نتایج جستجو برای: ag and gg genotypes were 005

تعداد نتایج: 16860919  

Journal: :World journal of emergency medicine 2015
Liang-Shan Peng Juan Li Gao-Sheng Zhou Lie-Hua Deng Hua-Guo Yao

BACKGROUND Triggering receptor expressed on myeloid cells-1 (TREM-1) is a cell surface receptor expressed on neutrophils and monocytes. TREM-1 acts to amplify inflammation and serves as a critical mediator of inflammatory response in the context of sepsis. To date, the predisposition of TREM-1 gene polymorphisms to septic shock has not been reported. This study was designed to investigate wheth...

2012
Torsak Bunupuradah Mayumi Imahashi Thatri Iampornsin Kazuhiro Matsuoka Yasumasa Iwatani Thanyawee Puthanakit Jintanat Ananworanich Jiratchaya Sophonphan Apicha Mahanontharit Tomoki Naoe Saphonn Vonthanak Praphan Phanuphak Wataru Sugiura

INTRODUCTION Human APOBEC3G is a host defense factor that potently inhibits HIV replication. We hypothesize that HIV-infected children with a genetic variant of APOBEC3G will have a more rapid disease progression. METHODS Antiretroviral therapy (ART)-naïve children, aged 1-12 years old with CD4 15-24% and without severe HIV-related symptoms were enrolled. The children had CD4% and absolute CD...

Journal: :Egyptian Journal of Medical Human Genetics 2022

Abstract Background Gestational diabetes mellitus is the most common metabolic dysfunction that arises during pregnancy. GDM can lead to serious health complications for both mother pregnancy and after delivery of baby. Additionally, mother–offspring suffers from abnormalities in metabolism. The study aimed investigate glutathione S?transferase P1 ghrelin genetic variants pregnant women diagnos...

2013
Robin Haring Henri Wallaschofski Alexander Teumer Heyo Kroemer Angela E Taylor Cedric H L Shackleton Matthias Nauck Uwe Völker Georg Homuth Wiebke Arlt

DHEA is the major precursor of human sex steroid synthesis and is inactivated via sulfonation to DHEAS. A previous genome-wide association study related the single nucleotide polymorphism (SNP) rs2637125, located near the coding region of DHEA sulfotransferase, SULT2A1, to serum DHEAS concentrations. However, the functional relevance of this SNP with regard to DHEA sulfonation is unknown. Using...

2013
Farzian Aminuddin Tillie-Louise Hackett Dorota Stefanowicz Aabida Saferali Peter D Paré Amund Gulsvik Per Bakke Michael H Cho Augusto Litonjua David A Lomas Wayne H Anderson Terri H Beaty Edwin K Silverman Andrew J Sandford

BACKGROUND Due to the pleiotropic effects of nitric oxide (NO) within the lungs, it is likely that NO is a significant factor in the pathogenesis of chronic obstructive pulmonary disease (COPD). The aim of this study was to test for association between single nucleotide polymorphisms (SNPs) in three NO synthase (NOS) genes and lung function, as well as to examine gene expression and protein lev...

2017
Gaurav Parihar Deepak Sharma Satyendra Pal Singh Madhu Tiwari Rakesh Goel Sanjeev Kumar Singh Vijay Pandey

The objective of the present study was to investigate the polymorphism in 5′ non-coding region of growth hormone receptor (GHR) gene in Sahiwal (n = 53) and Hariana (n = 50) cattle using NsiI/PCR-RFLP assay. Amplification of DNA sample revealed 302bp product using specific primer pairs and digested by using NsiI restriction enzyme. All the screened animals were found monomorphic in nature for G...

Journal: :American journal of epidemiology 2006
Sandra K Pope Stephen B Kritchevsky Christine Ambrosone Kristine Yaffe Frances Tylavsky Eleanor M Simonsick Caterina Rosano Scott Stewart Tamara Harris

Myeloperoxidase, an antimicrobial enzyme, produces oxidative free radicals. Rarely found in normal brain tissue, myeloperoxidase has been detected in microglia associated with Alzheimer's disease plaques. The authors examined a G-463A polymorphism in the promoter region of the myeloperoxidase gene (MPO) to determine the relation of MPO variants to cognitive decline over 4 years in a cohort of a...

جعفرزاده, عبدالله, جمالی, میترا, رستمی‌راد, مهدی, صفا, امین, مهدوی, رؤیا, ناصری, محسن,

Background: Multiple sclerosis (MS) is a chronic inflammatory disorder of the CNS characterized by destruction of the myelin sheath, gliosis and progressive neurological dysfunction. The regulatory T (Treg) cells play a major role in the control of the autoimmunity and inflammation. The forkhead box p3 (FOXP3) is a central molecule in the function of Treg cells that play an important role in th...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2014
Xiao-Lian Zhang Yu Lu Shi Yang Qi-Liu Peng Jian Wang Li Xie Yan Deng Yu He Tai-Jie Li Xue Qin Shan Li

BACKGROUND Various studies have evaluated the relationship between X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln polymorphism and hepatocellular carcinoma (HCC) risk, but the conclusions have been inconsistent and underpowered. The purpose of this updated meta-analysis was to examine whether XRCC1 Arg399Gln polymorphism confers susceptibility to HCC. METHODS Eligible studies extr...

2017
Guo-Chang Liu Zhen-Jian Zhuo Shi-Bo Zhu Jinhong Zhu Wei Jia Zhang Zhao Jin-Hua Hu Jing He Feng-Hua Wang Wen Fu

Wilms' tumor is the most common childhood renal malignancy. A genome-wide association study identified LIM domain only 1 (LMO1) as having oncogenic potential. We examined the associations between LMO1 gene polymorphisms and susceptibility to Wilms' tumor. In this hospital-based, case-control study, we recruited 145 children with Wilms' tumor and 531 cancer-free children. Four polymorphisms (rs1...

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