نتایج جستجو برای: rs2070744

تعداد نتایج: 47  

Journal: :Journal of psychopharmacology 2015
Sarah Kittel-Schneider Martin Reuß Andrea Meyer Heike Weber Alexandra Gessner Carolin Leistner Juliane Kopf Brigitte Schmidt Susanne Hempel Julia Volkert Klaus-Peter Lesch Andreas Reif

INTRODUCTION Several studies have shown altered levels of nitric oxide (NO) and its stable metabolites (NOx (-)) in blood and cerebrospinal fluid of psychiatric patients. The aim of our study was to replicate previous findings and investigate the influence of the nitrinergic system in bipolar disorder and adult attention-deficit/hyperactivity disorder (aADHD) in particular. METHODS The concen...

2016
Yang Xiang Yi Dong Xuan Li Xin Tang

Purpose. To clarify the association of endothelial nitric oxide synthase (eNOS) polymorphisms and primary open angle glaucoma (POAG). Methods. After a systematic literature search in the MEDLINE, EMBASE, and ISI Web of Science databases, all relevant studies evaluating the association between the polymorphisms (rs2070744 and rs1799983) of eNOS gene and POAG were screened and included. The poole...

2016
Yongqin Wu Zhiling Zhu Xiaoxia Fang Ling Yin Yuxia Liu Shouxia Xu Aixue Li

Endothelial NOS (NOS3) has a potential role in the prevention of neuronal injury in hypoxic-ischemic encephalopathy (HIE). Thus, we aimed to explore the association between NOS3 gene polymorphisms and HIE susceptibility and symptoms in a Chinese Han population. Three single nucleotide polymorphisms (SNPs) in the NOS3 gene, rs1800783, rs1800779, and rs2070744, were detected in 226 children with ...

Journal: :Genetics and molecular research : GMR 2016
G L Zhao Q J Li H Y Lu

The enzyme endothelial nitric oxide synthase (NOS3) is an important mediator of atherosclerotic disease and is associated with coronary artery disease (CAD). There is growing evidence that polymorphisms in NOS3 influence the progression of CAD; however, there is also a controversy regarding the association of polymorphisms in the gene encoding NOS3 and CAD. To determine if the NOS3 genetic vari...

2014
S Güler H Gürkan H Tozkir N Turan Y Çelik

We investigated the phenotype-genotype association of the following endothelial nitric oxide synthase (eNOS) gene polymorphisms, rs743506, rs2070744, rs1799983, rs180079, rs3918226, rs207468799 and rs148554851, in patients suffering from migraine living in Edirne, Turkey. A total of 175 individuals, who had been diagnosed with migraine between April 2013 and December 2013, at the Neurology Depa...

2017
Mohammad Mehdi Heidari Mehri Khatami Yaser Tahamtan

Introduction Multiple Sclerosis (MS) is a disease of central nervous system that mainly causes lesions or plaques in the spinal cord and brain. The purpose of this study was to analyze the relation between c.-813C>T (rs2070744) and c.894G>T (rs1799983) polymorphisms of NOS3 gene and MS in Iranian patients. Methods A total of 78 patients with MS and 80 healthy controls were screened for NOS3 (...

Journal: :Journal of Education, Health and Sport 2021

Objective: to evaluate the association of essential arterial hypertension (EAH) and its severity with genes polymorphism NOS3 (rs2070744) GNB3 (rs5443) in West-Ukrainian population.
 Materials methods. One-hundred EAH patients (48 – healthy control) participated cohort case-control study. Blood pressure (BP), Creatinine, glucose, lipids panel were studied. genotyping performed by TaqMan pr...

Journal: :Hypertension 2012
Marcelo R Luizon Ingrid F Metzger Riccardo Lacchini Jose E Tanus-Santos

Endothelial Nitric Oxide Synthase Polymorphism rs3918226 Associated With Hypertension Does Not Affect Plasma Nitrite Levels in Healthy Subjects To the Editor: Salvi et al reported that the single nucleotide polymorphism (SNP) rs3918226 in the promoter of the endothelial NO synthase (eNOS) gene was associated with hypertension. Although no functional studies show how this SNP affects eNOS, the a...

Journal: : 2022

More than 50% of patients with essential arterial hypertension (EAH) have additionalcardiovascular risk factors, among which the most common are obesity, diabetes mellitus,metabolic syndrome, etc.Objective – to investigate polymorphic variants NOS3 (rs2070744) and GNB3(rs5443) genes as markers obesity in EAH patients.Material methods. 100 48 practically healthy (control group)participated study...

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