نتایج جستجو برای: snp polymorphism

تعداد نتایج: 116808  

2012
Minkyu Jung Byoung Chul Cho Chul Ho Lee Hyung Soon Park Young Ae Kang Se Kyu Kim Joon Chang Dae Jun Kim Sun Young Rha Joo Hang Kim Ji Hyun Lee

PURPOSE Mutations in the epidermal growth factor receptor (EGFR) have been confirmed as predictors of the efficacy of treatment with EGFR-tyrosine kinase inhibitors (TKIs). We investigated whether polymorphisms of the EGFR gene were associated with clinical outcomes in non-small cell lung cancer (NSCLC) patients treated with EGFR-TKI. MATERIALS AND METHODS A polymorphic dinucleotide repeat in...

Journal: :Genetics and molecular research : GMR 2013
M Y Yu P Q Zhao X H Yan B Liu Q Q Zhang R Wang C H Ma X H Liang F L Zhu L F Gao

Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is expressed in different tissues and cells, including the pancreas and lymphocytes, and it can selectively induce apoptosis in tumor cells but not in most normal cells. TRAIL plays critical roles in type 1 diabetes mellitus, and is involved in type 2 diabetes mellitus (T2DM). We recently discovered the association of nonalco...

Journal: :iranian journal of biotechnology 2008
mohammad ronaghi sadeq vallian masoud etemadifar

a single nucleotide polymorphism (snp) in cd24 has been associated with multiple sclerosis (ms) in a population based study. this snp results in the replacement of alanine (cd24a) by valine (cd24v) at amino acid 57 in the resulting polypeptide chain. in the current study, the genotyping of this snp and its contribution to ms in 217 patients and 200 healthy individuals of an iranian population w...

Ali Mohammad Foroughmand, Hamid Galehdari, Khadijeh Golabgir Khademi, Mahdi Pourmahdi Borujeni, Parvaneh Dinarvand, Saied Yazdankhah, Zahra Shahbazi,

Background: Coronary artery disease (CAD) is a multifactorial and heterogenic disease. Recently, genome-wide association studies have reported that rs1333040 (C/T) and rs1004638 (A/T) single nucleotide polymorphisms (SNPs) in the 9p21 locus have very strong association with CAD. This study aimed to examine these associations in Southwest of Iran. Methods: Blood samples were collected from 200 C...

2017
Pantaporn Supakankul Tanavadee Kumchoo Supamit Mekchay

OBJECTIVE This study was conducted to identify and evaluate the effective single nucleotide polymorphism (SNP) markers for fat deposition in the longissimus dorsi muscles of pigs using the amplified fragment length polymorphism (AFLP) approach. METHODS Sixty-four selective primer combinations were used to identify the AFLP markers in the 20 highest- and 20 lowest-intramuscular fat (IMF) conte...

2011
Tamuno Alfred Yoav Ben-Shlomo Rachel Cooper Rebecca Hardy Cyrus Cooper Ian J Deary Jane Elliott David Gunnell Sarah E Harris Mika Kivimaki Meena Kumari Richard M Martin Chris Power Avan Aihie Sayer John M Starr Diana Kuh Ian N M Day

Several age-related traits are associated with shorter telomeres, the structures that cap the end of linear chromosomes. A common polymorphism near the telomere maintenance gene TERT has been associated with several cancers, but relationships with other aging traits such as physical capability have not been reported. As part of the Healthy Ageing across the Life Course (HALCyon) collaborative r...

Journal: :Archives of internal medicine 2006
Bernd Jilma Florian M Kovar Gregor Hron Georg Endler Claudia L Marsik Sabine Eichinger Paul A Kyrle

BACKGROUND The single nucleotide polymorphism (SNP) Ser128Arg in the E-selectin gene is overrepresented in certain patient populations with atherosclerosis or restenosis. As this SNP enhances tissue factor-triggered coagulation in humans during systemic inflammation, we hypothesized that it may also predispose for the development of recurrent venous thromboembolism (VTE). METHODS A total of 5...

2017
Matej Horvat Uros Potocnik Katja Repnik Rajko Kavalar Vesna Zadnik Stojan Potrc Borut Stabuc

BACKGROUND Colorectal cancer (CRC) represents one of the most common malignancies worldwide. Research has indicated that functional gene changes such as single nucleotide polymorphism (SNP) influence carcinogenesis and metastasis and might have an influence on disease relapse. The aim of our study was to evaluate the role of SNPs in selected genes as prognostic markers in resectable CRC. PATI...

2013
Silvano Presciuttini Alessandro Gialluisi Serena Barbuti Michele Curcio Fabrizio Scatena Giancarlo Carli Enrica L. Santarcangelo

Higher brain dopamine content depending on lower activity of Catechol-O-Methyltransferase (COMT) in subjects with high hypnotizability scores (highs) has been considered responsible for their attentional characteristics. However, the results of the previous genetic studies on association between hypnotizability and the COMT single nucleotide polymorphism (SNP) rs4680 (Val(158)Met) were inconsis...

Journal: :Neuroscience & Biobehavioral Reviews 2014
F. Harrisberger K. Spalek R. Smieskova A. Schmidt D. Coynel A. Milnik M. Fastenrath V. Freytag L. Gschwind A. Walter T. Vogel K. Bendfeldt D.J.-F. de Quervain A. Papassotiropoulos S. Borgwardt

BACKGROUND The brain-derived neurotrophic factor (BDNF) Val66Met polymorphism (refSNP Cluster Report: rs6265) is a common and functionally relevant single nucleotide polymorphism (SNP). The gene itself, as well as the SNP rs6265, have been implicated in hippocampal learning and memory. However, imaging genetic studies have produced controversial results about the impact of this SNP on hippocamp...

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