Zobrazeno 1 - 10
of 10
pro vyhledávání: '"A. V. Vagabov"'
Autor:
M. Sh. Khubutia, A. A. Temnov, A. V. Vagabov, M. P. Lebedev, A. N. Sklifas, K. A. Rogov, O. P. Fomina, O. F. Vostrikova
Publikováno v:
Трансплантология (Москва), Vol 0, Iss 4, Pp 20-25 (2018)
Data on the efficiency of low-molecular peptide preparations, selected from cultivated stem cells of marrow, in the treatment of acute kidney insufficiency in experimental animals are resulted. It is demonstrated that the use of peptide preparations
Externí odkaz:
https://doaj.org/article/018c935d47f74301966a719059febd50
Publikováno v:
Cytotherapy. 16:579-585
The purpose of this review is to systematize data from many studies and observations of proliferative, anti-apoptotic and anti-inflammatory effects of mesenchymal stromal cell (MSC) paracrine factors and their biologic effects in models of acute orga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cce5db7a67e798f21c6b6cefc569985
https://doi.org/10.1016/j.jcyt.2013.07.017
https://doi.org/10.1016/j.jcyt.2013.07.017
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1076-1080
N-methyl-2-phenylbenzotellurazolinium iodide, like other N-methylbenzochalcogenazolium salts, readily undergoes reduction, hydrolysis, and recyclization with hydrazine hydrate and o-phenylene diamine. 1-Methyl-2-phenylbenzotelluronioazole perchlorate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d41cf60149d92e723898a43841603d7e
https://doi.org/10.1007/s10593-007-0168-9
https://doi.org/10.1007/s10593-007-0168-9
Publikováno v:
Chemistry of Heterocyclic Compounds. 36:201-206
The reactions of 2-allylthiobenzimidazole, -oxazole, and-thiazole, and the thiones formed from them on heating, with dichlorocarbene have been investigated under phase transfer catalysis conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9094e07ef60c93ba99ceef9036582de7
https://doi.org/10.1007/bf02283553
https://doi.org/10.1007/bf02283553
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 109:365-368
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9e0ea727ada266ef46c976af1b8adf4
https://doi.org/10.1080/10426509608545166
https://doi.org/10.1080/10426509608545166
Publikováno v:
ChemInform. 39
N-methyl-2-phenylbenzotellurazolinium iodide, like other N-methylbenzochalcogenazolium salts, readily undergoes reduction, hydrolysis, and recyclization with hydrazine hydrate and o-phenylene diamine. 1-Methyl-2-phenylbenzotelluronioazole perchlorate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed297d7894d7c2139fb0c15c4e6ab2bf
https://doi.org/10.1002/chin.200816186
https://doi.org/10.1002/chin.200816186
Publikováno v:
ChemInform. 31
The reactions of 2-allylthiobenzimidazole, -oxazole, and-thiazole, and the thiones formed from them on heating, with dichlorocarbene have been investigated under phase transfer catalysis conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa880263a0c5f00e9cb5da8947d9e39c
https://doi.org/10.1002/chin.200049054
https://doi.org/10.1002/chin.200049054
Publikováno v:
Chemistry of Heterocyclic Compounds. 11:278-280
Alky1-2,3-dihydrobenzofurans, octahydrobenzofuran, and chromans undergo skeletal isomerization, dehydroisomerization, cis-trans isomerization, and dehydrogenation in the presence of BAU-activated charcoal. An ionic mechanism including initial strippi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::936a067fb601575078117fb94bed1a66
https://doi.org/10.1007/bf00470068
https://doi.org/10.1007/bf00470068
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b51af0b2841b10020439d2d96ba0436
https://doi.org/10.1002/chin.197605119
https://doi.org/10.1002/chin.197605119
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::224583adcc3a71e18baa9832ae960c51
https://doi.org/10.1002/chin.197527223
https://doi.org/10.1002/chin.197527223