Zobrazeno 1 - 10
of 134
pro vyhledávání: '"agtr2"'
Autor:
Li Wang, Robert M. Rossi, Xiaoting Chen, Jing Chen, Jilian Runyon, Mehak Chawla, Daniel Miller, Carmy Forney, Arthur Lynch, Xuzhe Zhang, Fansheng Kong, Bo Jacobsson, Leah C. Kottyan, Matthew T. Weirauch, Ge Zhang, Louis J. Muglia
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-12 (2023)
Abstract Background Preterm birth (PTB), defined as delivery before 37 gestational weeks, imposes significant public health burdens. A recent maternal genome-wide association study of spontaneous PTB identified a noncoding locus near the angiotensin
Externí odkaz:
https://doaj.org/article/be5cdb1ceca847a8807404f5cbf105e9
Publikováno v:
운동과학, Vol 31, Iss 1, Pp 105-109 (2022)
Purpose This study aimed to investigate the association between AGTR2 (rs11091046 A>C) gene polymorphism and athletic performance. Methods The Korean national team cyclists enrolled in the study performed 30-second Wingate test (peak power, mean powe
Externí odkaz:
https://doaj.org/article/0e2294a22de647edb5c44d349649fff6
Autor:
Nongthombam Boby, Xuewei Cao, Kelsey Williams, Shiva Kumar Goud Gadila, Monica N. Shroyer, Peter J. Didier, Sudesh K. Srivastav, Arpita Das, Kate Baker, Qiuying Sha, Bapi Pahar
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Angiotensin converting enzyme-2 (ACE2) and associated proteins play a pivotal role in various physiological and pathological events, such as immune activation, inflammation, gut barrier maintenance, intestinal stem cell proliferation, and apoptosis.
Externí odkaz:
https://doaj.org/article/c46204a529e04467be250943fd6fb087
Autor:
A. L. Khokhlov, A. N. Yavorsky, N. O. Pozdnyakov, J. V. Rybachkova, E. S. Emelianov, A. A. Khokhlov, A. E. Miroshnikov, S. O. Pozdnyakov
Publikováno v:
Архивъ внутренней медицины, Vol 8, Iss 1, Pp 45-52 (2018)
The complexity of therapy of lipid metabolism disorders is not only in comorbidity and polypragmasia, but also in predicting a genetically determined response to the treatment. The aim of our work was to study the pharmacogenetics features of pharmac
Externí odkaz:
https://doaj.org/article/31bf942db4b14a65a049a70b29d53deb
Autor:
Alfred R. Bogdanov, Svetlana A. Derbeneva, Olga O. Cherniak, Alexandra A. Bogdanova, Kamilat M. Gapparova, Olga N. Grigorian
Publikováno v:
Ожирение и метаболизм, Vol 16, Iss 1, Pp 39-46 (2019)
BACKGROUND: the study of molecular genetic markers and pathogenetic mechanisms of neurohormonal activation, as well as their importance in the formation of heart failure in obesity, is an urgent problem of modern medicine, the solution of which will
Externí odkaz:
https://doaj.org/article/c0cdef05a4a34a478a9bb1b8ef7deb55
Akademický článek
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Autor:
Jevnikar, Kristina
Znanstvena izhodišča Marca 2020 je bila razglašena pandemija koronavirusne bolezni 19 (COVID-19), ki jo povzroča virus SARS-CoV-2. Bolezen primarno prizadane respiratorni sistem, najpogosteje v obliki hude obojestranske pljučnice, v sklopu okuž
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3505::5fccb96be0ded167092a08996331ae0c
https://repozitorij.uni-lj.si/Dokument.php?id=169986&dn=
https://repozitorij.uni-lj.si/Dokument.php?id=169986&dn=
Autor:
Lütfiye Özpak, Ayfer Pazarbaşı, Nurşen Keser, M. Bertan Yılmaz, H. Ümit Lüleyap, Fatime Tuncay Özgünen
Publikováno v:
Cukurova Medical Journal, Vol 42, Iss 3, Pp 477-483 (2017)
Amaç: Preeklampsi, tüm gebeliklerin yaklaşık %6-10’ unda görülen ve gebe kadınlara özgü ciddi bir hastalıktır. İmmün ve genetik faktörlerin de katkıda bulunduğu kompleks bir hastalıktır. Bu çalışmada amacımız, AGTR2A1675G ve
Externí odkaz:
https://doaj.org/article/6f9f8940fd2f4c91b7c9e873435d3602
Publikováno v:
Архивъ внутренней медицины, Vol 6, Iss 3, Pp 53-58 (2016)
Coronary heart disease (CHD) is a major cause of mortality. Morphological substrate of CHD in most cases is atherosclerosis, which is based on structural genes polymorphism eNOS and AGTR2. The aim of the study was to study the prevalence of eNOS and
Externí odkaz:
https://doaj.org/article/08921629dd5143edac7fbcd13fcc5630
The article presents the results of a comparison of clinical and molecular genetic data on the study of the role of polymorphism of the genes of the renin-angiotensin system - ADD1, AGT, AGTR1, AGTR2, CYP11B2, GNB3, NOS3 in children with essential ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a76f056790ca65c201314ade9bff587