Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Evgeny Pislyagin"'
Autor:
Sergei Kozlovskiy, Evgeny Pislyagin, Ekaterina Menchinskaya, Ekaterina Chingizova, Yuri Sabutski, Sergey Polonik, Irina Agafonova, Dmitry Aminin
Publikováno v:
Exploration of Neuroscience, Vol 3, Iss 1, Pp 39-50 (2024)
Aim: The ability of synthetic 1,4-naphthoquinones (1,4-NQs) to prevent adenosine triphosphate (ATP)-induced and purinergic P2X7 receptor (P2X7R) mediated inflammation in macrophage and neurodegeneration of neuronal cells in vitro was previously estab
Externí odkaz:
https://doaj.org/article/094a9c866ed64e84ab0cec91174f18e1
Autor:
Wen-Han Chuang, Evgeny Pislyagin, Liang-Yu Lin, Ekaterina Menchinskaya, Oleg Chernikov, Valery Kozhemyako, Tatiana Gorpenchenko, Igor Manzhulo, Elena Chaikina, Irina Agafonova, Alexandra Silchenko, Sergey Avilov, Valentin Stonik, Shey-Cherng Tzou, Dmitry Aminin, Yun-Ming Wang
Publikováno v:
Cancer Cell International, Vol 23, Iss 1, Pp 1-17 (2023)
Abstract Background Despite intensive developments of adoptive T cell and NK cell therapies, the efficacy against solid tumors remains elusive. Our study demonstrates that macrophage-based cell therapy could be a potent therapeutic option against sol
Externí odkaz:
https://doaj.org/article/c6bbb407f8f7413c956ec9ab55bac05d
Autor:
Irina Agafonova, Ekaterina Chingizova, Elena Chaikina, Ekaterina Menchinskaya, Sergey Kozlovskiy, Galina Likhatskaya, Yuri Sabutski, Sergey Polonik, Dmitry Aminin, Evgeny Pislyagin
Publikováno v:
Marine Drugs, Vol 22, Iss 2, p 62 (2024)
The MTS cell viability test was used to screen a mini library of natural and synthetic 1,4-naphthoquinone derivatives (1,4-NQs) from marine sources. This screening identified two highly effective compounds, U-443 and U-573, which showed potential in
Externí odkaz:
https://doaj.org/article/fe7acdda1bb548a9b1836658abfa689a
Autor:
Oksana Sintsova, Irina Gladkikh, Margarita Monastyrnaya, Valentin Tabakmakher, Ekaterina Yurchenko, Ekaterina Menchinskaya, Evgeny Pislyagin, Yaroslav Andreev, Sergey Kozlov, Steve Peigneur, Jan Tytgat, Dmitry Aminin, Emma Kozlovskaya, Elena Leychenko
Publikováno v:
Biomedicines, Vol 9, Iss 3, p 283 (2021)
Kunitz-type peptides from venomous animals have been known to inhibit different proteinases and also to modulate ion channels and receptors, demonstrating analgesic, anti-inflammatory, anti-histamine and many other biological activities. At present,
Externí odkaz:
https://doaj.org/article/1e1b34edb4d842bf990c4fef7e0d9233
Autor:
Sergey Polonik, Galina Likhatskaya, Yuri Sabutski, Dmitry Pelageev, Vladimir Denisenko, Evgeny Pislyagin, Ekaterina Chingizova, Ekaterina Menchinskaya, Dmitry Aminin
Publikováno v:
Marine Drugs, Vol 18, Iss 12, p 602 (2020)
Based on 6,7-substituted 2,5,8-trihydroxy-1,4-naphtoquinones (1,4-NQs) derived from sea urchins, five new acetyl-O-glucosides of NQs were prepared. A new method of conjugation of per-O-acetylated 1-mercaptosaccharides with 2-hydroxy-1,4-NQs through a
Externí odkaz:
https://doaj.org/article/86a559cc097c42bd99214db2892359a5
Autor:
Aleksandra Kvetkina, Evgeny Pislyagin, Ekaterina Menchinskaya, Ekaterina Yurchenko, Rimma Kalina, Sergei Kozlovskiy, Leonid Kaluzhskiy, Alexander Menshov, Natalia Kim, Steve Peigneur, Jan Tytgat, Alexis Ivanov, Naira Ayvazyan, Elena Leychenko, Dmitry Aminin
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 9; Pages: 5115
Parkinson's disease (PD) is a socially significant disease, during the development of which oxidative stress and inflammation play a significant role. Here, we studied the neuroprotective effects of four Kunitz-type peptides from Heteractis crispa an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::444723847f33f71143b95303a01784f6
https://pubmed.ncbi.nlm.nih.gov/35563513
https://pubmed.ncbi.nlm.nih.gov/35563513
Autor:
Sergey, Polonik, Galina, Likhatskaya, Yuri, Sabutski, Dmitry, Pelageev, Vladimir, Denisenko, Evgeny, Pislyagin, Ekaterina, Chingizova, Ekaterina, Menchinskaya, Dmitry, Aminin
Publikováno v:
Marine Drugs
Based on 6,7-substituted 2,5,8-trihydroxy-1,4-naphtoquinones (1,4-NQs) derived from sea urchins, five new acetyl-O-glucosides of NQs were prepared. A new method of conjugation of per-O-acetylated 1-mercaptosaccharides with 2-hydroxy-1,4-NQs through a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66d4a23d15ff7bda34cc42983b74831a
https://pubmed.ncbi.nlm.nih.gov/33260299
https://pubmed.ncbi.nlm.nih.gov/33260299
Autor:
Sintsova, O. V., Chausova, V. E., Gladkikh, I. N., Isaeva, M. P., Tabakmaher, V. M., Monastyrnaya, M. M., Leychenko, E. V., Evgeny Pislyagin, Menchinskaya, E. S., Peigneur, S., Tytgat, J., Kozlovskaya, E. P.
Publikováno v:
Web of Science
ResearcherID
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1ef9ae59de3d610aa685cbd1d597ae6c
http://www.vliz.be/imisdocs/publications/292359.pdf
http://www.vliz.be/imisdocs/publications/292359.pdf
