Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Im, Shetova"'
Autor:
Vi, Skvortsova, Sa, Limborskaia, Im, Shetova, Petr Slominsky, Na, Shamalov, Ea, Bondarenko, Timofeev DIu
Publikováno v:
Europe PubMed Central
We studied SNP41 (rs152312) and SNP87 (rs2910829) of the PDE4D gene in 577 stroke patients and 270 healthy controls. The significant differences in the distribution of genotype and allele frequencies of the SNP41 between patients and controls were re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7fa286cefaf75a1ba5849a478d15bdef
https://pubmed.ncbi.nlm.nih.gov/23120769
https://pubmed.ncbi.nlm.nih.gov/23120769
Autor:
Tv, Tupitsyna, Ea, Bondarenko, Petr Slominsky, Im, Shetova, Na, Shamalov, Timofeev DIu, Vi, Skvortsova, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Twenty-one SNPs located in the cluster of genes FMO1-FMO2-FMO3-FMO4 and adjacent areas were analyzed in the patients with ischaemic cardioembolic stroke and in the control group. Significant differences between these samples were found in the distrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::63989d85684c726de7ec696e4fe2ccf5
https://pubmed.ncbi.nlm.nih.gov/22830265
https://pubmed.ncbi.nlm.nih.gov/22830265
Autor:
Ma, Usacheva, Tv, Nasedkina, Ikonnikova AIu, Av, Kulikov, Av, Chudinov, Lysov IuP, Ev, Bondarenko, Petr Slominsky, Na, Shamalov, Im, Shetova, Sa, Limborskaia, As, Zasedatelev, Vi, Skvortsova
Publikováno v:
Europe PubMed Central
The analysis of alleles and genotypes frequencies of 14 SNP in genes of rennin-angiotensin system (REN, AGT, AGTR1, AGTR2, BKR2, ADRB2) and hemostasis system (FGB, F2, F5, F7, ITGB3, SERPINE1, MTHFR), as well as ACE insertion-deletion polymorphism in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ec76d557ee73e164719835ccb8c27254
https://pubmed.ncbi.nlm.nih.gov/22670517
https://pubmed.ncbi.nlm.nih.gov/22670517
[Analysis association of acute ischemic stroke and DNA markers in Russian and Moldavian populations]
Autor:
Ea, Bondarenko, Im, Shetova, Na, Shamalov, Ei, Mokan, Ni, Barbakar, Gs, Kurochkin, Ss, Protopop, Lt, Lysyĭ, Petr Slominsky, Sa, Limborskaia, Vi, Skvortsova
Publikováno v:
Europe PubMed Central
Polymorphisms c.202GA of prothrombin F2 gene, c.1691GA of coagulation factor V F5 gene, c.675delinsG of plasminogen activator1 gene, and (-5)TC Kozak gene of thrombocytic receptor were studied in the Russian and Moldavian ethnic groups. We have found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ba4713c3f24be23b6f533743ffec551f
https://pubmed.ncbi.nlm.nih.gov/22232928
https://pubmed.ncbi.nlm.nih.gov/22232928
Autor:
Ea, Bondarenko, Ei, Mokan, Ni, Barbakar, Tv, Tupitsyna, Petr Slominsky, Im, Shetova, Na, Shamalov, Botsina AIu, Vi, Skvortsova, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
The risk of the ischemic stroke is mediated by both environmental and genetic factors. Recent studies of DeCode group identified the risk of polymorphisms for ischemic stroke in the phosphodiesterase 4D gene (PDE4D). The goal of this study was to exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::74c7bc06740b6f5aaf8323a4a237c7cc
https://pubmed.ncbi.nlm.nih.gov/21786629
https://pubmed.ncbi.nlm.nih.gov/21786629
Publikováno v:
Europe PubMed Central
A protein capable of activating 5-lipoxygenase (ALOX5AP) is considered a presumable risk factor of acute stroke development. Polymorphic variants of the ALOX5AP gene were examined. Two ALOX5AP gene polymorphisms (SG13S114 (rs10507391) and SG13S32 (rs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::20b21159468bdc6bba04bd1f69988fbb
https://pubmed.ncbi.nlm.nih.gov/21675249
https://pubmed.ncbi.nlm.nih.gov/21675249
Autor:
Vi, Skvortsova, Sa, Limborskaia, Im, Shetova, Petr Slominsky, Botsina AIu, Na, Shamalov, Tv, Tupitsyna
Publikováno v:
Europe PubMed Central
The role of genetic predisposition to the formation of most multifactorial diseases, including stroke, was demonstrated in a number of investigations. To determine the individual genetic risk of a polygenic disease, the candidate gene approach is use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::474a63e8a7638d560aa38121c112d4ca
https://pubmed.ncbi.nlm.nih.gov/20879099
https://pubmed.ncbi.nlm.nih.gov/20879099
Autor:
Ea, Bondarenko, Tv, Tupitsyna, Petr Slominsky, Im, Shetova, Na, Shamalov, Botsina AIu, Vi, Skvortsova, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Two PDE4D gene polymorphisms [SNP41 (rs152312 and SNP87 (rs 2910829)] were studied in patients with acute stroke (n = 577) and in control sample (n = 270). Significant differences in the genotype and allele frequency distribution were found between t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1e2bd18a8c45336b01ede4680855b59a
https://pubmed.ncbi.nlm.nih.gov/20734779
https://pubmed.ncbi.nlm.nih.gov/20734779
Autor:
Vi, Skvortsova, Petr Slominsky, Lv, Gubskii, Ea, Koltsova, Im, Shetova, Ia, Platonova, Ti, Tupitsyna, Av, Khrunin, Sa, Limborska
Publikováno v:
Europe PubMed Central
The aim of our investigation was to study the connection between p53 gene Bam HI RFLP polymorphism and the brain infarction volume in patients with atherothrombotic ischemic stroke that could highlight certain genetic aspects of the individual sensib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0d38965084df2635815cc355ce3c64cb
https://pubmed.ncbi.nlm.nih.gov/15272143
https://pubmed.ncbi.nlm.nih.gov/15272143
Autor:
Vi, Skvortsova, Sa, Limborskaia, Petr Slominsky, Lv, Gubskiĭ, Ea, Kol Tsova, Im, Shetova, Na, Shamalov, Ti, Tupitsina, Ia, Platonova
Publikováno v:
Europe PubMed Central
A significant association between Bam HI RFLP p53 gene polymorphism and brain infarction volume in patients with atherothrombotic ischemic stroke (AIS) from Moscow population was found. Biallelic Bam HI polymorphism in exon 5 of p53 gene was studied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4bf66a68f4f1a0a9016afdcc6c5b81ee
https://pubmed.ncbi.nlm.nih.gov/12830514
https://pubmed.ncbi.nlm.nih.gov/12830514