نتایج جستجو برای: mutation detection method

تعداد نتایج: 2333870  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز - دانشکده شیمی 1392

in the present work, a simple and sensitive method was developed for determination of morphine and heroin using gold nanoparticles as resonance rayleigh scattering (rrs) and colorimetric technique’s probe. synthesized gold nanoparticles by sodium citrate reduction method have a negative charge layer on their surfaces because of self-assembled citrate anions on their surface. binding of morphin...

Journal: :medical journal of islamic republic of iran 0
vahid yassaee shahid beheshti university of medical sciences, koodakyar st., daneshjoo blvd, velenjak ave., tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) a dalton north trent molecular genetics service, sheffield children’s hospital, western bank, sheffield - s102th, ukسازمان اصلی تایید شده: 0 دانشگاه های خارج از کشور

abstract background: many disease susceptibility genes are large and consist of many exons in which point mutations are scattered throughout. scanning each exon individually represents a tedious task which can be time consuming and expensive. there has been increasing demand for rapid and accurate methods for full scanning of unknown point mutations in large multi-exon genes. gene assembling is...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز - دانشکده علوم پایه 1391

a simple, rapid and low-cost scanner spectroscopy method for the glucose determination by utilizing glucose oxidase and cdte/tga quantum dots as chromoionophore has been described. the detection was based on the combination of the glucose enzymatic reaction and the quenching effect of h2o2 on the cdte quantum dots (qds) photoluminescence.in this study glucose was determined by utilizing glucose...

پایان نامه :دانشگاه آزاد اسلامی - دانشگاه آزاد اسلامی واحد یزد - دانشکده شیمی 1392

in this study, a simple, rapid and selective method was developed for the determination of dexamethasone. the proposed method is based on inhibitory effect of dexamethasone on the oxidation of orange-g by bromate in sulfuric acid media. the reaction was followed spectrophotometrically at 478.5 nm (?max). under optimum experimental conditions, (72.6 ?mol l-1 of orange-g, 0.76 mol l-1 of h2so4, 0...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه صنعت آب و برق (شهید عباسپور) - دانشکده مهندسی برق و کامپیوتر 1392

abstract according to increase in electricity consumption in one hand and power systemsreliability importance in another , fault location detection techniqueshave beenrecentlytaken to consideration. an algorithm based on collected data from both transmission line endsproposed in this thesis. in order to reducecapacitance effects of transmission line, distributed parametersof transmission line...

Background & Objective: FLT3-ITD mutation detection has been an integral part of diagnostic work ups focused on acute myeloid leukemia. However, some studies have indicated that the mutation is unstable during the various stages of the disease. The purpose of this study was to evaluate the stability of this marker in paired diagnosis-relapse samples using Delta-PCR method. Materials & Methods:...

Journal: :journal of family and reproductive health 0
mina izadyar children medical center, medical sciences/ university of tehran, tehran, iran jila dastan gene clinic, tehran, iran tayebeh sabokbar department of genetics and genomics, cancer research center, tehran, iran solmaz shoraka department of genetics and genomics, cancer research center, tehran, iran azadeh shojaei vali-e-asr reproductive health research center, medical sciences /university of tehran, iran habib nasiri department of medical genetics, medical sciences /university of tehran, iran

objective: this study was designed to investigate rbc indices and hba2 levels in parents of major beta-thalassemia patients to detect possible silent beta- thalassemia carriers and examine its potential impact on the premarital genetic counseling. materials and methods: this cross sectional study was performed at children medical center from 2004 to 2006. after genetic counseling and getting in...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علامه طباطبایی - دانشکده اقتصاد 1393

due to extraordinary large amount of information and daily sharp increasing claimant for ui benefits and because of serious constraint of financial barriers, the importance of handling fraud detection in order to discover, control and predict fraudulent claims is inevitable. we use the most appropriate data mining methodology, methods, techniques and tools to extract knowledge or insights from ...

Journal: :iranian journal of basic medical sciences 0
nahid karimian fathi medical genetic department medical faculty, tabriz university of medical sciences, tabriz, iran mahmood shekari khaniani medical genetic department medical faculty, tabriz university of medical sciences, tabriz, iran vahid montazeri general surgery department medical faculty, tabriz university of medical sciences, tabriz, iran sima mansoori derakhshan medical genetic department medical faculty, tabriz university of medical sciences, tabriz, iran

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 (e...

Journal: :iranian journal of child neurology 0
massoud houshmand assistant professor of human genetics, genetic department of special medical center & national institute for genetic engineering and biotechnology,medical genetic dep, tehran, iran omid aryani genetic counselor, special medical center, genetic diagnostic laboratory, tehran, iran zahra pirzadeh assistant professor of pediatric neurology, qazvin university of medical sciences, qazvin, iran fereshteh ghasemi genetic technician, special medical center, tehran, iran shadab salehpour freshteh tehrani

glutaric acidemia, type i (ga i), was first described in 1975. the disease is caused by a genetic deficiency of the enzyme, glutaryl-coa dehydrogenase (gcd), which leads to the buildup of glutaric acid in the tissues and its excretion in the urine of affected patients. gcd is involved in the catabolism of the amino acids, lysine, hydroxylysine, and tryptophan. over 200 cases of ga i have been r...

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