نتایج جستجو برای: fxiiival34leu polymorphism

تعداد نتایج: 107343  

Journal: :genetics in the 3rd millennium 0
hamed sharifinejad mohammad bagher montazer torbati homayoun farhangfar

ghrelin is a peptide hormone that is composed of 26 amino acids and leads to a positive energy balance and obesity through stimulation of releasing growth hormone, and increasing food intake and body weight.  the purpose of this study was to determine and evaluate the association between the ghrelin gene polymorphism and growth traits in ross and cobb broiler chickens. blood samples were collec...

Journal: :بینا 0
طاهره محمدیان mohammadian university of tabriz, tabriz, iranدانشکده علوم طبیعی- دانشگاه تبریز- تچشم پزشکبریز- ایران مرتضی جبارپور بنیادی jabarpoor bonyadi university of tabrizدانشکده علوم طبیعی- دانشگاه علوم پزشکی تبریز و مرکز تحققات سلامت کودکان- دانشگاه علوم پزشکی تبریز- تبریز- ایران محمدحسین جبارپور بنیادی jabarpoor bonyadi university of tabrizقطب علمی تنوع زیستی- دانشگاه علوم پزشکی گناباد- گناباد- ایران حمید احمدیه ahmadieh university of tabrizمرکز تحقیقات چشم- دانشگاه شهید بهشتی- تهران- ایران زکیه یعقوبی yaghoobi university of tabrizدانشگاه علوم پزشکی گناباد- گناباد- ایران

purpose: to investigate the effect of ccl2c-2512t polymorphism on age-related macular degeneration (amd). methods: this study enrolled 48 patients originating from northeast of iran who suffered from dry type amd. the association of c-2518t in the promoter region of ccl2 gene was investigated using polymerase chain reaction (pcr) and restriction fragment length polymorphism (rflp). control grou...

Journal: :acta medica iranica 0
a nikzamir department of biochemistry, school of medicine, ahwaz jondi shapour university of medical sciences, m nakhjavani endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic t golmohammadi department of biochemistry, school of medicine, tehran university of medical sciences, tehran, iran l dibai endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic r saffary endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic

diabetes mellitus is a multifactorial disease. it has recently been shown that an insertion (i)/deletion (d) polymorphism exists in the angiotensin-converting enzyme (ace) gene that can affect the serum ace level. there are three genotypes: dd, di, and ii, with the ace level being highest in dd, intermediate in di, and lowest in ii. in the present investigation, 170 patients with type 2 diabete...

Journal: :jundishapur journal of microbiology 0
abbas behelgardi gastroenterology and liver diseases research center, research institute for gastroenterology and liver diseases, shahid beheshti university of medical sciences, tehran, ir iran; department of microbiology, faculty of biological sciences, shahid beheshti university, tehran, ir iran seyed masoud hosseini department of microbiology, faculty of biological sciences, shahid beheshti university, tehran, ir iran seyed reza mohebbi basic and molecular epidemiology of gastrointestinal disorders research center, research institute for gastroenterology and liver diseases, shahid beheshti university of medical sciences, tehran, ir iran; basic and molecular epidemiology of gastrointestinal disorders research center, research institute for gastroenterology and liver diseases, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122432515, fax: +98-2122432516 pedram azimzadeh gastroenterology and liver diseases research center, research institute for gastroenterology and liver diseases, shahid beheshti university of medical sciences, tehran, ir iran shaghayegh derakhshani gastroenterology and liver diseases research center, research institute for gastroenterology and liver diseases, shahid beheshti university of medical sciences, tehran, ir iran khatoon karimi foodborne and waterborne diseases research center, research institute for gastroenterology and liver diseases, shahid beheshti university of medical sciences, tehran, ir iran

background interleukin-16 (il-16) is an immunomodulatory cytokine, which plays an important role in some inflammatory and autoimmune diseases such as hepatitis b, which is a major health concern worldwide. objectives in this study, we aimed to investigate the plausible association between il-16 polymorphism and chronic hbv susceptibility in an iranian population. conclusions these findings show...

Journal: :international journal of reproductive biomedicine 0
shiva shahsavari zahra noormohammadi shohreh zare karizi

background: recurrent spontaneous abortion is one of the diseases that can lead to physical, psychological, and, economical problems for both individuals and society. recently a few numbers of genetic polymorphisms in kinase insert domain-containing receptor (kdr) gene are examined that can endanger the life of the fetus in pregnant women. objective: the risk of kdr gene polymorphisms was inves...

Introdution: Endometriosis is one of the most common gynecologic disorders and shows significantly elevated prevalence in industrial regions. Additionally, a possible genetic predisposition is assumed for the disease. Glutathione S-transferases (GSTs) are enzymes participated in the metabolism of many human disease-causing mutagens, carcinogens and environmental pollutants. A functionally signi...

Background and objectives: Gastric cancer is one of the most common cancers of the gastrointestinal tract in the world, which also has a high prevalence in Iran. ERCC2 gene is considered one of the major genes related to gastric cancer. The present study aimed to investigate the relationship between rs13181 polymorphism of ERCC2 gene. The polymorphism in the promoter region of ERCC2 gene can af...

Background and Aims: Ficolins are proteins that bind to carbohydrates, act as opsonins and play an important role in innate immunity. Polymorphism in ficolin-3 gene (FCN3) can lead to complement deficiency and increase the risk of some disorders such as diabetes. The aim of this study was to investigate the frequency of FCN3+1637delC as a single nucleotide polymorphism in this gene in healthy a...

ژورنال: مجله دندانپزشکی 2008
دیهیمی, پرویز, مرسلی, فرشته, نیکبخت دستجردی, مهدی, کاظمی, شادی,

Background and Aim: A single nucleotide polymorphism at codon 72 of the p53 gene alters the p53 protein structure and affects its activity. This polymorphism depends on geographic regions and race. Also its association with some cancers has been reported. The aim of this study was to investigate this polymorphism in well differentiated oral SCC and normal population in the city of Isfahan. Mat...

Background: Single nucleotide polymorphisms (SNPs) have been introduced as a new genomic source for cancer. Therefore, it was decided to conduct a study to evaluate the rs3746444 polymorphism of miR-499 in patients with colon cancer in comparison with healthy subjects. Methods: This case-control study was conducted to investigate rs3746444 polymorphism of miR-...

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