نتایج جستجو برای: rs2070744

تعداد نتایج: 47  

2011
T Okochi T Kishi M Ikeda T Kitajima Y Kinoshita K Kawashima T Okumura T Tsunoka Y Fukuo T Inada M Yamada N Uchimura M Iyo I Sora N Ozaki H Ujike N Iwata

Endothelial nitric oxide synthase (NOS3) is one of the enzymes influencing nitric oxide (NO) function in the human brain. NO is a gaseous neurotransmitter that is involved in a variety of mechanisms in the central nervous system, such as N-methyl-D-aspartate receptor activation and oxidative stress. The evidence from animal pharmacological studies and postmortem studies supports an association ...

2015
Charlotta Ryk Lotta Renström Koskela Tomas Thiel N. Peter Wiklund Gunnar Steineck Martin C. Schumacher Petra J. de Verdier

PURPOSE Bacillus Calmette-Guérin (BCG)-treatment is an established treatment for bladder cancer, but its mechanisms of action are not fully understood. High-risk non-muscle invasive bladder-cancer (NMIBC)-patients failing to respond to BCG-treatment have worse prognosis than those undergoing immediate radical cystectomy and identification of patients at risk for BCG-failure is of high priority....

2011
Jae Hee Kang Janey L. Wiggs Jonathan Haines Wael Abdrabou Louis R. Pasquale

PURPOSE To investigate whether associations with the nitric oxide synthase gene (NOS3) variants and risk of primary open-angle glaucoma (POAG) depend on female reproductive factors. METHODS Two functional and two tagging single nucleotide polymorphisms (SNPs; T-786C: rs2070744, Glu298Asp: rs1799983, rs7830, and rs3918188) were evaluated in a nested case-control study from the Nurses' Health S...

Journal: :Clinical science 2009
Ying Xin Xiaodong Song Hao Xue Zhe Liu Xiaojian Wang Hu Wang Kai Sun Yongyi Bai Junhao Liu Rutai Hui

eNOS (endothelial NO synthase) plays a critical role in the development of ventricular remodelling and cardiac hypertrophy. The purpose of the present study was to determine whether three common variants in NOS3 (the eNOS gene) are associated with the risk of LVH [LV (left ventricular) hypertrophy] in patients with essential hypertension. Three NOS3 genetic variants, -T786C (rs2070744), eNOS4a/...

2010
Amy Z Fan Jing Fang Ajay Yesupriya Man-huei Chang Greta Kilmer Meaghan House Donald Hayes Renée M Ned Nicole F Dowling Ali H Mokdad

PURPOSE Epidemiologic studies suggest that several gene variants increase the risk of stroke, and population-based studies help provide further evidence. We identified polymorphisms associated with the prevalence of self-reported stroke in US populations using a representative sample. METHODS Our sample comprised US adults in the Third National Health and Nutrition Examination (NHANES III) DN...

2012
Johanna Weiss Stephan A. Fränkl Josef Flammer Matthias C. Grieshaber Gabor Hollo Barbara Teuchner Walter Emil Haefeli

PURPOSE Substantial evidence suggests that ocular perfusion is regulated by nitric oxide (NO), and polymorphisms in genes encoding for enzymes involved in NO formation and degradation (endothelial nitric oxide synthase [NOS3] and cytochrome b-235 alpha polypeptide gene [CYBA]) might contribute to vascular dysregulation observed in glaucoma. We therefore assessed the association of glaucoma with...

Journal: :Genetics and molecular research : GMR 2014
K Zhou Y Wang W Peng J Sun Y M Qing X M Mo

The endothelial NO synthase (eNOS) enzyme is expressed during the early stages of cardiogenesis and plays an important role in normal heart development. Genetic variations of eNOS G894T have been shown to influence individual susceptibility to some phenotypes of congenital heart disease (CHD) in different populations. We conducted a case-control study comprised of 945 CHD patients and 972 non-C...

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...

2017
N. G. Kukava B. V. Titov G. J. Osmak N. A. Matveeva O. G. Kulakova A. V. Favorov R. M. Shakhnovich M. Ya. Ruda O. O. Favorova

In search of genetic markers of myocardial infarction (MI) risk, which have prognostic significance for Russians, we performed a replication study of MI association with genetic variants of PCSK9 (rs562556), APOE (epsilon polymorphism, rs7412 and rs429358), LPL (rs320), MTHFR (rs1801133), eNOS (rs2070744), and the 9p21 region (rs1333049) in 405 patients with MI and 198 controls. Significant MI ...

2014
Bruno Schmidt Dellamea Cristiane Bauermann Leitão Rogério Friedman Luis Henrique Canani

About 30% of patients with type 2 diabetes mellitus develop clinically overt nephropathy. Hyperglycemia is necessary, but not sufficient, to cause the renal damage that leads to kidney failure. Diabetic nephropathy (DN) is a multifactorial disorder that results from interaction between environmental and genetic factors. In the present article we will review the role of the nitric oxide synthase...

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