ebisawa T. Cloning and characterization of a mammalian melatonin receptor that mediates reproductive and circadian responses. Neuron, 1994, Vol. 13, no. 5, pp. 1177-1185; https://www.mimmun.ru/mimmun/article/view/2798

  2. 2
    Academic Journal

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    Relation: Vlasova K. V. Circadian dynamics of optic density of melatonin receptors in the neurons of hypothalamic supraoptic nucleus in rats under altered photoperiod / K. V. Vlasova, R. Ye. Bulyk // Актуальні проблеми сучасної медицини: Вісник Української медичної стоматологічної академії. – 2019. – Т. 19, вип. 3 (63). – С. 117–120.; https://repository.pdmu.edu.ua/handle/123456789/12608

  3. 3
    Academic Journal

    Source: Клінічна анатомія та оперативна хірургія; Том 14, № 4 (2015): Клінічна анатомія та оперативна хірургія; 91-94
    Клиническая анатомия и оперативная хирургия; Том 14, № 4 (2015): Клиническая анатомия и оперативная хирургия; 91-94
    Clinical anatomy and operative surgery; Том 14, № 4 (2015): Clinical Anatomy and Operative Surgery; 91-94

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