Zobrazeno 1 - 10
of 34
pro vyhledávání: '"A. A. Semenchukov"'
Autor:
A. V. Popov, A. A. Semenchukova
Publikováno v:
Vestnik MGSU, Vol 18, Iss 11, Pp 1683-1691 (2023)
Introduction. Within the framework of this study, an important and interesting period of the development of higher school architecture in our country is considered, characterized by an integrated approach and the mass introduction of advanced solutio
Externí odkaz:
https://doaj.org/article/163e976f3cd9443d859cf7a5e0de45fe
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, 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
Autor:
S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, D. A. Nikulin, A. A. Semenchukov, O. V. Marilovceva, S. S. Tret'jakova, I. I. Lebedeva, V. N. Maksimov
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 14, Iss 4, Pp 488-493 (2018)
Background. The search for genetic predictors of stroke development is actively studied in all developed countries due to the need to address the primary prevention of socially significant diseases. Gene CYP17A1 is one of the many genes that can part
Externí odkaz:
https://doaj.org/article/9c96c56c37ca44b18acb8776e914775a
Autor:
S. Yu. Nikulina, A. A. Chernova, D. A. Nikulin, V. A. Shulman, S. V. Prokopenko, I. M. Platunova, O. V. Marilovceva, I. I. Lebedeva, A. A. Semenchukov, D. A. Yakovleva, V. N. Maksimov, A. V. Kuskaeva
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 14, Iss 4, Pp 509-514 (2018)
Background. The study of the incidence of risk factors (RF) of stroke for primary and secondary prevention of this disease remains relevant. There are modifiable and non-modifiable RF.Aim. To study the frequency of the main RF in patients with ischem
Externí odkaz:
https://doaj.org/article/ac295d4022a147b9abf3caa2cf39b3a6
Autor:
E. V. Lychkovskaya, A. N. Shuvaev, G. E. Gercog, L. V. Trufanova, L. B. Shadrina, A. A. Semenchukov, A. B. Salmina
Publikováno v:
Бюллетень сибирской медицины, Vol 17, Iss 1, Pp 191-198 (2018)
In the process of evolution of eukaryotes has formatted a highly organized mechanism for maintaining and regulating intracellular calcium homeostasis, which is one of the most important components of cell signaling in all branches of the phylogenetic
Externí odkaz:
https://doaj.org/article/b6b6a71ff7984275a295c4211f5f9232
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 13, Iss 5, Pp 597-601 (2017)
Background. The discovery of new genetic predictors of cardiovascular diseases can be used in predicting and diagnosing latent forms of the disease. Wolff-Parkinson-White syndrome (WPW) occurs in all age groups and detected in 1-30 people per 10000,
Externí odkaz:
https://doaj.org/article/b194791878d84af4921e93768b5e0ede
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
Autor:
D. A. Nikulin, O. V. Marilovceva, V. A. Shulman, I. I. Lebedeva, Vladimir N. Maksimov, S. S. Tret'jakova, A. A. Chernova, S. Yu. Nikulina, A. A. Semenchukov
Publikováno v:
Racionalʹnaâ Farmakoterapiâ v Kardiologii, Vol 14, Iss 4, Pp 488-493 (2018)
Background. The search for genetic predictors of stroke development is actively studied in all developed countries due to the need to address the primary prevention of socially significant diseases. Gene CYP17A1 is one of the many genes that can part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a35d06887801e2c7c1e8b2c08738fad4
https://doi.org/10.20996/1819-6446-2018-14-4-488-493
https://doi.org/10.20996/1819-6446-2018-14-4-488-493
Autor:
A. A. Semenchukov, D. A. Nikulin, I. I. Lebedeva, S. V. Prokopenko, A. V. Kuskaeva, I. M. Platunova, D. A. Yakovleva, Vladimir N. Maksimov, A. A. Chernova, S. Yu. Nikulina, V. A. Shulman, O. V. Marilovceva
Publikováno v:
Racionalʹnaâ Farmakoterapiâ v Kardiologii, Vol 14, Iss 4, Pp 509-514 (2018)
Background. The study of the incidence of risk factors (RF) of stroke for primary and secondary prevention of this disease remains relevant. There are modifiable and non-modifiable RF.Aim. To study the frequency of the main RF in patients with ischem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24b962729898a22405362234ce701f51
https://www.rpcardio.com/jour/article/view/1719
https://www.rpcardio.com/jour/article/view/1719