Zobrazeno 1 - 6
of 6
pro vyhledávání: '"I. V. Shatalina"'
Autor:
L A. Gordeeva, O. S. Oskorbina, E. N. Voronina, E. A. Sokolova, I. V. Shatalina, R. V. Olennikova, S. L. Nersesyan, M. L. Filipenko, A. N. Glushkov
Publikováno v:
Медицинская иммунология, Vol 19, Iss 5, Pp 585-596 (2017)
Associations between IL1B (rs1143634), IL1RN (VNTR, intron 2), IL4 (VNTR, intron 3), TNFA (rs1800629, rs361525), IL6 (rs1800795), and IL10 (rs1800896) genetic polymorphisms in women with recurrent miscarriage (RM) were analyzed. We studied DNA sample
Externí odkaz:
https://doaj.org/article/727b53af10c54379bc1a0a793517dffa
ASSOCIATIONS OF POLYMORPHISMS IN CYTOKINE GENES WITH THE INFECTIOUS GENESIS Of RECCURENT MISCARRIAGE
Autor:
O. S. Popova, L. A. Gordeyeva, I. V. Shatalina, E. N. Voronina, R. V. Olennikova, S. L. Nersesyan, M. L. Filippenko, A. N. Glushkov
Publikováno v:
Acta Biomedica Scientifica, Vol 0, Iss 3(2), Pp 155-158 (2012)
The associations of polymorphisms in cytokine genes with the infectious form recurrent miscarriage were investigated. Have established, that at the women a genotype AA of a gene TNFA (rs1800629) and combination of genotypes *1/*1 genes IL1RN and GG o
Externí odkaz:
https://doaj.org/article/50ce93ee96d148ab8bf4352305a48382
Autor:
K. S. Krasilnikova, E. G. Polenok, T. P. Anosova, M. P. Anosov, L. A. Gordeyeva, O. A. Glushkova, O. S. Popova, I. V. Shatalina, M. V. Kostyanko, L. S. Raving, A. N. Glushkov
Publikováno v:
Acta Biomedica Scientifica, Vol 0, Iss 3(2), Pp 96-99 (2012)
The correlation between immune response to benzo(a)pyrene and progesterone in combination with detoxification enzyme gene polymorphism (CYPIA2*1F and GSTTI) and the occurrence of congenital malformations of the fetus was revealed. It is shown that at
Externí odkaz:
https://doaj.org/article/ae5e999521b44a0d8f1fb64e51870eee
Autor:
Elena N. Voronina, L. A. Gordeeva, I. V. Shatalina, Yu. V. Gareeva, Maksim L. Filipenko, I. M. Sutulina
Publikováno v:
Russian Journal of Genetics: Applied Research. 6:197-201
The associations of polymorphisms of the GSTM1 (del) and GSTP1 (Ile105Val) genes and smoking in a family with congenital malformations (CMs) in a newborn baby have been studied. The GSTM1 (del) and GSTP1 (Ile105Val) gene polymorphisms themselves are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a7b93f15208d537deb9534ae6d80833
https://doi.org/10.1134/s2079059716020118
https://doi.org/10.1134/s2079059716020118
Autor:
V I, Minina, Ia A, Savchenko, M L, Bakanova, A V, Ostaptseva, O S, Popova, I V, Shatalina, L V, Akin'china, V G, Druzhinin
Publikováno v:
Gigiena i sanitariia. (5)
The paper presents the results of investigating an association between the frequency of chromosome aberrations and the CYP1A1, CYP1A2*1F GSTM1, and GSTT1 genes involved in xenobiotic biotransformation in workers engaged in heat and power engineering.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8991dc3ff61f6d5d7c7eeaa880966a9
https://pubmed.ncbi.nlm.nih.gov/22184997
https://pubmed.ncbi.nlm.nih.gov/22184997
Publikováno v:
Russian Journal of Genetics: Applied Research; Mar2016, Vol. 6 Issue 2, p197-201, 5p