نتایج جستجو برای: ag and gg genotypes were 005

تعداد نتایج: 16860919  

Ali Movahedi, Alireza Pasdar, Amir Avan, Anne van Krieken, Domenico Rosace, Gordon A. Ferns, Leila Hosseinzadeh, Mahdi Nohtani, Majid Ghayour-Mobarhan, Maryam Pirhoushiaran, Sara Khatamianfar, Seyed Reza Mirhafez, Shiva Ganjali, Valentina Gómez Mellado,

Metabolic syndrome (MetS) is characterized by a cluster of cardiovascular risk factors that include: abdominal obesity, dyslipidaemia, hypertension, insulin resistance and impaired glucose tolerance. Recent genome wide association studies have identified several susceptibility regions involved in lipid metabolism that are also associated with MetS. We have explored the association of 9 genetic ...

Journal: :International journal of clinical and experimental medicine 2015
Xiaoli Lu Xiaowan Chen Jingxu Sun Peng Gao Yongxi Song Xuanzhang Huang Yifan Luo Ping Chen Zhenning Wang

Numerous studies focusing on genetic variants in order to find cetuximab subpopulation biomarkers have emerged, yet the significance of each biomarker is diverse. Based on these results, we carried out a meta-analysis to assess the correlation between epidermal growth factor (EGF) A61G polymorphism and clinical outcomes of metastatic colorectal cancer (mCRC) patients treated with cetuximab. We ...

Journal: :international journal of molecular and cellular medicine 0
seyed reza mirhafez department of basic medical sciences, neyshabur university of medical sciences, neyshabur, iran. amir avan department of modern science and technologies; and biochemistry of nutrition research center; school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) alireza pasdar division of applied medicine, medical school, university of aberdeen, foresterhill, aberdeen, ab25 2zd, uk. sara khatamianfar department of modern science and technologies; and biochemistry of nutrition research center; school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) leila hosseinzadeh department of modern science and technologies; and biochemistry of nutrition research center; school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) shiva ganjali department of modern science and technologies; and biochemistry of nutrition research center; school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

metabolic syndrome (mets) is characterized by a cluster of cardiovascular risk factors that include: abdominal obesity, dyslipidaemia, hypertension, insulin resistance and impaired glucose tolerance. recent genome wide association studies have identified several susceptibility regions involved in lipid metabolism that are also associated with mets. we have explored the association of 9 genetic ...

2015
Parisima Behbahani Seyed Reza Kazemi-Nezhad Ali Mohammad Foroughmand Leila Ahmadi

Linkage studies and epidemiological findings indicate that some possible genes in schizophrenia (SCZ) and bipolar mood disorder (BPD) are common. Numerous evidences for linkage of two diseases on chromosome 22 have been found. These findings suggest that one or more genes in the 22q11.21 region may be involved in the development of both disorders. In the present case-control study, association ...

Journal: :Genetics and molecular research : GMR 2007
M G Thomas R M Enns K L Shirley M D Garcia A J Garrett G A Silver

Sequence polymorphisms in the growth hormone (GH) gene and its transcriptional regulators, Pit-1 and Prop-1, were evaluated for associations with growth and carcass traits in two populations of Brangus bulls Chihuahuan Desert Rangeland Research Center (CDRRC, N = 248 from 14 sires) and a cooperating breeding program (COOP, N = 186 from 34 sires). Polymorphisms were SNP mutations in intron 4 (C/...

Introduction: Sirtuin 1 is a protein deacetylase that plays an important role in many cellular processes. The serum sirtuin 1 levels are higher in the polycystic ovary syndrome (PCOS) patients than the healthy subjects. The aim of this study was to assess the role of SIRT-1 rs7895833 polymorphism in the susceptibility of PCOS. Methods: This case-control study was done on 456 Iranian women fr...

رئیسی, سمیه, شکاری, بنت الهدی,

Background and purpose: Single-nucleotide polymorphisms (SNPs) within miRNA genes may be related with risk of cancer. A main SNP in the pre-miR-27a (rs895819) with an A to G variation was earlier identified. In this study, we aimed to explore any association between SNP rs895819 in the miR-27a gene and breast cancer susceptibility. Materials and methods: This case-control study included 120 br...

2013
Liang-Shan Da Ying Zhang Shuai Zhang Yi-Chun Qian Qin Zhang Feng Jiang Lin Xu

BACKGROUND Single nucleotide polymorphisms (SNPs) may affect the development of diseases. The -2518A/G polymorphism in the regulatory region of the monocyte chemo-attractant protein-1 (MCP-1) gene has been reported to be associated with cancer risk. However, the results of previous studies were inconsistent. Therefore, we performed a meta-analysis to obtain a more precise estimation of the rela...

2018
Agustín Rolandelli Joaquín M Pellegrini Nicolás O Amiano María C Santilli María P Morelli Florencia A Castello Nancy L Tateosian Alberto Levi Nicolás Casco Domingo J Palmero Verónica E García

Interferon gamma (IFNG) plays a key role during Mycobacterium tuberculosis (Mtb) infection, and several polymorphisms located in its gene are associated with risk of tuberculosis in diverse populations. Nevertheless, the genetic resistance/susceptibility to tuberculosis in Argentina is unknown. The IFNG rs1861494 polymorphism (G→A) was reported to alter the binding of transcription factors to t...

Journal: :Cell 2011
Eimear E. Kenny Carlos D. Bustamante

Single-nucleotide variation (SNV) When a single base pair (A, C, T, G) is observed to vary in a DNA sequence. This variant may be private to an individual or family. For biallelic SNVs (i.e., an SNV that exists in two possible states), an individual can carry three possible allelic combinations or genotypes on their two chromosomes (e.g., for a single base pair position that could be A or G, th...

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