نتایج جستجو برای: ga and aa genotype

تعداد نتایج: 16841203  

2016
Dilshad Ahmad

Cigarette smokingis the root cause of cancer and death from lung cancer. Singlenucleotidepolymorphisms(SNPs) are the salient location in an individual genome which influences the diseases. Since cigarette smoke contain large number of oxidants which may induce mutations. Bcl-2 SNPs have been found to be associated with predisposition of different cancers. In present study we examine the associa...

Journal: :avicenna journal of medical biotechnology 0

background: acromegaly is associated with increased morbidity and mortality related to cardiovascular diseases. leptin (lep) and leptin receptor (lepr) gene polymorphisms can increase cardiovascular risks. the aim of this study was to investigate association between the frequencies of lep and lepr gene polymorphisms and subclinical atherosclerosis in acromegalic patients. methods: forty-four ac...

2016
Qianqian Liu Shouquan Wu Miao Xue Andrew J. Sandford Jingcan Wu Yu Wang Guo Chen Chuanmin Tao Yin Tang Yulin Feng Jun Luo Jian-Qing He

Phagocyte Nicotinamide Adenine Dinucleotide Phosphate (NADPH) oxidase complex is a key enzyme that catalyzes the production of reactive oxygen species, which mediate oxygen-dependent killing of microorganisms, such as Mycobacterium tuberculosis. P22phox, encoded by CYBA, is the key regulatory subunit of NADPH oxidase. Our study aimed to investigate the association of CYBA polymorphisms with sus...

Journal: :International journal of clinical and experimental pathology 2015
Bateer Han Zhanlin Guo Ying Ma Shirong Kang Yufei Wang Qiyou Wei Xu Wu

We investigated the association between the clinical outcome and GSTP1 and XRCC1 gene polymorphisms in advanced NSCLC patients with cisplatin-based chemotherapy. We prospectively recruited 325 NSCLC patients between January 2010 and January 2014. Genotypes of GSTP1 A313G, XRCC1 Arg194Trp, Arg280His and Arg399Gln were conducted using polymerase chain reaction restriction fragment length polymorp...

ژورنال: دانشور پزشکی 2018
اکبر زاده باغبان, رضا, خاکسار, لیلا, طباطبایی پناه, پردیس سادات,

Background and Objective: Alopecia Areata (AA) is characterized by an autoimmune hair loss usually, but not limited to, the scalp, affecting approximately 1-2% of the general population. Although the etiology and pathogenesis of this disease is still unknown, it is known that TNFα-308G/A polymorphism can influence the development of AA. The aim of this study was to investigate TNF-α(rs1800629) ...

Journal: :Genetics and molecular research : GMR 2015
G-C Shi L-G Zhang

We conducted a case-control study in a Chinese population to examine the correlations between interleukin (IL)-17 gene polymorphisms and tuberculosis (TB) development. The study population included 336 TB subjects and 351 control subjects who were enrolled between June 2012 and June 2014. Genotyping analyses of IL-17A rs2275913 and rs3748067 and IL-17F rs763780 were analyzed using polymerase ch...

2016
Chi-Ming Tai Chih-Kun Huang Hung-Pin Tu Jau-Chung Hwang Ming-Lun Yeh Chung-Feng Huang Jee-Fu Huang Chia-Yen Dai Wan-Long Chuang Ming-Lung Yu

The patatin-like phospholipase domain-containing protein 3 (PNPLA3) variant is associated with nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). However, the role of genetic variations of the peroxisome proliferator-activated receptor gamma coactivator-1-alpha gene (PPARGC1A) and glucokinase regulatory (GCKR) gene on NASH in obese patients remains unclear. We stu...

2012
Sarah L. Prior Amy R. Clark Danielle A. Jones Steve C. Bain Steve J. Hurel Steve E. Humphries Jeffrey W. Stephens

PPAR-γ co-activator-1α (PGC-1α) is a tissue-specific transcriptional co-activator involved in the regulation of antioxidant enzymes. The A-allele of the rs8192678 PGC-1 α} (G>A) gene variant has previously been associated with nephropathy in Korean and Indian-Asian type 2 diabetes mellitus (T2DM) samples. Our aim was to examine the association between this variant and urine albumin exccretion i...

Schizophrenia is a mental disorder characterized by abnormal social behavior and failure to understand reality. The aim of this study was to determine the relation between FOLH1 and DISC1 genes polymorphism in patients with schizophrenia in Iran. In this study, 50 patients with schizophrenia and 50 healthy controls were evaluated. PCR-RFLP was used for FOLH1 gene and Tetra-ARMS for the DIS...

Mojgan Mohammadi, Philip J.R. Day

Background: The pathogenesis of many diseases is correlated to irregularity in vascular endothelial growth factor (VEGF) expression. Results from several association studies show that variation in the level of VEGF expression is related to polymorphic sequences within the VEGF gene. Additionally, there are many studies showing that some gene polymorphisms significantly influence the pharmacokin...

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