DSpace Collection:http://dspace.bsuedu.ru/handle/123456789/462752026-04-07T14:08:20Z2026-04-07T14:08:20ZBiological activity of mesenchymal stem cells secretome as a basis for cell-free therapeutic approachPokrovskaya, L. A.Zubareva, E. V.Nadezhdin, S. V.Lysenko, A. S.Litovkina, T. I.http://dspace.bsuedu.ru/handle/123456789/465672022-05-05T00:15:15Z2020-01-01T00:00:00ZTitle: Biological activity of mesenchymal stem cells secretome as a basis for cell-free therapeutic approach
Authors: Pokrovskaya, L. A.; Zubareva, E. V.; Nadezhdin, S. V.; Lysenko, A. S.; Litovkina, T. I.
Abstract: Therefore, the paracrine activity of conditioned medium obtained when cultivating MSCs, due to a plethora of bioactive factors, was assumed to have the most prominent cell-free therapeutic impact and can serve as a better option in the field of regenerative medicine in future2020-01-01T00:00:00ZAntiplatelet activity of new derivatives of benzimidazole containing sterically hindered phenolic group in their structureSpasov, A. A.Kucheryavenko, A. F.Gaidukova, K. A.Kosolapov, V. A.Zhukovskaya, O. N.http://dspace.bsuedu.ru/handle/123456789/465662022-05-05T00:27:34Z2020-01-01T00:00:00ZTitle: Antiplatelet activity of new derivatives of benzimidazole containing sterically hindered phenolic group in their structure
Authors: Spasov, A. A.; Kucheryavenko, A. F.; Gaidukova, K. A.; Kosolapov, V. A.; Zhukovskaya, O. N.
Abstract: The chemical class of benzimidazole derivatives with a hindered phenolic substituent in their structure is promising for the search for new antiaggregant and antioxidant drugs2020-01-01T00:00:00ZMolecular docking studies of N-substituted 4-methoxy-6-oxo-1-aryl-pyridazine-3-carboxamide derivatives as potential modulators of glutamate receptorsSeverina, H. I.Georgiyants, V. A.Kovalenko, S. M.Avdeeva, N. V.Yarcev, A. I.http://dspace.bsuedu.ru/handle/123456789/465652022-05-05T00:24:59Z2020-01-01T00:00:00ZTitle: Molecular docking studies of N-substituted 4-methoxy-6-oxo-1-aryl-pyridazine-3-carboxamide derivatives as potential modulators of glutamate receptors
Authors: Severina, H. I.; Georgiyants, V. A.; Kovalenko, S. M.; Avdeeva, N. V.; Yarcev, A. I.
Abstract: In the present study, the affinity of pyridazine derivatives for the most promising antiparkinsonian biotargets - I-III groups of metabotropic and ionotropic NMDA-glutamate receptors - was evaluated2020-01-01T00:00:00ZStudy of protective properties of butyrylcholinesterase in acute anticholinesterase poisoning on BChE-KO and BALB/c micePalikov, V. A.Palikova, Y. A.Dyachenko, I. A.http://dspace.bsuedu.ru/handle/123456789/465642022-05-05T00:24:58Z2020-01-01T00:00:00ZTitle: Study of protective properties of butyrylcholinesterase in acute anticholinesterase poisoning on BChE-KO and BALB/c mice
Authors: Palikov, V. A.; Palikova, Y. A.; Dyachenko, I. A.
Abstract: The article presents the results of studying the protective properties of recombinant human butyrylcholinesterase (rhBChE) in a model of acute anticholinesterase poisoning in mice knocked out for the BChE gene. Balb/c inbred mice were also used to demonstrate the important role of BChE2020-01-01T00:00:00Z