Zobrazeno 1 - 10
of 15
pro vyhledávání: '"N V Aksyutina"'
Publikováno v:
Терапевтический архив, Vol 89, Iss 9, Pp 48-52 (2017)
Aim. To investigate the AGTR1 A/C polymorphism associated with atrial fibrillation (AF) to form risk groups among patients who are prone to this disease. Subjects and methods. 90 probands with a confirmed diagnosis of AF and their 144 first-, second-
Externí odkaz:
https://doaj.org/article/c0c9c649f2914b479c5df6031f475089
Autor:
V. A. Shulman, S. Yu. Nikulina, N. V. Aksyutina N, E. E. Poplavskaya, B. V. Nazarov, V. N. Maksimov
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 28-31 (2016)
Atrial fibrillation (AF) is one of the most prevalent tachiarrhythmias, with at date non fully understood etiology. Recently, the attention is paid to genetic determinants of AF.Aim. To assess the role of rs2200733 polymorhpism on the chromosome 4q25
Externí odkaz:
https://doaj.org/article/511d63d1706141af91dac0659b919b1d
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 12, Iss 3, Pp 331-336 (2016)
Atrial fibrillation (AF) is the most common heart rhythm disturbance. It is believed that the primary form of AF is genetically determined in most cases, but the genetic component cannot be excluded in the secondary form of AF. AF is a heterogeneous
Externí odkaz:
https://doaj.org/article/97dbcf2b34114fe5b1eccaeab11ed76b
Autor:
N. V. Aksyutina, V. A. Shulman, S. Yu. Nikulina, B. V. Nazarov, V. N. Maksimov, E. V. Plita, M. Yu. Kotlovsky, T. D. Vereshchagina
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 42-45 (2015)
Aim. To assess genetic issues in the ischemic stroke development in AF and to invent an analytical programmed complex for genetic risk estimation of stroke development in a patient with AF.Material and methods. Totally 43 patients studied with AF and
Externí odkaz:
https://doaj.org/article/61213a1a94324ebbadadc21b16276b23
Autor:
V. N. Titov, M. Yu. Kotlovskiy, Ye. V. Kurdoyak, A. V. Yakimenko, I. Yu. Yakimovich, N. V. Aksyutina, Yu. V. Kotlovskiy, A. M. Dygai
Publikováno v:
Бюллетень сибирской медицины, Vol 13, Iss 6, Pp 81-92 (2014)
Irrespective of differences in mechanism of action, hypolipidemic drugs develop their effects according to a single algorithm. They normalize receptor-mediated uptake of polyenic fatty acids (PFA) by cells, thus restoring their functional, regulatory
Externí odkaz:
https://doaj.org/article/1c21c48a6a3349628de289cd134c5a87
Publikováno v:
КардиоСоматика, Vol 7, Iss 2, Pp 21-23 (2016)
The article deals with the issue of genetic determination of atrial fibrillation. In particular, it is shown that a rare polymorphism rs2200733 T allele on chromosome 4q25 statistically more frequently (p=0,029) in patients with atrial fibrillation c
Externí odkaz:
https://doaj.org/article/6007e275fe51464bad0e7929a711333e
Autor:
V. N. Titov, A. M. Dygai, M. Yu. Kotlovskiy, Ye. V. Kurdoyak, A. V. Yakimenko, I. Yu. Yakimovich, N. V. Aksyutina, Yu. V. Kotlovskiy
Publikováno v:
Бюллетень сибирской медицины, Vol 13, Iss 5, Pp 149-159 (2014)
On the basis of phylogenetic theory of general pathology, the cause of a noninfectious disease whose occurrence in a population is more than 5–7% is an impaired biological function or reaction to the environment. From the general biology viewpoint,
Externí odkaz:
https://doaj.org/article/266a77207c0f425b9675a2f265f34c83
Autor:
V. N. Titov, V. A. Amelyushkina, T. A. Rozhkova, M. Y. Kotlovskiy, A. V. Yakimenko, E. V. Kurdoyak, Y. V. Kotlovskiy, N. V. Aksyutina
Publikováno v:
Acta Biomedica Scientifica, Vol 0, Iss 1, Pp 125-130 (2014)
ApoE vector protein in association with apoB-100 directly transferring saturated and monounsaturated FA (SFA and MFA) in triglyceride form (composed of very low density lipoproteins (L)) to the cells which are assimilating FA by cooperative receptors
Externí odkaz:
https://doaj.org/article/091b6abc565645b5a988982d9bc25547
Autor:
N V Aksyutina, Bolshakova T.Yu., E V Kapustina, V S Mordovskii, Pelipetskaya E.Yu., Nikulina S.Yu.
Publikováno v:
"Medical & pharmaceutical journal "Pulse". :60-68
Ankylosing spondylitis is a chronic rheumatological disease of unknown etiology. The search for new genetic associations will improve understanding of pathogenesis. Objective: to study the association of the rs2569190 polymorphism of the CD14 gene wi
Autor:
N. V. Aksyutina, S. Yu. Nikulina, V. A. Shulman, B. V. Nazarov, B. V. Maksimov, A. P. Bezruk, A. I. Balog, E. E. Poplavskaya, A. V. Bespalov, M. Yu. Kotlovskyi, A. A. Chernova
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 6, Pp 6-10 (2013)
Aim. To assess the associations between the polymorphism of the glycoprotein integrin alpha (I
Externí odkaz:
https://doaj.org/article/ba77859559394be6b31c4c3d2de1812a