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Institution

I.M. Sechenov First Moscow State Medical University

EducationMoscow, Russia
About: I.M. Sechenov First Moscow State Medical University is a education organization based out in Moscow, Russia. It is known for research contribution in the topics: Medicine & Population. The organization has 7984 authors who have published 9355 publications receiving 68997 citations.
Topics: Medicine, Population, Cancer, Disease, Blood pressure


Papers
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Journal ArticleDOI
TL;DR: Although the clinical efficacy of telepharmacy, and its cost effectiveness, are far from being fully proved, the inclusion of telePharmacy services in healthcare models may offer the unique opportunity to increase access to screening and improve care of cardiovascular conditions.

30 citations

Journal ArticleDOI
TL;DR: Thiamine compounds were able to counteract ultrasound- induced aggression, which was accompanied by the normalization of markers that have been showed to be associated with ultrasound-induced aggression.

30 citations

Journal ArticleDOI
TL;DR: Data show the importance of specific expression of Notch ligands on DCs in the regulation of T-cell effector function, and strategies incorporating selectively engineered NotCh ligands could provide a novel approach of therapeutics for modulating immunity in various immunosuppressive conditions including cancer.
Abstract: Notch intercellular communication instructs tissue-specific T-cell development and function. In this study, we explored the roles of dendritic cell (DC)-expressed Notch ligands in the regulation of T-cell effector function. We generated mice with CD11c lineage-specific deletion of Notch Delta-like ligand (Dll)1 and Jagged (Jag)2. Using these genetically-ablated mice and engineered pharmacological Notch ligand constructs, the roles of various Delta-like and Jagged ligands in the regulation of T-cell-mediated immunity were investigated. We assessed tumor growth, mouse survival, cytokine production, immunophenotyping of myeloid and lymphoid populations infiltrating the tumors, expression of checkpoint molecules and T-cell function in the experimental settings of murine lung and pancreatic tumors and cardiac allograft rejection. Correlative studies were also performed for the expression of NOTCH ligands, NOTCH receptors and PD-1 on various subsets of myeloid and lymphoid cells in tumor-infiltrating immune cells analyzed from primary human lung cancers. Mice with CD11c lineage-specific deletion of Notch ligand gene Dll1, but not Jag2, exhibited accelerated growth of lung and pancreatic tumors concomitant with decreased antigen-specific CD8+T-cell functions and effector-memory (Tem) differentiation. Increased IL-4 but decreased IFN-γ production and elevated populations of T-regulatory and myeloid-derived suppressor cells were observed in Dll1-ablated mice. Multivalent clustered DLL1-triggered Notch signaling overcame DC Dll1 deficiency and improved anti-tumor T-cell responses, whereas the pharmacological interference by monomeric soluble DLL1 construct suppressed the rejection of mouse tumors and cardiac allograft. Moreover, monomeric soluble JAG1 treatment reduced T-regulatory cells and improved anti-tumor immune responses by decreasing the expression of PD-1 on CD8+Tem cells. A significant correlation was observed between DC-expressed Jagged and Delta-like ligands with Tem-expressed PD-1 and Notch receptors, respectively, in human lung tumor-infiltrates. Our data show the importance of specific expression of Notch ligands on DCs in the regulation of T-cell effector function. Thus, strategies incorporating selectively engineered Notch ligands could provide a novel approach of therapeutics for modulating immunity in various immunosuppressive conditions including cancer.

30 citations

Journal ArticleDOI
TL;DR: In this article, four modified polymers were prepared from readily available addition poly(5-vinyl-2-norbornene) and their gas-transport properties were studied in detail.
Abstract: Herein four modified polymers were prepared from readily available addition poly(5-vinyl-2-norbornene) (PVNB) and their gas-transport properties were studied in detail. Hydrogenation, epoxidation, cyclopropanation and thiol-en reactions were chosen for the modifications of PVNB. Hydrogenation of PVNB was performed using p-toluenesulfonyl hydrazide. Epoxidation of PVNB was realized employing m-chloroperoxybenzoic acid. Cyclopropanation of PVNB was carried out using diazomethane in the presence of a Pd-catalyst. For thiol-en reaction, thioacetic acid was applied as the source of a thiol and AIBN as an initiator. All listed modifications were performed in high yields (≥80%) without the destruction of polymer main chains. The degree of functionalizations was up to 99%. The influence of these modifications on the properties of the resulting polymers was evaluated. Cyclopropanation and hydrogenation of PVNB led to an enhancement of gas permeability with minimal decrease in selectivity, while epoxidation or thioacetylation gave a substantial increase in CO2/N2 selectivity with decrease in permeability. The modified polymers with polar side-groups exhibited attractive selectivities for CO2/N2, CO2/CH4 and H2/N2 gas separations.

30 citations


Authors

Showing all 8045 results

NameH-indexPapersCitations
Yehuda Shoenfeld125162977195
Jatin P. Shah11972545680
Shahrokh F. Shariat118163758900
Vladimir P. Torchilin10962758977
Klaus-Peter Lesch10652450099
Jürgen Kurths105103862179
Rudolf Valenta10274838349
Valerian E. Kagan9766739888
Hans-Uwe Simon9646151698
Gleb B. Sukhorukov9644035549
Michael Aschner9180632826
Alexei Verkhratsky8945029788
Claudio L. Bassetti8852425332
Helgi B. Schiöth8553128628
Angelo Ravelli7941523439
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202317
2022102
20212,198
20202,343
20191,649
20181,064