نتایج جستجو برای: azeri turkish
تعداد نتایج: 20399 فیلتر نتایج به سال:
Promoter polymorphism of cytokine genes may lead to inter-individual differences in cytokine levels, therefore, polymorphisms may associate with susceptibility to infectious diseases. In this study, we investigated a possible association between interleukin-10 (IL-10) -1082A⁄G (rs1800896) and interferon (IFN)-gamma +874T/A (rs2430561) promoter polymorphisms and tuberculosis (TB) in the Azeri po...
OBJECTIVE Duchene and Becker Muscular Dystrophy (DMD/ BMD) are x-linked disorders that both are the result of heterogeneous mutations in the dystrophin gene. The frequency and distribution of dystrophin gene deletions in DMD/ BMD patients show different patterns among different populations. This study investigates the deletion rate, type, and distribution of this gene in the Azeri Turk populati...
Bilingual lexicon induction is the task of inducing word translations from monolingual corpora in two languages. In this paper we present the most comprehensive analysis of bilingual lexicon induction to date. We present experiments on a wide range of languages and data sizes. We examine translation into English from 25 foreign languages: Albanian, Azeri, Bengali, Bosnian, Bulgarian, Cebuano, G...
For more than four decades, the Greek Cypriots and Turkish Cypriots have been negotiating in an effort to find a solution to the Cyprus problem. The perspective, assumptions and hypotheses that underpin the respective approaches to the Cyprus problem disclose the general framework that renders understandable the impasse that has characterised the long history of negotiations on Cyprus. The Hels...
Background and Aim: MDM4, a negative regulator of the p53 tumor suppression pathway, has been demonstrated to be overexpressed in a variety of human cancers. Research has revealed that the rs4245739 A>C polymorphism of MDM4 in the 3′-untranslated region makes it a miR-191 target site, leading to lower MDM4 expression. This study aimed to detect if the rs4245739 single nucleotide polymorphism (S...
INTRODUCTION Depending on the response to standard steroid therapy, nephrotic syndrome it is classified to steroid-sensitive and steroid-resistant nephrotic syndrome (SRNS). Mutations in several genes including NPHS2 have been implicated in SRNS. Gene R229Q polymorphism (p.R229Q) of NPHS2 is associated with adolescent- or adult-onset SRNS in European and South American populations. We investiga...
OBJECTIVE Hereditary hearing impairment is a genetically heterogeneous disorder. In spite of this, mutations in the GJB2 gene, encoding connexin 26 (Cx26), are a major cause of nonsyndromic recessive hearing loss in many countries and are largely dependent on ethnic groups. The purpose of our study was to characterize the type and prevalence of GJB2 mutations among Azeri population of Iran. M...
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