Zobrazeno 1 - 10
of 29
pro vyhledávání: '"S S. Tretyakova"'
Autor:
S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S S. Tretyakova, A. A. Semenchukov, O. V. Marilovtseva, I. I. Lebedeva, V. N. Maksimov, A. A. Gurazheva
Publikováno v:
Терапевтический архив, Vol 92, Iss 12, Pp 25-30 (2020)
Aim.To study the association of single-nucleotide polymorphismrs3025058(5а/6а) with the development of stroke in patients of the East Siberian population with cardiovascular pathology and risk factors for its development. Materials and methods.T
Externí odkaz:
https://doaj.org/article/14f9e73ff8be4db8a2890b3e76e982bb
Autor:
S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S. S. Tretyakova, V. N. Chernov, O. V. Marilovtseva, A. N. Kelemeneva, V. N. Maksimov, A. A. Gurazheva
Publikováno v:
Бюллетень сибирской медицины, Vol 19, Iss 1, Pp 85-93 (2020)
The aim of the study was to investigatey the association of single-nucleotide polymorphism (SNP) rs10507391 (A>T) with the acute cerebrovascular accident (CVA) development in patients of the East Siberian population with cardiovascular pathology and
Externí odkaz:
https://doaj.org/article/516078d0f85b41f7a63f529ca6a8d656
Autor:
S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S. S. Tretyakova, V. N. Maksimov, A. A. Gurazheva
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 15, Iss 5, Pp 634-640 (2019)
Aim. To study the association of single nucleotide polymorphism rs556621 (G> T) with development of stroke in patients of the East Siberian population with cardiovascular pathology and risk factors.Material and methods. The study involved 260 patient
Externí odkaz:
https://doaj.org/article/8c83998032c24eacb11def8a3113d8ff
Autor:
S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S. S. Tretyakova, A. A. Semenchukov, O. V. Marilovtseva, V. N. Maksimov, A. А. Gurazheva
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 29-34 (2019)
Aim. To study the association of single nucleotide polymorphism (SNP) rs2230806 (C>T) with the development of acute cerebrovascular accident (CVA) in East Siberian patients with cardiovascular pathology and risk factors.Material and methods. The stud
Externí odkaz:
https://doaj.org/article/fc2ac91451414f8eac1307ba837f9648
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 53-58 (2018)
Aim. To study the possibility of using the genotypes of the TBX5 gene as independent variables for predicting the development of idiopathic disorders of atrioventricular and intraventricular conduction in individuals of the East Siberian population.M
Externí odkaz:
https://doaj.org/article/59113390fda24f07975a8c5e38996f2a
Autor:
S. Yu. Nikulina, O. V. Marilovtseva, A. A. Chernova, S. S. Tretyakova, D. A. Nikulin, V. N. Maksimov
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 32-36 (2016)
Aim. To study the association of polymorphisms rs1800795 of gene IL-6 with the development of sick sinus node syndrome (SSS).Material and methods. Totally, 109 patients studied, with idiopathic SSS, and 59 of their healthy relatives of I, II, III gra
Externí odkaz:
https://doaj.org/article/9e6b9e965d034180854862b924ddca2d
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 30-34 (2015)
Aim. To study relation of mononucleotide polymorphism G>A of the gene SCN10A and development of inherited pathology of the heart conduction system.Material and methods. Totally, 260 persons investigated with primary disorders of cardiac conduction (7
Externí odkaz:
https://doaj.org/article/3535ad74ab4747fc899fcb597eeb87c2
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 46-49 (2015)
Aim. To study the relation of mononucleotide polymorphism G?C (rs619203) of ROS1 gene with the risk of ischemic and hemorrhagic stroke development.Material and methods. Totally 152 patients studied (92 males, 60 females) with acute brain circulation
Externí odkaz:
https://doaj.org/article/9bd29200bacc41118561b27e68a09e91
Autor:
S. S. Tretyakova, S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, V. N. Maksimov, M. I. Voevoda, V. N. Chernov
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 82-86 (2014)
Aim. To study relationship of idiopathic atrioventricular and intravenricular disorders of cardiac conductivity with mononucleotide polymorhism (MNP) A/G gene TBX5. Material and methods. Totally 260 persons with primary cardiac conductivity disorders
Externí odkaz:
https://doaj.org/article/8556605f3b8a4c90a3c054b8c0413ac0
Autor:
S. Yu. Nikulina, A. N. Kelemeneva, D. A. Nikulin, A. A. Chernova, I. M. Platunova, V. A. Shulman, A. A. Semenchukov, S. S. Tretyakova, S. V. Prokopenko, O. V. Marilovtseva, Vladimir N. Maksimov, A. A. Gurazheva
Publikováno v:
"Arterial’naya Gipertenziya" ("Arterial Hypertension"). 25:549-556
The stroke is one of the most serious complications of arterial hypertension (HTN). Genetic markers of the disease can be used to improve the risk stratification. According to the literature data of single nucleotide polymorphism (SNP) rs12204590 (T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e4fe7e2f16dfb7d8313ab60674b3fbc
https://doi.org/10.18705/1607-419x-2019-25-5-549-556
https://doi.org/10.18705/1607-419x-2019-25-5-549-556