نتایج جستجو برای: tetra arms

تعداد نتایج: 35748  

Background and Aim: Coronary artery disease (CAD) is a multifactorial inherited disorder in which the arteries that blood to the heart muscle become hardened and narrowed. We aimed at investigating the role of rs5186 (A1166C) polymorphism the angiotensin II type 1 receptor (AGTR1) gene as risk factors in some Iranian CAD patients. Materials and Methods: In this case-control study 137 samples...

Journal: :Agronomy 2022

Sugarcane is an important sugar and energy crop in the world. Germplasm innovation a significant way to breed breakthrough sugarcane varieties. Modern varieties all contain blood relationship of Saccharum officinarum spontaneum. High results from S. resistance genes In order improve quality, breeders use spontaneum cross obtain hybrid offspring with high resistance. Therefore, authenticity prog...

Journal: :international journal of molecular and cellular medicine 0
mohammad naderi research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) mohammad hashemi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) parisa khorgami research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) maliheh koshki research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) mahboubeh ebrahimi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) shadi amininia department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences)

single-nucleotide polymorphisms (snps) in mirnasmay alter its expression levels or processing and contribute to susceptibility to a wide range of diseases. our study aimed to evaluate the possible association between mirna-146a rs2910164 and mirna-499 rs3746444 polymorphisms and susceptibility to pulmonary tuberculosis (ptb) in a sample of iranian population. this case- control study was perfor...

Journal: :Genetics and molecular research : GMR 2010
R Marquis-Nicholson E Glamuzina D Prosser C Wilson D R Love

We developed a mutation-screening protocol for the ASS1 gene in order to guide clinical management of neonates with elevated citrulline detected during routine newborn screening. An exon-based amplification and sequencing method was designed and successfully applied to patients to identify disease-associated mutations. The sequencing-based method was applied to three patients with mild or asymp...

ژورنال: یافته 2018

Background: Alzheimer's disease is a multi-factorial disorder. The genes involved in Alzheimer's disease act as risk factors. The aim of this study was to investigate the APOE gene polymorphism in patients with Alzheimer's disease in Iran. Materials and Methods: In this analytical-descriptive study, 50 patients with Alzheimer's were investigated. Polymorphism of the APOE gene was investigated ...

Type 2 diabetes mellitus is a worldwide epidemic disorder with considerable health and economic consequences. Metformin is one of the most commonly prescribed oral antidiabetic drugs. Pharmacogenetic studies showed that variants in genes related to the pharmacokinetics of metformin were associated with glucose-lowering effect of metformin. The aim of this study was to evaluate pharmacogenetic v...

Journal: :Advances in experimental medicine and biology 2005
Tamás Decsi Cristina Campoy Berthold Koletzko

In this placebo controlled, randomised, double blind trial, pregnant women received from the 20th week of gestation onwards either 500 mg docosahexaenoic acid (DHA), 400 mg 5-methyl-tetra-hydro-folate (5-MTHF), or placebo, or a combination of 500 mg DHA and 400 mg 5-MTHF. The dietary supplements were well tolerated; the dropout rates did not differ significantly in the active arms of the study ...

Journal: :iranian journal of basic medical sciences 0
tausif ahmed rajput department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan abdul khaliq naveed department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan shakir khan department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan zia-ur rehman farooqi department of biochemistry and molecular biology, centre for research in experimental and applied medicine (cream), army medical college, national university of sciences & technology (nust), islamabad, pakistan

objective(s):organic anion transporter polypeptide 1b1 (oatp1b1) encoded by solute carrier organic transporter 1b1 (slco1b1) gene; a transporter involved in the uptake of drugs and endogenous compounds is present in hepatocyte sinusoidal membrane. aim of this study was to investigate the frequencies of functionally significant snps (388a>g and 521t>c) and their haplotypes in 6 ethnic groups of ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه سیستان و بلوچستان - دانشکده علوم پایه 1392

پیش زمینه : دیابت نوع 2 یا دیابت بزرگسالان در میانسالی بروز می کند و زمینه ارثی در ایجاد آن دخیل است ،این نوع دیابت بدلیل مقاومت پیدا کردن سلول های بدن به انسولین رخ می دهد. ژن تیروزیناز (tyr ) کهروی کروموزوم شماره 11 وجود دارد از ژنهایی است که کمتر در بیماری دیابت مورد بررسی قرار گرفته است ، این ژن آنزیم تیروزیناز را کد می کند .هدف ما در این تحقیق ، شناسایی ارتباط احتمالی snp شماره 4987234rs ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه سیستان و بلوچستان - دانشکده علوم پایه 1392

پیش زمینه: مالتیپل اسکلروزیس(ms) یک بیماری التهابی سیستم اعصاب مرکزی می باشد که اغلب افراد جوان را تحت تاثیر قرار می دهد، سایتوکاین ها به عنوان واسطه های التهاب و میلین زدایی نقش مهمی در بروز بیماری ms ایفا می کنند، هدف از مطالعه ی حاضر بررسی ارتباط پلی مورفیسم ژن های اینترلوکین 19 و 20 با بیماری ms در نمونه های تهیه شده از استان سیستان و بلوچستان می باشد. مواد و روش ها : در این تحقیق که یک مط...

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