نتایج جستجو برای: frequency of allele

تعداد نتایج: 21194166  

Background and Objective: Ecto-nucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is a class II membrane glycoprotein that binds to insulin α receptor and can interfere in insulin signaling pathway. Transcription factor-7-like 2 (TCF7L2) is a transcription factor which plays a critical role in pancreatic β cell activity. ENPP1 and TCF7L2 gene polymorphisms may have functional role in suscep...

Journal: :iranian journal of allergy, asthma and immunology 0
kiani zahra department of immunology, chabahar international university of medical sciences, chabahar, iran tavakkol-afshari jalil department of immunogenetic, bu-ali research center, mashhad university of medical sciences, mashhad hojjat hamed department of immunogenetic, bu-ali research center, mashhad university of medical sciences, mashhad arab hamid reza department of periodontology, mashhad university of medical sciences, mashhad, iran radvar mehrdad department of periodontology, mashhad university of medical sciences, mashhad, iran sadeghizadeh mehrdad department of molecular genetic, tariat modarres university, tehran, iran

adult periodontitis is a complex multifactorial disease whose etiology is not well defined. the pro-inflammatory and bone resorption properties of interleukine-1α (il-1α) strongly suggest a role for this cytokine in the pathogenesis of periodontal disease. eighty iranian adult patients with periodontitis and 80 iranian controls were investigated in this study. in this study we report that the f...

Borhani, Tahura Sadat , Fayyaz-Movaghar, Afshin , Kamel-Mirmostafaee, Mohammad Taghi ,

Background and Purpose: The identification of genetics risk factors of human diseases is very important. This study is conducted to model the allele frequencies (AFs) of Alzheimer’s disease. Materials and Methods: In this study, several candidate probability distributions are fitted on a data set of Alzheimer’s disease genetic risk factor. Unknown parameters of the considered dis...

Behnam Askari, esmat khaleqsefat, Hamid Soraya, Mohammad Khalaj-Kondori, Morteza Jabbarpour bonyadi,

Warfarin is a commonly-prescribed anticoagulant used to treat and prevent thromboembolic events. The requirement for varying doses of warfarin depends on genetic and environmental components. In this study, the frequency of two single-nucleotide polymorphic variants of the vitamin K epoxide reductase complex subunit 1 (VKORC1) gene (1173 C>T (rs9934438) and 3730 G>A (rs7294)) and its correlatio...

Background: Factor V Leiden, Prothrombin gene (G20210A) and MTHFR (C677T) polymorphism are the main biomarkers for evaluation of tendency for venous thromboembolism. We aimed to investigate the frequency of mutations in factor V Leiden, Prothrombin G20210A and MTHFR C677T and identify the genetic status for these mutations in patients with venous thrombosis. Methods: This study was carried out...

Journal: :iranian journal of applied animal science 2015
f. mohamadnejad-sangdehi g. rahimi-mianji m. safdari-shahroudi s.a. razavi-sheshdeh m. gholami

this study was performed to investigate two polymorphic sites from cyp19 gene (pvuii and mspi) and one polymorphic site from erα gene (snabi) in four cattle breeds including mazandarani, taleshi, sistani and simmental. in overall 278 samples for cyp19 and 206 samples for erα marker sites were genotyped using polymerase chain reactionsingle-strand conformation polymorphism (pcr-rflp) procedure. ...

Alireza Esmaeili, Mahmoud Mahmoudi, Maryam Rastin, Shahrzad Zamani Taghizadeh Rabe

Objective(s): The population in Iran is a genetic admixture of the ancestral Aryan and other populations neighboring Iran. Different ethnic groups in Iran show wide regional distributions for many human leukocyte antigen (HLA) alleles. Therefore, it is necessary and sensible to study the differences in HLA allele distribution in different area. We studied the HLA class I and II allele frequenci...

ژورنال: پژوهش در پزشکی 2005
فریدون عزیزی, , مریم السادات دانشپور, , مهدی هدایتی, ,

Background: The aim of this study was to examine whether the well established effect of the common TaqI polymorphism in CETP gene on HDL-C concentration could be explained by the recently identified -629A/C functional polymorphism in the promoter. Material and method: To examine the association between A allele and HDL-C level, 943 healthy subjects enrolled in TLGS study were selected, among w...

Background Attention deficit hyperactivity disorder (ADHD) is a common behavioral disorder that affects 8-12% of school-age children. Several environmental and genetic factors play a role in the etiology of this disease. One of the genetic factors involved is dopamine beta-hydroxylase (DBH) gene, which plays an essential role in catecholamine synthesis by converting dopamine into norepinephrine...

Journal: :modares journal of medical sciences: pathobiology 2011
arezou sayad mahdi zamani mohammad taghi akbari feridoon mostafavi anooshirvan kazemnejad

objective: survey of the influence of hla-drb1, -dqb1 alleles, genotypes and haplotypes on age at onset of type 1 diabetes (t1d) in an iranian population materials and methods: 105 iranian t1d patients of different ethnic group and 100 ethnically, age and sex matched individuals were selected from tehran's hospitals and hla-drb, -dqb typing was performed. according to the age at onset of t1d, ...

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