Zobrazeno 1 - 10
of 46
pro vyhledávání: '"rs2200733"'
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
A previous genome-wide association study (GWAS) has reported that variants rs2200733 and rs6843082 in the paired-like homeodomain transcription factor 2 (PITX2) gene may be one of the risk factors for ischemic stroke (IS) in European populations. How
Externí odkaz:
https://doaj.org/article/cfb3745c41bb4ec9b4db712208a3e9d0
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 4, Pp 30-37 (2020)
Aim: to study the association of rs2200733 polymorphism with antiarrhythmic efficacy of amiodarone, propafenone and allapinin in the prevention of atrial fibrillation (AF) progression.Material and methods. In order to comparatively evaluate the effec
Externí odkaz:
https://doaj.org/article/708b329f76b44912b7f347eb1e3a01a4
Publikováno v:
Терапевтический архив, Vol 93, Iss 1, Pp 41-43 (2021)
Aim. To study the significance of the rs1378942 polymorphisms of the CSK gene and rs2200733 (chromosome 4q25) in the progression of AF in men with AH and AO. Materials and methods. In an observational cohort study, 116 men aged 4565 years were fol
Externí odkaz:
https://doaj.org/article/88a9da61d0a64acf96dc0fc4e482ea2a
Publikováno v:
Паёми Сино, Vol 21, Iss 2, Pp 238-246 (2019)
Objective: To study genetic determinants in patients with atrial fibrillation (AF) on the background of arterial hypertension (AH) in combination with various extracardiac comorbid pathology. Methods: In a prospective cohort study included 167 pat
Externí odkaz:
https://doaj.org/article/94e339885f504338ae739b1adb0e94e4
Autor:
Natalya Valeryevna Aksyutina, Vladimir Abramovich Shulman, Elena Evgenevna Aldanova, Elena Yurievna Pelipeckaya, Sergey Sergeevich Petrov, Vasily Vladimirovich Kozlov, Nikolay Andreevich Stepanov
Publikováno v:
Siberian Journal of Life Sciences and Agriculture, Vol 11, Iss 2, Pp 124-138 (2019)
After studying the Association of the TT genotype and the T allele with the development of lone atrial fibrillation (AF) and constructing a logistic regression model, it was revealed that the probability share of lone AF in the presence of the TT gen
Externí odkaz:
https://doaj.org/article/09f0b62a8fce4ba784a54d23b0fe8abf
Autor:
Vladimir A. Shulman, Natalya V. Aksyutina, Elena A. Aldanova, Svetlana Yu. Nikulina, Vasily V. Kozlov, Larissa G. Soinova, Oksana A. Gavrilyuk
Publikováno v:
International Journal of Biomedicine, Vol 8, Iss 4, Pp 280-283 (2018)
The aim of our case-control study was to investigate the possible genetic association of the rs2200733 SNP on chromosome 4q25 with AF in the Russian population as this association has not been examined before in this ethnicity. Methods and Results:
Externí odkaz:
https://doaj.org/article/68cdc12be09044ca8904eb197234347f
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:
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
Akademický článek
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Publikováno v:
Терапевтический архив, Vol 93, Iss 1, Pp 41-43 (2021)
To study the significance of the rs1378942 polymorphisms of the CSK gene and rs2200733 (chromosome 4q25) in the progression of AF in men with AH and AO.In an observational cohort study, 116 men aged 4565 years were followed. Of these, 57 patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03fac33a93c737027984fc8b7e0751b7
https://pubmed.ncbi.nlm.nih.gov/33720624
https://pubmed.ncbi.nlm.nih.gov/33720624