نتایج جستجو برای: frequency of allele

تعداد نتایج: 21194166  

Journal: :journal of research in medical sciences 0
hamid mirmohammad sadeghi associate professor, isfahan pharmaceutical sciences research center, isfahan university of medical sciences, isfahan, iran ali mohammad sabzghabaee associate professor, isfahan clinical toxicology research center, isfahan university of medical sciences, isfahan, iran zeinab mousavian pharmacy student, school of pharmacy, isfahan university of medical sciences, isfahan, iran mohammad saadatnia associate professor, department of neurology, school of medicine, isfahan university of medical sciences, isfahan, iran shahin shirani assistant professor, department of cardiology, school of medicine, isfahan university of medical sciences, isfahan, iran fatemeh moazzen research assistant, department of pharmaceutical biotechnology, school of pharmacy, isfahan university of medical sciences, isfahan, iran

background : apolipoprotein e (apoe) gene encodes an important protein in reforming injuries of central nervous system (cns). it is assumed that various apoe alleles may be functionally different. the purpose of this study was to investigate the distribution of apoe genotypes in multiple sclerosis (ms) patients in a small cohort of iranians. methods : in this case-control study, blood samples o...

Asadpor U Gourabi H Haghighat S Moazenchi M, Mohseni Meybodi A Sadighi Gilani MA Salman Yazdi R, Totonchi M

Background: Chlamydia trachomatis(CT) is an obligate intracellular bacteria, requires living cells to replicate itself. CT infection can remain up to 4 years in the couple and affect their fertility. The relationship between CT and infertility is very important because most patients are asymptomatic and untreated. After infection with CT, NK activation signals begin through interactions of its ...

Objective(s): FOXP3 gene is an X-linked gene that encodes FOXP3 protein, an essential transcription factor in CD4+CD25+FOXP3+ regulatory T (Treg) cells.  We aimed, in the present study, to investigate the association of two FOXP3 polymorphisms, -2383 C/T (rs3761549) and IVS9+459 T/C (rs2280883), with lung cancer. Materials and Methods:  In a case-control study we analyzed genotypes and alleles ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه گیلان - دانشکده علوم انسانی 1391

the present study sought to investigate the impact of using mind-mapping technique instruction on female elementary efl learners reading comprehension; it also investigated their attitudes towards using mind-mapping technique as a tool to improve their reading comprehension. this study followed a quasi-experimental design with two intact groups as experimental, and control groups. the participa...

ژورنال: Hormozgan Medical Journal 2013
Fatemi, R. , Karimi, K. , Safaei, A. , Zali, M.R. , Arkani, M. , Mohebi, R. , Vafaei, M. , Vahedi, M. ,

Introduction: Studies show polymorphism in leptin gene cause increase in level of leptin hormone and increased level of leptin hormon is associated with abosity, insulin resistance and increased risk of colorectal cancer. The aim of this study was to assess the incidence of leptin gene polymorphism rs 7799039 in Tehran and to investigate the influence of this polymorphism in increased risk of c...

Journal: :molecular biology research communications 0
zohreh rahimi medical biology research center, kermanshah university of medical sciences, kermanshah, iran hamed abdi department of clinical biochemistry, medical school, kermanshah university of medical sciences, kermanshah, iran maryam tanhapoor department of clinical biochemistry, medical school, kermanshah university of medical sciences, kermanshah, iran ziba rahimi medical biology research center, kermanshah university of medical sciences, kermanshah, iran asad vaisi-raygani department of clinical biochemistry, medical school, kermanshah university of medical sciences, kermanshah, iran hamid nomani department of clinical biochemistry, medical school, kermanshah university of medical sciences, kermanshah, iran

the variants of angiotensin converting enzyme (ace) and matrix metalloproteinases (mmps) genes might be involved in the pathogenesis of end stage renal disease (esrd) and hypertension. we studied the ace insertion/deletion (i/d) and mmp-7 a-181g variants in 99 unrelated esrd patients and 117 individuals without renal complications from western iran with kurdish ethnic background. the frequency ...

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