Zobrazeno 1 - 6
of 6
pro vyhledávání: '"E. N. Suspitsyn"'
Autor:
G. A. Janus, A. G. Ievleva, E. N. Suspitsyn, V. I. Tyurin, I. V. Bizin, O. A. Gorustovich, V. I. Ni, M. M. Kholmatov, T. A. Laidus, S. A. Chuynyshena, S. N. Aleksakhina, E. N. Imyanitov
Publikováno v:
Сибирский онкологический журнал, Vol 19, Iss 4, Pp 123-131 (2020)
Despite the unprecedented success in using immune checkpoint inhibitors in the treatment of lung cancer, melanoma, hypermutable tumors of various localization, etc., a significant proportion of patients receiving these drugs do not respond to treatme
Externí odkaz:
https://doaj.org/article/c3a2800fe9394defaa9436a7283d7c1b
Publikováno v:
Современная ревматология, Vol 14, Iss 1, Pp 101-107 (2020)
The paper presents data on the pathogenesis of systemic lupus erythematosus (SLE), and depicts various molecular mechanisms for the development of SLE and lupus-like syndromes. It describes groups of diseases, such as apoptotic defects; NETosis; inte
Externí odkaz:
https://doaj.org/article/fb3533fafc9242f4b06b90e53f2e3b55
Autor:
M. F. Dubko, E. N. Suspitsyn, A. P. Sokolenko, E. N. Imyanitov, T. S. Likhacheva, A. Yu. Kazantseva, O. V. Kalashnikova, V. G. Chasnyk, M. M. Kostik
Publikováno v:
Современная ревматология, Vol 11, Iss 2, Pp 41-46 (2017)
Autoinflammatory diseases (AIDs) are a group of rare disorders characterized by persistent or recurrent inflammation caused by the hyperactivation of mediators and innate immune cells (neutrophils, monocytes/macrophages). The paper describes the auth
Externí odkaz:
https://doaj.org/article/34711b88ab69439c8db9e3f8ba5d9e19
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 62, Iss 3, Pp 79-84 (2017)
The article presents literature data and a clinical case on the rare Imerslund-Grasbeck syndrome. The pathogenetic foundations, the features of the clinical picture, course and treatment of this syndrome in children are discussed. Own clinical observ
Publikováno v:
Voprosy onkologii. 62(6)
Whole exome sequencing (WES) has become a leading tool for genetic analysis right after its invention. This approach permits the detection of mutations spread within coding regions of the entire genome. For cancer patients WES is particularly effecti
Autor:
L M, Bershteĭn, E N, Imianitov, E N, Suspitsyn, M Iu, Grigor'ev, E P, Sokolov, A V, Togo, K P, Khanson, T E, Poroshina, V B, Gamaiunova, D A, Vasil'ev, A Iu, Kovalevskiĭ, O N, Volkov
Publikováno v:
Voprosy onkologii. 46(3)
A strong connection is known to exist between initiation/promotion of endometrial cancer and excess of estrogens. Therefore, participation of certain alleles of genetic polymorphisms in steroid biosynthesis or metabolism may be responsible for predis