نتایج جستجو برای: genotype frequencies

تعداد نتایج: 180285  

2016
Xiao-juan Nie Wen-min Liu Li Zhang

BACKGROUND Cutaneous squamous cell carcinoma (cSCC) is the second most common type of non-melanoma skin cancer (NMSC) globally. The aims of this study were to further systematically clarify the potential association of rs833061 (-460 C>T) and rs1570360 (-1154 G>A), two SNPs of VEGF, with the risk of cSCC and the prognostic impacts on cSCC patients. MATERIAL AND METHODS This hospital-based case-...

زمانی, علیرضا, سعیدی جم, مسعود, علیخانی, محمدیوسف, غفاری, محمد ابراهیم, فرهادی کهن, حامد, محمودی, حسن, کاظمی, سیما, کرامت, فریبا,

Background and purpose: Brucellosis is a systemic infection caused by gram-negative coccobacilli and facultative intracellular bacteria of the genus Brucella. Interleukin-17 is one of the important cytokines that plays a role in controlling host immune response in patients with brucellosis. The aim of this study was to investigate polymorphism of the genes encoding IL-17 in patients with brucel...

Journal: :cell journal 0

objective: neuregulin1 (nrg1) gene is among the most promising candidate genes for schizophrenia. this gene is located on 8p22-p12, a region with a reported linkage to schizophrenia. several studies have reported an association between schizophrenia and the 5′ end polymorphisms in this gene. however, some studies have failed to confirm the role of nrg1 gene in the pathogenesis of schizophrenia....

2016
Sahar Tulbah Huda Alabdulkarim Mohammad Alanazi Narasimha Reddy Parine Jilani Shaik Akbar Ali Khan Pathan Abdullah Al-Amri Wajahatullah Khan Arjumand Warsy

The present study aimed at investigating the relationship between rs1801320 (G>C), rs1801321 (G>T), and rs2619681 (C>T) RAD51 gene polymorphisms and the risk of breast cancer development in Saudi females. The genotypes were analyzed using TaqMan genotyping assay and polymerase chain reaction-restriction fragment length polymorphism. The genotype and allele frequencies were computed using chi-sq...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2008
Kelly Cristina de Oliveira Bianca Bianco Ieda T N Verreschi Alexis Dourado Guedes Bianca Borsato Galera Marcial Francis Galera Caio P Barbosa Monica Vannucci Nunes Lipay

BACKGROUND Dysfunctions in the folate metabolism can result in DNA hypomethylation and abnormal chromosome segregation. Two common polymorphisms of this enzyme (C677T and A1298C) reduce its activity, but when associated with aneuploidy studies the results are conflicting. The objective of the present study is to analyze the MTHFR gene polymorphisms in women with Turner Syndrome and in a control...

Journal: :Genetics and molecular research : GMR 2015
V J Picos-Cárdenas E Sáinz-González A Miliar-García A Romero-Zazueta R Quintero-Osuna E Leal-Ugarte V Peralta-Leal J P Meza-Espinoza

The calpain-10 gene is expressed primarily in tissues important in glucose metabolism; thus, some of its polymorphisms have been associated with type 2 diabetes. In this study, we examined the association between the calpain-10 single-nucleotide polymorphism (SNP)-43, SNP-19, and SNP-63 and type 2 diabetes in Mexican mestizos. We included 211 patients and 152 non-diabetic subjects. Polymerase c...

2004
ALAN M BURGESS

Since the introduction of the short acting muscle relaxant succinyl dicholine (suxamethonium) in 1951 and the subsequent discovery that certain patients exhibited a greater than usual sensitivity to the drug, interest has been directed towards identifying the genetically controlled variants of serum cholinesterase (acylcholine acyl hydrolase E.C. 3.1.1.8). Some of these variants have been found...

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