Zobrazeno 1 - 10
of 190
pro vyhledávání: '"Mi, Voevoda"'
Autor:
Vn, Maximov, Sofia Malyutina, Ps, Orlov, Ivanoschuk DE, Sv, Mikhailova, My, Shapkina, Hubacek J, Holmes M, Bobak M, Mi, Voevoda
Publikováno v:
Europe PubMed Central
We used quantitative real-time PCR method to analyse mtDNA copy number in a random subsample (n=996; 358 men aged 66,31±7,24 years; 468 women aged 67,62±7,1 years) selected from a population cohort (n=9 630) examined at baseline in international pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e5f43a185aa0b1f38847ff4427649e0a
https://pubmed.ncbi.nlm.nih.gov/31512430
https://pubmed.ncbi.nlm.nih.gov/31512430
Publikováno v:
Europe PubMed Central
The purpose of the research was studying of leukocyte telomere length association with age, sex, risk factors for age-related diseases in Russian people of pre-retirement and retirement age. By quantitative real-time PCR method we studied the leukocy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::810c32426276c428d1e6de02609aa7d9
https://pubmed.ncbi.nlm.nih.gov/28556637
https://pubmed.ncbi.nlm.nih.gov/28556637
Publikováno v:
Europe PubMed Central
The polymorphism of mtDNA was examined in populations of Old Believers (n = 104) and Russians from Novosibirsk oblast (n = 270). Most of the haplogroups identified belonged to West Eurasian lineages. The frequencies of these haplogroups constituted 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9e52f282017bca994f074b9eb8451229
https://pubmed.ncbi.nlm.nih.gov/25715465
https://pubmed.ncbi.nlm.nih.gov/25715465
Publikováno v:
Europe PubMed Central
The article deals with data on association of SNP rs1828591 of HHIP gene with COLD development under exposure to dust and chemical factors. SNP rs1800470 of TGFbeta1 gene is associated with occupational COLD under exposure to dust and did not show co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::775d2a35b7b9f048a46cff49b4824e62
https://pubmed.ncbi.nlm.nih.gov/25073350
https://pubmed.ncbi.nlm.nih.gov/25073350
Autor:
In, Grigor Eva, Tm, Nikitenko, Av, Tikhonov, Ti, Romanova, Vn, Maksimov, Elena Shakhtshneider, Sk, Maliutina, Mi, Voevoda
Publikováno v:
Europe PubMed Central
The paper presents the data available in the literature on mutations in known genes in pancreatitis, such as cationic trypsinogen (PRSS1), pancreatic secretory trypsin inhibitor (PSTI/SPINK1), cystic fibrosis (CFTR), and apolipoprotein E (APOE) genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::343aa14eaa3788073115937833fb2f60
https://pubmed.ncbi.nlm.nih.gov/20387681
https://pubmed.ncbi.nlm.nih.gov/20387681
Autor:
Tn, Kuznetsova, Mi, Voevoda, Oa, Podkolodnaia, Iv, Kulikov, Vf, Kobzev, Sn, Ustinov, Sk, Maliutina, Ni, Logvinenko, Zhuravskaia EIa, Nadezda Cherdyntseva, Tumanov IuV, Oa, Morozova, Va, Baum, Ag, Romashchenko
Publikováno v:
Europe PubMed Central
Analysis of deletion polymorphism of human c-fms gene intron 11 (approximately 425-bp deletion) is of particular interest because of the increased proportion of the deletion heterozygotes among the infants born from the parents, one of which lacks th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::11f8cd28a201e6096256c75695770aa0
https://pubmed.ncbi.nlm.nih.gov/15027206
https://pubmed.ncbi.nlm.nih.gov/15027206
Publikováno v:
Europe PubMed Central
The worsening of the health status of northern populations is a matter of concern to scientists in many countries. International collaboration aimed at using international experience in the field of circumpolar health may speed up the research, makin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::277c35fd43fde8223343cb0a1eca46a3
https://pubmed.ncbi.nlm.nih.gov/10093375
https://pubmed.ncbi.nlm.nih.gov/10093375
Autor:
Ivanoshchuk DE, Ev, Shakhtshneider, Alla Ovsyannikova, Sv, Mikhailova, Od, Rymar, Vi, Oblaukhova, Aa, Yurchenko, Mi, Voevoda
Publikováno v:
Europe PubMed Central
Vavilov Journal of Genetics and Breeding
Vavilov Journal of Genetics and Breeding
The article presents a variant of maturity onset diabetes of the young type 2, caused by a rare mutation in the GCK gene. Maturity onset diabetes of the young (MODY) is a hereditary form of diabetes with an autosomal dominant type of inheritance, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8d5de4c0c100544b511ee80e2e45ef09
http://europepmc.org/abstract/med/33659812
http://europepmc.org/abstract/med/33659812
Autor:
Vm, Perel Muter, Mv, Zav Ialova, Sv, Vtorushin, Em, Slonimskaia, Ng, Kritskaia, Garbukov EIu, Nv, Litviakov, Mn, Stakheeva, Nn, Babyshkina, Ea, Malinovskaia, Ev, Denisov, Es, Grigor Eva, Ms, Nazarenko, Sv, Sennikov, Ep, Goreva, Va, Kozlov, Mi, Voevoda, Vn, Maksimov, Va, Beliavskaia, Nadezda Cherdyntseva
Publikováno v:
Europe PubMed Central
This study involved 525 breast cancer (BC) patients of T2-4N0-2M0 stages at the age of 35 years and older. Significant differences in clinical and pathological characteristics between premenopausal and postmenopausal BC patients were found. Mostly ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8aa3899a783bce75fb3c0dab0c4196ff
http://europepmc.org/abstract/med/19432218
http://europepmc.org/abstract/med/19432218
Publikováno v:
Europe PubMed Central
to study the frequency of alleles and genotypes of APOE gene in women with gallstone disease (GSD), and also to research the association of the APOE gene polymorphism and bile lithogenicity indices.were investigated 104 women after cholecystectomy ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::13e8ab7a54de680ce9c3aafc20559440
http://europepmc.org/abstract/med/20469680
http://europepmc.org/abstract/med/20469680