نتایج جستجو برای: ag and gg genotypes were 005

تعداد نتایج: 16860919  

2017
Shanqun Jiang Scott A. Venners Kang Li Yi-Hsiang Hsu Justin Weinstock Yanfeng Zou Faming Pan Xiping Xu

We investigated the associations of LEP G2548A and LEPR Q223R polymorphisms with statin-induced creatine kinase (CK) elevation among Chinese patients with hyperlipidemia. A total of587 enrolled individuals were treated with 20 mg/d oral simvastatin for 8 consecutive weeks. Genotyping of LEP G2548A and LEPR Q223R were conducted using PCR-RFLP. Multiple regression analyses showed that, in the Don...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2014
Xiaoyan Li Xiangnan Kong Liyu Jiang Tingting Ma Shi Yan Cunzhong Yuan Qifeng Yang

BACKGROUND Calcium-sensing receptor (CaSR) is a typical G protein coupled receptor. The rs17251221 SNP is located in an intron of the CaSR gene, and the G allele is considered a gain of function mutation. Previous studies revealed that rs17251221 polymorphisms contribute to the risk of developing certain types of cancers. This study investigated the rs17251221 SNP in breast cancer by analyzing ...

2015
Shuxia Guo Yunhua Hu Yusong Ding Jiaming Liu Mei Zhang Rulin Ma Heng Guo Kui Wang Jia He Yizhong Yan Dongsheng Rui Feng Sun Lati Mu Qiang Niu Jingyu Zhang Shugang Li Paul Tchounwou

We have investigated the relationship between the polymorphisms and haplotypes in the CETP gene, and dyslipidemia among the Xinjiang Kazak and Uyghur populations in China. A total of 712 patients with dyslipidemia and 764 control subjects of CETP gene polymorphism at rs12149545, rs3764261, rs1800775, rs711752, rs708272, rs289714, rs5882, and rs1801706 loci were studied by the Snapshot method, l...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهرکرد - دانشکده علوم پایه 1392

سندرم متابولیک از اختلالات رایج در کودکان است که با مجموعه ای از فاکتورهای خطر چون چاقی، افزایش قند خون، تری گلیسرید، فشار خون و کاهش کلسترول hdl همراه است. ژن mir-33b به همراه ژن میزبان خود، srebf-1، به عنوان یک تنظیم کننده اصلی در حفظ حالت پایدار کلسترول سلول و تنظیم مسیر سیگنالینگ انسولین شناخته شده است؛ بنابراین به عنوان یک ژن کاندید برای ابتلا به سندرم متابولیک می تواند مورد بررسی قرار گیر...

2016
Chao Qin Qiang Cao Pu Li Shangqian Wang Jian Wang Meilin Wang Haiyan Chu Liqun Zhou Xuesong Li Dingwei Ye Hailiang Zhang Yiran Huang Baijun Dong Xiaofeng Sun Qing Zou Hongzhou Cai Lijiang Sun Jian Zhu Fade Liu Junbiao Ji Li Cui Xiaoxiang Wang Hai Zhou Hu Zhao Bin Wu Jianchun Chen Minjun Jiang Zhengdong Zhang Pengfei Shao Xiaobing Ju Changjun Yin

The purpose of the present study was to investigate whether genetic variants that influence angiogenesis and sorafenib pharmacokinetics are associated with clinical outcomes and toxic effects in advanced renal cell carcinoma patients treated with this drug. One hundred patients with advanced renal cell carcinoma were enrolled. Forty-two polymorphisms in 15 genes were selected for genotyping and...

Journal: :DNA and cell biology 2008
Rodrigo Mattos dos Santos Carlos Márcio Nóbrega de Jesus José Carlos Souza Trindade Filho José Carlos Souza Trindade João Lauro Viana de Camargo Cláudia Aparecida Rainho Silvia Regina Rogatto

The aim of the present study was to examine the impact of polymorphisms in prostate-specific antigen (PSA) and androgen-related genes (AR, CYP17, and CYP19) on prostate cancer (PCa) risk in selected high-risk patients who underwent prostate biopsy. Blood samples and prostate tissues were obtained for DNA analysis. Single-nucleotide polymorphisms in the 50-untranslated regions (UTRs) of the PSA ...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009
Kenneth A Perkins Caryn Lerman Melissa Mercincavage Carolyn A Fonte Jessica L Briski

Genes coding for nicotinic acetylcholine receptors may influence response to nicotine replacement therapy for smoking cessation. We examined the association of a 3' untranslated region polymorphism (rs2072661) in the nicotinic acetylcholine receptor beta2 subunit (CHRNB2) gene with quitting success in response to nicotine versus placebo patch during a short-term test of patch effects. In a with...

Background: The decisive etiology of Oral squamous cell carcinoma (OSCC)  is still ambiguous, but we recognize the contribution of genetic aberration and environmental agent due to OSCC initiation. In the current study, we elucidate the potential impact of EGFR gene polymorphisms in the risk of OSCC in the southeast of Iran. Methods: Forty-eight OSCC patients along with 100 normal volunteers w...

Journal: :The journal of international advanced otology 2017
Kübra Şeker Yıldız Kasım Durmuş Gonca Dönmez Serdal Arslan Emine Elif Altuntaş

OBJECTIVE The aim of the present study was to investigate whether there was any relationship between some DNA N-methyltransferase 1 (DNMT1) polymorphisms and susceptibility to idiopathic sudden sensorineural hearing loss (ISSHL) in ISSHL patients. MATERIAL AND METHODS We investigated 90 patients diagnosed with ISSHL and a control group composed of 75 age- and gender-matched healthy individual...

Journal: :international journal of reproductive biomedicine 0
zeinab nematollahi hossein hadinedoushan abbas aflatoonian gilda eslami nasrin ghasemi

background: recurrent pregnancy loss (rpl) has been defined as two or more miscarriages before 20 th week of gestation. it seems that il-27 may reduce inflammatory responses and affect the survival of the embryo during human pregnancy. il-27 polymorphisms may influence rpl by altering the levels or the activity of gene product. objective: we studied for the first time the association of il-27 -...

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