نتایج جستجو برای: setx gene

تعداد نتایج: 1141403  

Journal: :iranian journal of biotechnology 2006
alireza zebarjadi

the biosynthetic pathways of saturated and unsaturated fatty acids consist of many steps controlled by various enzymes. one of the methods for improving oil quality is to change the fatty acid profile through genetic manipulation which requires isolation and characterization of the genes and other cis-acting elements, such as the promoter, involved in fatty acid biosynthesis. b-ketoacyl-coa syn...

Journal: :international journal of molecular and cellular medicine 0
majid mojarad department medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) mohammad hassanzadeh-nazarabad medical genetics research center, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) niaiesh tafazoli department medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

implantation failure is the most frequent cause of pregnancy loss in couples who try to conceive, either in a natural way or using assisted reproductive techniques (art). identify the precise mechanisms of implantation failure can lead to identify couples at risk and also providing appropriate therapeutic options to affected couples. despite the high prevalence of this disorder, a few causing f...

Journal: :iranian journal of pharmaceutical research 0
mehrdad hashemi associate of prod.,departmaent of genetics,iau,tehran medical branch

background & target: ischemia reperfusion injury is the tissue damage caused when blood supply returns to the tissue after a period of ischemia or lack of oxygen. in this study, the effect of pentoxyfylline on bcl2 gene expression changes and cell injury in kidney of rat following ischemia reperfusion were evaluated.methods: in this experimental study, 20 male wistar rats with average weight of...

Journal: :international journal of hematology-oncology and stem cell research 0
z rahimi medical biology research center, kermanshah university of medical sciences, kermanshah, iran. biochemistry department, medical school, kermanshah university of medical sciences, kermanshah, iran a merat biochemistry department, medical school, shiraz university of medical sciences, shiraz, iran m akhzari biochemistry department, medical school, shiraz university of medical sciences, shiraz, iran m haghshenass hematology research center, shiraz university of medical sciences, shiraz, iran nagel ronald l department of medicine, division of hematology; department of physiology and biophysics, albert einstein college of medicine, bronx, ny, usa gerard nathalie nserm u763, hôpital robert debrè, paris, france

introduction: β-globin gene cluster haplotypes are useful in diagnosis of particular molecular defects in β-thalassemia, prenatal diagnosis of β-thalassemia, and elucidating population affinities. methods: β-globin gene cluster haplotypes were studied in 150 β-thalassemia minor and 52 healthy in-dividuals from the fars province of iran. dna was extracted from leukocytes of whole blood by phe-no...

Journal: :iranian journal of public health 0
ar meamar m rezaian s rezaie m mohraz m mohebali k mohammad

cryptosporidium is an apicomplexan parasite of humans and a wild range of domestic as well as wild animals. an 833-bp fragment of the 18s-rrna gene was used to identify cryptosporidium spp. recovered from children and adult patients, in human immunodeficiency virus (hiv) positive and negative patients in iran. initial identification of cryptosporidiosis was carried out by ziehl-neelsen acid-fas...

Journal: :iranian journal of immunology 0
ali akbar amirzargar immunogenetic lab. dep. of immunology, school of medicine, tehran university of medical sciences, tehran, iran morteza bagheri department of sciences, university of khatam, tehran, iran ardeshir ghavamzadeh hematology- oncology and bmt research center, shariati hospital, tehran, iran kamran alimoghadam hematology- oncology and bmt research center, shariati hospital, tehran, iran farideh khosravi immunogenetic lab. dep. of immunology, school of medicine, tehran university of medical sciences, tehran, iran mohammad hossein nicknam immunogenetic lab. dep. of immunology, school of medicine, tehran university of medical sciences, tehran, iran mandana moheydin

background:it has been hypothesized that genetic factors other than histocompatibility disparity may play a role in predisposition to developing chronic myelogenous leukemia (cml). in this regard, th1 and th2 cytokines and their gene polymorphism seems to be important. overall expression and secretion of cytokines is dependent, at least in part, on genetic polymorphism (nucleotide variations) w...

Journal: :international journal of reproductive biomedicine 0
nasrin majidi gharenaz mansoureh movahedin zohreh mazaheri shahram pour beiranvand

background: nowadays, oocytes and embryos vitrification has become a routine technique. based on clinical judgment, re-vitrification maybe required. but little is known about re-vitrification impact on genes expression. objective: the impact of re-vitrification on apoptotic and implanting genes, bax, bcl-2 and erbb4, at compaction stage embryos were evaluated in this study. materials and method...

2015
Mário J.J. Branco Gracinda M.S. Gomes Victoria Gould

Ehresmann monoids form a variety of biunary monoids, that is, monoids equipped with two basic unary operations, the images of which coincide and form a semilattice of projections. The monoid of binary relations BX on any setX with unary operations of domain and range is Ehresmann. Inverse monoids, regarded as biunary submonoids of BX via the Wagner-Preston representation theorem, are therefore ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - پژوهشگاه ملی مهندسی ژنتیک وزیست فناوری 1389

ژن درمانی با استفاده از روش هدف گیری ژنی (gene targeting) یکی از بهترین روشهای درمان نقائص ژنتیکی نظیر بتا تالاسمی می باشد. بیماری بتا تالاسمی در اثر کاهش یا فقدان سنتز زنجیره بتا گلوبین به وجود می آید. یکی از روشهای درمان موثر برای این بیماری ژن درمانی توسط حامل های لنتی ویروسی می باشد. ظرفیت حامل های لنتی ویروس حدود 10 کیلو باز است. هدف از این تحقیق طراحی و ساخت حامل لنتی ویروس های نوترکیب فا...

Journal: :physiology and pharmacology 0
olga yu. fedorenko mental health research institute, tomsk nrmc, russia anton j.m. loonen department of pharmacy, university of groningen, groningen, the netherlands natalya m. vyalova mental health research institute, tomsk nrmc, russia аnastasiya s. boiko mental health research institute, tomsk nrmc, russia ivan v. pozhidaev mental health research institute, tomsk nrmc, russia diana z. osmanova mental health research institute, tomsk nrmc, russia

introduction: hyperprolactinemia is a common serious side effect of antipsychotic medications that are currently used in the treatment of patients with schizophrenia. pharmacogenetic approaches offer the possibility of identifying patient-specific biomarkers for predicting the risk of this side effect. we investigated a possible relationship between variants (snps) in genes for cytochrome 2d6 (...

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