Zobrazeno 1 - 9 of 9 pro vyhledávání: '"T. E. Ivaschenko"'
1
Genetic factors of predilection for habitual noncarrying of pregnancy at early stages
Autor: O. N. Bespalova, O. N. Arzhanova, T. E. Ivaschenko, M. V. Aseev, E. K. Ailamazyan, V. S. Baranov
Publikováno v: Journal of obstetrics and women's diseases. 50:8-13
By means of the method of polimerase chain reaction the frequency of blank allele of genes GSTP1, GSTM1, and the frequency of polymorphous alleles of gene GSTP1 in 40 pairs with habitual noncarrying of pregnancy at early stages were studied. The resu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::76272866bbb506dedc6c18a3e64d7c4a
https://doi.org/10.17816/jowd89431
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2
Matrix metalloproteinases’s association of polymorphisms of MMP3 and MMP9 with development of genital endometriosis
Autor: V. F. Bezhenar, V. S. Baranov, N. Yu. Shved, T. E. Ivaschenko, Arseniy S. Molotkov, M. I. Yarmolinskaya
Publikováno v: Russian Journal of Genetics. 50:205-210
We present a comparative analysis of the allelic polymorphisms of the matrix metalloproteinase (MMP) gene family, including MMP3 (rs3025058), MMP7 (rs11568818), MMP9 (rs17576, rs2250889), MMP12 (rs2276109), and MMP13 (rs2252070), in patients with ext
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b050c5b59f36076a9208aef3536c5159
https://doi.org/10.1134/s1022795414010128
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3
CFTR gene mutations in children with severe asthma
Autor: V S Tikhonova, A N Voytovich, A V Kamaev, T E Ivashchenko, A V Orlov, L A Zhelenina, D S Korostovtsev, V I Larionova, A N Voitovich, T E Ivaschenko, D S Korostovsev
Publikováno v: Russian Journal of Allergy. 8:24-27
Background. To detect sixteen cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations most common to Russian populations in children with severe asthma (SA). Patients and Methods. S A group included 59 children aged 4-17 years old (
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c8ece28d89cbe9070f01f9a145376abf
https://doi.org/10.36691/rja783
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4
Involvement of detoxification system enzymes in pathogenesis of some common multifactorial diseases. Predictive genetic testing
Autor: T. E. Ivaschenko, V. S. Baranov, E. V. Baranova
Publikováno v: Journal of obstetrics and women's diseases. 52:11-16
The review summarizes the original data concerning involvement of some genes participating in Phase I and Phase 2 of detoxification systems in the origin, progression and treatment efficiency of such common multifactorial diseases as endometriosis, b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::90d8567977ba24de636dc194a5e3ddbd
https://doi.org/10.17816/jowd88823
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5
[Untitled]
Autor: T. E. Ivaschenko, V. S. Baranov, M. A. Petrova, T. E. Gembitskaya, O. G. Sideleva, A. V. Orlov
Publikováno v: Russian Journal of Genetics. 37:94-97
The ratio between the normal (+) and null (0) alleles of the genes encoding glutatione S-transferases M1 (GSTM1) and T1 (GSTT1) were studied in normal individuals from northwestern Russia (control group) and in patients with bronchial asthma (BA). Th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::705c5a5982e3f7f825eef8d2f16b06cc
https://doi.org/10.1023/a:1009030911764
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7
Glutathione- S-transferase micro and theta gene polymorphisms as new risk factors of atopic bronchial asthma
Autor: V. S. Baranov, O G Sideleva, T. E. Ivaschenko
Publikováno v: Journal of molecular medicine (Berlin, Germany). 80(1)
The genetic polymorphism of glutathione- S-transferase M1 (GSTM1) and glutathione- S-transferase T1 (GSTT1) genes and the cytochrome P4501A1 gene responsible for xenobiotic conjugating enzymes of the phase II and phase I detoxification system were st
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e7e01cdbb4442dd6935ac90273008bb
https://pubmed.ncbi.nlm.nih.gov/11862323
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8
Five years' experience of prenatal diagnosis of cystic fibrosis in the former U.S.S.R
Autor: V. G. Vakharlovsky, A. V. Mikhailov, V. S. Baranov, V. M. Lebedev, T. K. Kascheeva, N. Yu. Shwed, V. N. Gorbunova, T. V. Kuznetzova, T. E. Ivaschenko, N. S. Osinovskaya
Publikováno v: Prenatal diagnosis. 12(7)
From a total of 490 cystic fibrosis (CF) high-risk families under supervision (mostly Russian Slavs from the European part of the country), DNA data including both direct screening for some CF gene (CFTR) mutations (delF508, G551D and 1677delTA) and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34919b9b71c0d029727d9230b8d65c40
https://pubmed.ncbi.nlm.nih.gov/1354866
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9
Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR
Autor: V. N. Gorbunova, N. Y. Shwed, V. M. Lebedev, O. P. Romanenko, V. N. Kalinin, L. A. Livshitz, A. V. Orlov, N. N. Kapranov, A. V. Mihailov, S. A. Gembovskaya, T. V. Pigina, T. E. Ivaschenko, M. T. Venozinskis, V. S. Baranov, T. E. Gembitzkaya
Publikováno v: Human genetics. 87(1)
The frequency of the F508 deletion (delta F508) has been analyzed in 189 cystic fibrosis (CF) patients from the European part of the USSR, viz. 127 northern Slavonians (Leningrad region), 30 southern Slavonians (the Ukraine), 10 central Slavonians (M
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9240b1cc95f71ce631e427c1a581e0d0
https://pubmed.ncbi.nlm.nih.gov/2037283
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