Zobrazeno 1 - 10
of 87
pro vyhledávání: '"AGT gene"'
Autor:
PABLO C.S. FARIAS, LEANDRO P. CABRAL, PATRÍCIA A.F. NEVES, CAIO A.B. JANUÁRIO, BEATRIZ M. CORDEIRO, WILSON J. DA SILVA JÚNIOR, CAROLINA BASEGGIO, SÉRGIO S.L. PAIVA JÚNIOR, PAULO S.R. DE ARAÚJO, VIRGÍNIA MARIA B. DE LORENA, VALDIR Q. BALBINO, REGINALDO G. LIMA NETO
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 96, Iss suppl 3 (2024)
Abstract The COVID-19 pandemic has been the largest pandemic of the past century, and various genetic factors have played a significant role in this context. This study aimed to analyze the frequency and association between specific SNPs rs3806268 (N
Externí odkaz:
https://doaj.org/article/bb6a936e0b5c4803a29b3057653e21b9
Autor:
Muhammad Sajid Hamid Akash, Momina Shahid, Shaleem Suhail, Kanwal Rehman, Ahmed Nadeem, Tahir Maqbool Mir
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Background and purposeHypertension (HTN) is a multifactorial chronic disease that poses a significant global health burden and is associated with increased mortality rates. It often coexists with other conditions, such as cardiovascular, liver, and r
Externí odkaz:
https://doaj.org/article/ddc9b748188f4943aed11804dcfb6ab9
Autor:
Sargylana Sofronova, Maria Kirillina, Irina Kononova, Anna Romanova, Vyacheslav Nikolaev, Sardana Kononova
Publikováno v:
International Journal of Biomedicine, Vol 9, Iss 4, Pp 287-291 (2019)
The research objective was to study the association of the AGT rs699 missense SNP with arterial hypertension (AH) and metabolic risk factors among indigenous people of the Arctic territory of Yakutia. The obtained data show that representatives of in
Externí odkaz:
https://doaj.org/article/8c4843ba9470462684d0af0041538c8f
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 27, Iss 4, Pp 401-411 (2019)
The aim of our study was to evaluate the association between variant genotype of angiotensinogen (AGT) c.-58A>C, lifestyle factors and clinical factors and corporeal extension of gastric inflammatory and preneoplastic lesions.
Externí odkaz:
https://doaj.org/article/9de88a79a0184d1f8ec5fe01bfe45cfe
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
Autor:
Shin-Yu Lin, Gwo-Tsann Chuang, Chien-Hui Hung, Wei-Chou Lin, Yung-Ming Jeng, Ting-An Yen, Karine Chang, Yin-Hsiu Chien, Wuh-Liang Hwu, Chien-Nan Lee, I-Jung Tsai, Ni-Chung Lee
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Oligohydramnios is not a rare prenatal finding. However, recurrent oligohydramnios is uncommon, and genetic etiology should be taken into consideration. We present two families with recurrent fetal oligohydramnios that did not respond to amnioinfusio
Externí odkaz:
https://doaj.org/article/42a8b80ea674456d843c3634343abc16
Akademický článek
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Akademický článek
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Publikováno v:
Thai Journal of Obstetrics and Gynaecology, Vol 25, Iss 1, Pp 52-61 (2017)
Objectives:This study aims to determine the relationship between angiotensinogen (AGT) M235T polymorphism and hypertension among post-menopausal Thai women.Materials and Methods: Case-control study was conducted. The study group was those who had hyp
Externí odkaz:
https://doaj.org/article/6ce8ebfa992344d295acd445555f7223
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