Zobrazeno 1 - 6
of 6
pro vyhledávání: '"E. Yu. Koldaeva"'
Autor:
A. V. Smirnova, E. Yu. Grigor’eva, Yu. V. Stukalov, V. N. Kulakov, N. S. Kalygina, E. Yu. Koldaeva, A. Yu. Baryshnikov
Publikováno v:
Pharmaceutical Chemistry Journal. 52:681-684
Targeted radioimmunotherapy is a promising approach to radiotherapy. Tumor-specific compounds were synthesized using monoclonal antibodies anti-ICO-25 (MUC1) and anti-ICO-80 (CD5) labeled with the therapeutic radioisotope 188Re. The specificity of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6958cc6d4fa6953048832b960bcae912
https://doi.org/10.1007/s11094-018-1880-8
https://doi.org/10.1007/s11094-018-1880-8
Autor:
Yu. V. Stukalov, A. S. Mas’ko, N. V. Pozdnyakova, E. Yu. Koldaeva, E. Yu. Grigor’eva, M. I. Lukashina, T. A. Sidorova
Publikováno v:
Russian Journal of Biotherapy. 16:69-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b6a4cc19174cc4c113e7fbe3ce2c41c
https://doi.org/10.17650/1726-9784-2017-16-3-69-74
https://doi.org/10.17650/1726-9784-2017-16-3-69-74
Publikováno v:
Russian Journal of Biotherapy. 15:40-43
Aim of this work was the synthesis of REDOX-dendrimer core, which is tetraglycidyl ether of pentaerythritol, and a dendron, which is a derivative of anthraquinone. Materials and methods. Analytical and preparative chromatography was carried out on a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e91961b609736111d807fdec9cedd29a
https://doi.org/10.17650/1726-9784-2016-15-4-40-43
https://doi.org/10.17650/1726-9784-2016-15-4-40-43
Autor:
N. L. Shimanovskii, N. T. Kuznetsov, K. Yu. Zhizhin, E. Yu. Koldaeva, E. L. Kadyrova, E. Yu. Grigor’eva
Publikováno v:
Pharmaceutical Chemistry Journal. 46:536-539
The influence of the chemical structure of S-containing derivatives of boron clusters intended for neutron-capture therapy (NCT) of neoplasms on the acute toxicity of these compounds was studied in mice. The toxicity characteristics depended directly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d87fb834be6ba3b7fa0a64543e291203
https://doi.org/10.1007/s11094-012-0841-x
https://doi.org/10.1007/s11094-012-0841-x
Publikováno v:
Bulletin of Experimental Biology and Medicine. 132:869-872
Mesna, an SH-containing uroprotector, attenuates the lethal effect and hematological toxicity of vepeside and taxol, but did not reduce specific activities of the studied cytostatics in mice with transplanted tumors. This selective antitoxic effect o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb784972a0641a2c8faba57641764559
https://doi.org/10.1023/a:1013126919683
https://doi.org/10.1023/a:1013126919683
Autor:
M. A. Surikova, R. A. Spryshkova, E. A. Baryshnikova, E. Yu. Koldaeva, G. I. Borisov, V. A. Sergeev, N. I. Bekasova
Publikováno v:
Pharmaceutical Chemistry Journal. 30:494-497
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31198be0ce9e5e1c01f30a335eb617eb
https://doi.org/10.1007/bf02334632
https://doi.org/10.1007/bf02334632