Zobrazeno 1 - 10
of 41
pro vyhledávání: '"V N, Maximov"'
Autor:
A. A. Ivanova, S. K. Malyutina, V. P. Novoselov, I. A. Rodina, O. V. Khamovich, V. N. Maximov
Publikováno v:
Атеросклероз, Vol 17, Iss 1, Pp 7-11 (2021)
The aim of the research is to verify the association with sudden cardiac death (SCD) of single nucleotide polymorphisms rs10867772 and rs4700290, identified as new molecular genetic markers of SCD in the own genome-wide pooled allelotyping. Materi
Externí odkaz:
https://doaj.org/article/baad71ff22a6409cbd366f3ba80a404b
Autor:
A. A. Kuznetsov, E. E. Tsvetkova, A. A. Kuznetsova, V. N. Maximov, D. V. Denisova, M. I. Voevoda
Publikováno v:
Атеросклероз, Vol 16, Iss 1, Pp 9-13 (2020)
Pulse wave amplification and augmentation are considered as new indicators of arterial stiffness. It is of interest to study their association with electrocardiographic pro-arrhythmic patterns in the male population of Novosibirsk. Material and me
Externí odkaz:
https://doaj.org/article/2c7766c04cc04705a83f62473c6eb67c
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 7 (2021)
Atrial fibrillation (AF) is one of the most common tachyarrhythmias, contributing to both environmental and genetic factors, a clear understanding of which can be extremely important for determining management tactics and predicting the disease cours
Externí odkaz:
https://doaj.org/article/c359f941454244e995506d9dd87f393a
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 11, Iss 2, Pp 37-41 (2019)
Objective: to study the association of DRD2/ANKK1 Taq1A polymorphism with depression in an open 45–64-year-old male population from Novosibirsk.Patients and methods. A representative sample of an open 45–64-year-old male population (n=781) was su
Externí odkaz:
https://doaj.org/article/2b5affe3b0924032b5e03d851fb6d0ab
Autor:
P. S. Orlov, D. Е. Ivanoshchuk, А. А. Ivanova, S. К. Malyutina, V. P. Novosyolov, М. I. Voevoda, V. N. Maximov
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 59-63 (2018)
Aim. Assessment of the associations of mononucleotide polymorphisms (MNP) of genes: KCNN2 (rs13184658, rs10076582, rs338625) and NOS1AP (rs12567209, rs348624, rs3751284, rs 12143842), with sudden cardiac death (SCD), and evaluation of the clutch unit
Externí odkaz:
https://doaj.org/article/3fc7cffa27a94490a8758fb3578b6549
Publikováno v:
Патология кровообращения и кардиохирургия, Vol 23, Iss 1, Pp 83-85 (2019)
Письмо редакторуФибрилляция предсердий (ФП), наряду с хронической сердечной недостаточностью и сахарным диабетом, отнесена мировым мед
Externí odkaz:
https://doaj.org/article/0207301f66cb43de9459f37d26c886a3
Publikováno v:
Медицинская иммунология, Vol 19, Iss 2, Pp 185-190 (2017)
Search for molecular genetic markers of risk and prognosis of breast cancer is an important prospective of modern research. Many molecular mechanisms are involved in pathogenesis of breast cancer and define a wide range of possible candidate genes. T
Externí odkaz:
https://doaj.org/article/98012831a853408aa1aacb0b0a16eb9d
Publikováno v:
Ateroscleroz. 17:35-42
Aim of the study was to investigate the associations of polymorphisms of some genes with overweight and some anthropometric and biochemical indicators in a population sample of the young population of Novosibirsk. Material and methods. The study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::435cd1d5a54ba26d9d8f9445ddb9d9a8
https://doi.org/10.52727/2078-256x-2021-17-4-35-42
https://doi.org/10.52727/2078-256x-2021-17-4-35-42
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 18, Iss 4/2, Pp 847-855 (2015)
The research concerns the task of identification of contrasted single nucleotide polymorphisms (SNPs) obtained in genome-wide pooled allelotyping of 16 human cohorts, comprising healthy and ill persons, by the nested case–control approach. The geno
Externí odkaz:
https://doaj.org/article/66dcb12dd4c9420d90b6ee7c6687d13f
Autor:
V N, Maximov, P S, Orlov, A A, Gurazeva, E S, Melnikova, V V, Gafarov, O A, Chervova, M I, Voevoda, S K, Malyutina
Publikováno v:
Advances in gerontology = Uspekhi gerontologii. 35(3)
We studied the relationship between the leucocyte telomere length (LTL) and the copy number of mitochondrial DNA (CNmtDNA) and the development of acute coronary syndrome during 15 years of follow-up. A random population sample was examined at baselin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bafccd3e6de2dfd66f46b4a5f35b8866
https://pubmed.ncbi.nlm.nih.gov/36169361
https://pubmed.ncbi.nlm.nih.gov/36169361