نتایج جستجو برای: rs1799983

تعداد نتایج: 76  

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...

Background: The transversion of G to T (G894T) in human endothelial nitric oxide synthase (eNOS) gene has profound effects such as male infertility, recurrent miscarriage, multiple sclerosis and cardiovascular diseases.Objectives: Development of a new Multiplex Tetra-Primer Amplifi cation Refractory Mutation System - Polymerase Chain Reaction (T-ARMS-PCR) for detection of...

2014
Rafael Amorim Belo Nunes Lúcia Pereira Barroso Alexandre da Costa Pereira José Eduardo Krieger Alfredo José Mansur

BACKGROUND Treadmill exercise test responses have been associated with cardiovascular prognosis in individuals without overt heart disease. Neurohumoral and nitric oxide responses may influence cardiovascular performance during exercise testing. Therefore, we evaluated associations between functional genetic polymorphisms of α-adrenergic receptors, endothelial nitric oxide synthase, bradykinin ...

2016
Tandi E Matsha Carmen Pheiffer Tinashe Mutize Rajiv T Erasmus Andre P Kengne

The aim of this study is to quantify global DNA methylation and investigate the relationship with diabetes status and polymorphisms in MTHFR C677T and NOS3 G894T genes in mixed ancestry subjects from South Africa. Global DNA methylation was measured, and MTHFR rs1801133 and NOS3 rs1799983 polymorphisms were genotyped using high throughput real-time polymerase chain reaction and direct DNA seque...

Journal: :Genetics and molecular research : GMR 2015
J Y Li F Tao X X Wu Y Z Tan L He H Lu

Impaired antioxidant defense increases the oxidative stress and contributes to the development of type 2 diabetes mellitus (T2DM). MnSOD and eNOS are important antioxidant enzymes. This aim of this study was to verify the association of MnSOD and eNOS tagSNPs with T2DM in a Chinese Han population. Four tagSNPs of MnSOD and eight tagSNPs of eNOS were detected using TaqMan technology in 1272 heal...

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: :Genetics and molecular research : GMR 2013
L Luo D H Li S G Wei H B Zhang S B Li J Zhao

Endothelial nitric oxide synthase (eNOS) is an enzyme that influences placental human chorionic gonadotropin production during gestation. Previous studies have indicated an association between eNOS activity, implantation, and maintenance of pregnancy, but proposed associations between polymorphisms of the eNOS gene and recurrent miscarriage (RM) are controversial. To identify markers contributi...

2014
Wei Shen Jiang Du Bin Wang Qiyi Zeng

AIM To evaluate the association of NOS1 and NOS3 gene polymorphisms with the risk/severity of neonatal respiratory distress syndrome (RDS) among preterm infants. METHODS The patient group was 189 preterm infants diagnosed with RDS. The control group was 227 preterm neonates who did not develop RDS. NOS genotyping was performed using an improved multiplex ligation detection reaction (iMLDR) te...

2011
Radenka Kuzmanić Šamija Dragan Primorac Biserka Rešić Bernarda Lozić Vjekoslav Krželj Maja Tomasović Eugenio Stoini Ljubo Šamanović Benjamin Benzon Marina Pehlić Vesna Boraska Tatijana Zemunik

AIM To test the association of NOS3 gene with hypoxic-ischemic encephalopathy (HIE). METHODS The study included 110 unrelated term or preterm born children (69 boys and 41 girls) with HIE and 128 term and preterm born children (60 boys and 68 girls) without any neurological problems after the second year of life. Children with perinatal HIE fulfilled the diagnostic criteria for perinatal asph...

2017
Jie Zhao Wen Zhang Li Shen Xiaomeng Yang Yi Liu Zhongtao Gai

Mycoplasma pneumoniae is a common cause of community-acquired pneumonia (CAP) and the clinical presentation of mycoplasma pneumoniae pneumonia (MPP) varies widely. Genetic variability affecting the host response may also influence the susceptibility to MPP. Several studies have investigated the association between single nucleotide polymorphism (SNP) of some genes and the risks of CAP; however,...

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