نتایج جستجو برای: ga and aa genotype

تعداد نتایج: 16841203  

Journal: :avicenna journal of neuro psycho physiology 0
azar ejmalian school of medicine, hamadan university of medical sciences, hamadan, ir iran massoud saidijam department of molecular medicine and genetics, school of medicine, hamadan university of medical sciences, hamadan, ir iran amir keshavarzi research center for behavioral disorders and substances abuse, hamadan university of medical sciences, hamadan, ir iran mohammad ahmadpanah research center for behavioral disorders and substances abuse, hamadan university of medical sciences, hamadan, ir iran leila jahangard research center for behavioral disorders and substances abuse, hamadan university of medical sciences, hamadan, ir iran nooshin shabab department of molecular medicine and genetics, school of medicine, hamadan university of medical sciences, hamadan, ir iran

background bipolar disorder is a biological brain disorder which is associated with debilitating fluctuation in mood and adverse effects on patients, their families and society. the importance of genetics and its role in bipolar disorder is a controversial issue to discuss. evidence indicates a relation between the risk of bipolar disorder and specific genes. amongst the genes whose role has be...

برخورداری, عسگر, حسن‌زاده, تقی,

Background: Coronary heart disease (CHD) is a leading cause of death worldwide and hypertriglyceridemia and hypercholesterolemia are major risk factors for the disease. Considering the role of hyperlipidemia as the underlying cause of cardiovascular mortalities and morbidities, and the limited and conflicting results of studies on CETP gene polymorphisms in Iran, we aimed to study -971 G/A poly...

Journal: :iranian journal of basic medical sciences 0
liou cao department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china shan mou department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china wei fang department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china chaojun qi department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china xinbei chang department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china leyi gu department of nephrology, molecular cell laboratory for kidney disease, renji hospital, school of medicine, shanghai jiao tong university, shanghai center for peritoneal dialysis research, shanghai, china

objective(s):the aim of the study was to investigate the relationship between insulin resistance (ir) and leptin (lep) gene polymorphisms in peritoneal dialysis (pd) patients. materials and methods: from july 1, 2011 to august 1, 2011, patients who received chronic pd were chosen and divided into three groups (dm, high homr-ir, and low homr-ir). two pcr products of lep were sequenced and aligne...

Journal: :Cardiovascular Diabetology 2009
Barry R Palmer Courtney L Devereaux Sukhbir S Dhamrait Tessa J Mocatta Anna P Pilbrow Chris M Frampton Lorraine Skelton Tim G Yandle Christine C Winterbourn A Mark Richards Hugh E Montgomery Vicky A Cameron

BACKGROUND A variant in the promoter of the human uncoupling protein 2 (UCP2) gene, the G-866A polymorphism, has been associated with future risk of coronary heart disease events, in those devoid of traditional risk factors and in those suffering from diabetes. We thus examined the impact of the G-866A polymorphism on 5-year survival in a cohort of 901 post-myocardial infarction patients, and t...

2016
Ying Li Qian Xu Jingwei Liu Caiyun He Quan Yuan Chengzhong Xing Yuan Yuan

The relationship between the pri-let-7a-1 rs10739971 polymorphism and gastric cancer (GC) risk has been reported. However, the role of this polymorphism in the prognosis of GC remains largely elusive. Sequenom MassARRAY platform method and the polymerase chain reaction (PCR)-restriction fragment length polymorphism were used to investigate pri-let-7a-1 rs10739971 G→A in 334 GC patients. Real-ti...

Journal: :international journal of reproductive biomedicine 0
robab davar nasim tabibnejad seyed mehdi kalantar mohammad hasan sheikhha

background: despite extensive progress in ivf techniques, one of the most difficult problems is the variability in the response to controlled ovarian hyperstimulation (coh). recent studies show the effects of individual genetic variability on coh outcome. objective: to evaluate the correlation between lhβ g1502a polymorphisms in exon 3 of the lh gene and ovarian response to coh. materials and m...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2007
Hiroshi Hirata Yuji Hinoda Nobuyuki Kikuno Ken Kawamoto Angela V Dahiya Yutaka Suehiro Yuichiro Tanaka Rajvir Dahiya

PURPOSE The chemokine CXCL12 and its receptor CXCR4 have been found to be associated with cancer metastasis. A single nucleotide polymorphism of CXCL12 G801A has been described and is regarded as a target for cis-acting factor that has the ability to up-regulate CXCL12 expression. Currently, there are no reports investigating the role of CXCL12 G801A polymorphism in prostate cancer (PC). EXPE...

Journal: :International journal of clinical and experimental pathology 2015
Lanjie Yao Shuli Xing Xueqin Fu Hongjie Song Zhendong Wang Jianrong Tang Yongjing Zhao

We conducted a case-control study to investigate the association between three common SNPs in IL-10 gene (rs1800896, rs1800871 and rs1800872) and the development of liver cirrhosis in a Chinese population. Between January 2013 and December 2014, a total of 318 patients with liver cirrhosis and 318 health control subjects were enrolled into our study. The IL-10 rs1800896, rs1800871 and rs1800872...

2016
Cristina Oana Mărginean Claudiu Mărginean Septimiu Voidăzan Lorena Meliţ Andrei Crauciuc Carmen Duicu Claudia Bănescu

The aim of this study was to establish the manner in which the LEPR 223, 1019, 492, and 976 gene polymorphisms influence child obesity.We performed a prospective case-control study on 264 hospitalized children from Romania (Nutrichild study) whom we divided into 2 groups: Group I -143 controls and Group II-121 obese children.The 2 groups were evaluated regarding the anthropometry (MUAC, TST, H/...

Journal: :International journal of clinical and experimental pathology 2015
Lian Shuang Zhiliang Li Fengying Chen Xiaoying Cui Yuzhen Ning Youle Su Mei Dong

We conducted a case-control study to estimate the association between IL-17A rs2275913, rs3819025 and rs3748067 polymorphisms and development of coronary artery disease. A total of 415 patients with coronary artery disease and 448 health controls were recruited during the period of March 2013 and October 2014. Genotyping of IL-17A rs2275913, rs3819025 and rs3748067 were analyzed by polymerase c...

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