نتایج جستجو برای: Azeri Turkish

تعداد نتایج: 20399  

The subject intended to study the general methods of natural word-forming in Azeri Turkish language. This study aimed to reach this purpose by analyzing the construction of compound Azeri Turkish words. Same’ei (2016) did a comprehensive study on word-forming process in Farsi, which was the inspiration source of this study for Azeri Turkish language word-forming. Numerous scholars had done vari...

Journal: : 2023

This paper explores qoşma, postposition in modern Azeri and its Turkish counterpart. According to the common view on Azeri, postposition, particle, conjunctions, modals, interjection are listed under minor parts of speech. In grammar, there is a tendency categorize all speech single heading edat (particle), which results confusion about definition function particle. Words like particles conjunc...

Journal: :Genetic testing and molecular biomarkers 2010
Mortaza Bonyadi Mohsen Esmaeili Abbas Karimi Saeed Dastgiri

Familial Mediterranean fever (FMF) is an autosomal recessive disorder primarily affecting the Mediterranean populations. It is characterized by recurrent attacks of fever and inflammation of serosal membranes and gradual development of nephropathic amyloidosis. More than 70 disease-associated mutations have been identified in the Mediterranean fever gene (MEFV) responsible for FMF. The aim of t...

Journal: :Clinical genetics 2009
M Bonyadi M Esmaeili H Jalali M H Somi A Ghaffari M Rafeey K Sakha N Lotfalizadeh A Pourhassan M Khoshbaten M R Ardalan N Laghaeian

Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disorder with more than 60 disease-associated mutations in the responsible gene, MEFV. In the present study, we determined 15 MEFV mutations in Iranian Azeri Turkish FMF patients. Five hundred and twenty-four unrelated patients were tested for 15 known mutations in the MEFV gene using amplification refractory mutation...

Journal: :molecular and biochemical diagnosis (journal) 2014
mortaza bonyadi elahe nabat mahnaz sadeghi shabestari mandana rafeey fakhrossadat mortazavi

background: henoch-schönlein purpura (hsp) is an lga mediated small vessel systemic vasculitis disease in children. the etiology and pathogenesis of hsp disease remain unknown. however, environmental and genetic risk factors could play important roles in susceptibility to hsp disease. in this study we investigated the association of 5՛-untranslated region polymorphism (-634g/c) of vegf gene wit...

Journal: :Seminars in arthritis and rheumatism 2008
Mohsen Esmaeili Mortaza Bonyadi Mandana Rafeey Kazem Sakha Mohammad Hossein Somi

OBJECTIVES To identify the frequency and distribution of familial Mediterranean fever (FMF) gene (MEFV) mutations among Azeri Turkish patients from northwestern Iran. METHODS One hundred ninety unrelated patients were referred by specialists to the Molecular-Medical Genetic Center of Tabriz. A clinical diagnosis of FMF was made according to published criteria. Mutation screening of the MEFV g...

Esmail Faghih Masumeh Bahman

Thematisationis one of the troublesome areas both for translation purposes from or into English and also for learning EFL. The main reason for the problem lies in the fact that usually different languages structure thematisation in different ways. Therefore, the present research is an attempt to investigate contrastively: experiential (topical), interpersonal and textual themes in a sample of A...

2015

© 2015 The Authors; Tabriz University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Prevalence of the MEFV gene mutations and their clinical correlati...

Mahdieh Younesi Mohammadali HosseinpourFeizi, Nasser Pouladi

Background: Due to the lack of information about the role of 4G/5G polymorphism of PAI-1 Gene in susceptibility to thyroid tumors, this study was performed to evaluate the potential effects of this polymorphism on clinicopathologic features of thyroid tumors in Iranian Azeri Turkish patients. Methods:In this case-control study, 90 patients with thyroid tumors ...

2014
Nahid Karimian Fathi Mahmood Shekari Khaniani Vahid Montazeri Sima Mansoori Derakhshan

OBJECTIVE(S) Breast cancer is the most common cancer in women. Every year, one million new cases are reported worldwide, representing 18% of the total number of cancer in women. Hereditary BRCA1 and BRCA2 mutations account for about 60% of inherited breast cancer and are the only known causes of hereditary breast cancer syndrome. The aim of this study was to determine the frequency of BRCA2 (ex...

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