نتایج جستجو برای: genotype frequencies

تعداد نتایج: 180285  

2013
Elena García-Martín Oswaldo Lorenzo-Betancor Carmen Martínez Pau Pastor Julián Benito-León Jorge Millán-Pascual Patricia Calleja María Díaz-Sánchez Diana Pisa Laura Turpín-Fenoll Hortensia Alonso-Navarro Lucía Ayuso-Peralta Dolores Torrecillas Elena Lorenzo José Francisco Plaza-Nieto José A G Agúndez Félix Javier Jiménez-Jiménez

BACKGROUND Some recent experimental data suggest a possible role of LINGO-1 in the pathogenesis of multiple sclerosis (MS). In an attempt to identify genetic biomarkers related to MS susceptibility, we genotyped two common SNPs in the LINGO1 gene which have been associated to other neurological conditions, in patients with MS and in healthy subjects. These SNPs are linked to several SNPs within...

2014
Hosik Seok Su Kang Kim Koo Han Yoo Byung-Cheol Lee Young Ock Kim Joo-Ho Chung

Exercise has beneficial effect on cancer apoptosis and benign prostatic hyperplasia (BPH). The BH3 interacting domain death agonist (BID) gene expression is associated with apoptosis or cell proliferation. In this study, we investigated the association between BID single nucleotide polymorphisms (SNPs) and the development, prostate volume, and international prostate symptom score (IPSS) of BPH....

2015
Félix Javier Jiménez-Jiménez Elena García-Martín Hortensia Alonso-Navarro Carmen Martínez Martín Zurdo Laura Turpín-Fenoll Jorge Millán-Pascual Teresa Adeva-Bartolomé Esther Cubo Francisco Navacerrada Ana Rojo-Sebastián Lluisa Rubio Sara Ortega-Cubero Pau Pastor Marisol Calleja José Francisco Plaza-Nieto Belén Pilo-De-La-Fuente Margarita Arroyo-Solera Esteban García-Albea José A.G. Agúndez

Several recent works suggest a possible role of vitamin D deficiency in the etiology or restless legs syndrome (RLS). We analyzed the possible relationship of 2 common single nucleotide polymorphisms (SNPs) in the vitamin D3 receptor (VDR) gene with the risk for RLS.We studied the genotype and allelic variant frequencies of VDR rs2228570 and VDR rs731236 SNPs in 205 RLS patients and 445 healthy...

Journal: :World journal of pediatrics : WJP 2012
Jung Min Ko Seung Yang Se Young Kim Hyo Sung Lee Jin Soon Hwang Il Tae Hwang

BACKGROUND This study was undertaken to evaluate the association of the E23K polymorphism of KCNJ11 and type 1 diabetes in a Korean population. METHODS Clinical variables from 70 Korean children with type 1 diabetes were analyzed. Patients' DNA was screened for the E23 locus in the KCNJ11 gene. Each genotype frequency and clinical characteristics according to the genotypes were compared betwe...

Journal: :Annals of human genetics 1977
F B Livingstone

Although differential contributions to the next generation have frequently been used to measure differences in fitness, a t genetic equilibrium there will be no such differences among genotypes with balanced polymorphism. For a single locus the frequencies, after selection, of the three genotypes, AA, Aa, aa, will be: qlp2/K 2W,,pq/W and W,, q2/v, where v = w,, p2 + 2W,, pq + tyz2 pa. To estima...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2008
Jacqueline C Escobar Piccoli Maria Gabriela Valle Gottlieb Luciano Castro Luiz Carlos Bodanese Euler Roberto Fernandes Manenti Mauricio Reis Bogo Alessandra Peres Maria Izabel U M da Rocha Ivana Beatrice Mânica da Cruz

Metabolic syndrome (MS) is a cluster of cardiovascular risk factors such as hypertension, dyslipidemia, obesity and type II diabetes. Here, we performed a case-control study analyzing the association between 894G>T endothelial nitric oxide synthase gene polymorphism (NOS3) and MS in 616 subjects. Genotype frequencies were TT= 9.3%, GG= 37.2 and TG= 53.6% and the allelic frequencies were T=0.36 ...

2013
Boyi Yang Yuyan Liu Yongfang Li Shujun Fan Xueyuan Zhi Xiangxiang Lu Da Wang Quanmei Zheng Yinuo Wang Yanxun Wang Guifan Sun

BACKGROUND Methylenetetrahydrofolate reductase (MTHFR) C677T, A1298C and methionine synthase reductase (MTRR) A66G polymorphisms are important genetic determinants for homocysteine (Hcy) levels, and are associated with several disorders. These polymorphisms are heterogeneously distributed worldwide. Our objective was to explore the geographical distributions of these polymorphisms in China. M...

Journal: :Molecular vision 2006
Wenliang Yao Xiaodong Jiao J Fielding Hejtmancik M Cristina Leske Anselm Hennis Barbara Nemesure

PURPOSE To investigate whether single nucleotide polymorphisms (SNPs) in the OPA1 gene are associated with two primary open-angle glaucoma (POAG) subgroups: those with elevated intraocular pressure (POAG/IOP) and those with normal tension glaucoma (NTG) in the African-Caribbean population of Barbados, West Indies. METHODS SNPs at intervening sequence (IVS) 8, +4, and +32 of the OPA1 gene were...

2012
Ji-In Yu Weon-Cheol Han Ki-Jung Yun Hyung-Bae Moon Gyung-Jae Oh Soo-Cheon Chae

BACKGROUND Interleukin 31 (IL-31) is a T helper type 2 effector cytokine that plays an important role in the pathogenesis of atopic and allergic diseases. IL-31 may be involved in promoting allergic inflammation and in inducing airway epithelial responses such as allergic asthma. METHODS Single-base extension analysis was used to detect the genotypes of IL-31 single nucleotide polymorphisms (...

2016
Mohammad Waseem Syed Rizwan Hussain Shashank Kumar Mohammad Serajuddin Farzana Mahdi Satyendra Kumar Sonkar Cherry Bansal Mohammad Kaleem Ahmad

BACKGROUND Breast cancer is one of the most common malignancies in women and is associated with a variety of risk factors. The functional single-nucleotide polymorphism (SNP) C677T in the gene encoding 5,10-methylenetetrahydrofolate reductase (MTHFR) may lead to decreased enzyme activity and affect the chemosensitivity of tumor cells. This study was designed to investigate the association of MT...

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