نتایج جستجو برای: scaleless gene

تعداد نتایج: 1141423  

Journal: :international journal of hematology-oncology and stem cell research 0
fatemeh farhid msc, department of hematology, school of allied medical sciences, tehran university of medical sciences, tehran, iran fatemeh nadali associate professor, department of hematology, school of allied medical sciences, tehran university of medical sciences, tehran, iran bahram chahardouli assistant professor, hematology-oncology and stem cell transplantation research center, tehran university of medical sciences, tehran, iran saeed mohammadi phd, hematology-oncology and stem cell transplantation research center, tehran university of medical sciences, tehran, iran shahrbano rostami assistant professor, hematology-oncology and stem cell transplantation research center, tehran university of medical sciences, tehran, iran kamran alimoghaddam professor, hematology-oncology and stem cell transplantation research center, tehran university of medical sciences, tehran, iran

background : to determine the frequency of the single nucleotide polymorphism m287t in exon 9 of the as3mt gene in iranian population and to assess the difference in allele frequencies with other ethnicities. subjects and methods : genotyping analysis was performed on 150 healthy subjects using the pcr-rflp assay. we used chi-square analysis to check the deviation from hardy–weinberg equilibriu...

Journal: :archives of razi institute 2016
a.h. shooshtari s.a. pourbakhsh k. aghaiypour h. keivanfar h.r. varshovi

sheeppox virus (spv) and goatpox virus (gpv) belong to the capripoxvirus genus of poxviridae family. sheeppox and goatpox along with contagious ecthyma (ce) are endemic diseases in iran. capripox laboratory conformation based on virological and serological techniques are time consuming, laborious and most of them of low specificity, because of close antigenic relationship between capripoxvirus ...

Journal: :iranian journal of public health 0
ozra tabatabaei-malazy mehrnoosh khodaeian mahsa m amoli

obesity is currently considered as a serious global health problem which is influenced by environmental and genetic factors. association of genetic variants with obesity is widely scrutinized in recent years. the aim of this study was to evaluate present data on genetics of obesity in iranian population in a systematic review study. to obtain all related studies, google scholar, pubmed, and per...

Journal: :iranian biomedical journal 0
zahra shams mofarahe marefat ghaffari novin mina jafarabadi mojdeh salehnia mohsen noroozian nassim ghorbanmehr

background: ovarian tissue cryopreservation is an alternative strategy to preserve the fertility of women predicted to undergo premature ovarian failure. this study was designed to evaluate the expression of folliculogenesis-related genes, including factor in the germline alpha (figla), growth differentiation factor-9 (gdf-9), follicle-stimulating hormone receptor (fshr), and kit ligand after v...

Journal: :iranian journal of public health 0
s salimi m firoozrai i nourmohammadi m shabani a zavarehee a mohebbi

endo-derived nitric oxide (no) is synthesized from l-arginine by endothelium nitric oxide synthase (enos). since reduced no synthesis has been implicated in the development of coronary atherosclerosis; we hypothesized that polymorphisms of nos gene might be associated with increased susceptibility to this disorder and coronary artery disease (cad). we studied the 27 base pair tandem repeat poly...

Journal: :basic and clinical neuroscience 0
amin dinarvand science and research branch of islamic azad university, tehran, iran. ali goodarzi iranian national center for addiction studies, tehran university of medical sciences, tehran, iran. nasim vousooghi department of neuroscience, school of advanced technologies in medicine, tehran university of medical sciences, tehran, iran. mehrdad hashemi department of genetics, islamic azad university, tehran medical branch, tehran, iran rasoul dinarvand department of pharmacoeconomics and pharmaceutical administration, faculty of pharmacy, tehran university of medical sciences, tehran, iran. fahimeh ostadzadeh science and research branch of islamic azad university, tehran, iran.

introduction: association between single-nucleotide polymorphisms (snps) in mu opioid receptor gene and drug addiction has been shown in various studies. here, we have evaluated the existence of polymorphisms in exon 3 of this gene in iranian population and investigated the possible association between these mutations and opioid addiction.  methods: 79 opioid-dependent subjects (55 males, 24 fe...

Journal: :jundishapur journal of microbiology 0
mohammad dadook faculty of biological science, islamic azad university tehran north branch, tehran, ir iran sedigheh mehrabian faculty of biological science, islamic azad university tehran north branch, tehran, ir iran mitra salehi faculty of biological science, islamic azad university tehran north branch, tehran, ir iran saeed irian department of cell and molecular biology, faculty of biological sciences, kharazmi university, tehran, ir iran; department of cell and molecular biology, faculty of biological sciences, kharazmi university, tehran, ir iran. tel: +98-2188329220

conclusions: it was concluded that increasing the concentration of zinc in the agricultural soil is harmful to beneficial microorganisms and reduces the soil fertility. a 20-ppm zinc concentration in soil is suggested to be optimal. background: zinc is an essential micronutrient used in the form of zinc sulfate in fertilizers in the agriculture production system. nitrogen-fixing microorganisms ...

Objective(s): The aim of this study was to investigate the methylation status and mRNA expression levels of P15, death-associated protein kinase (DAPK), and suppressor of cytokine signaling-1 (SOCS1) genes in multiple myeloma (MM). Materials and Methods: The bone marrow samples of 54 MM patients were collected and the methylation status of the P15, DAPK, and SOCS1 gene promoter regions was dete...

Journal: :iranian red crescent medical journal 0
ramak badr department of genetics, faculty of science, science and research branch, islamic azad university, tehran, ir iran mehrdad hashemi department of genetics, tehran medical sciences branch, islamic azad university, tehran, ir iran; department of genetics, tehran medical sciences branch, islamic azad university, tehran, ir iran. tel: +98-2122006660, fax: +98- 22008049 gholamreza javadi department of genetics, faculty of science, science and research branch, islamic azad university, tehran, ir iran abolfazl movafagh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran reza mahdian biotechnology research center, molecular medicine department, pasteur institute of iran, tehran, ir iran

conclusions the analysis of the pro-apoptotic gene to anti-apoptotic gene expression ratio (bad /bcl-xl) confirmed that expression of the pro-apoptotic gene significantly decreased (p value ˂ 0.001) under the ischemia/reperfusion condition. in contrast, the expression of the anti-apoptotic gene increased after administration of fk-506 (p value ˂ 0.001). results the quantitative results of real-...

Journal: :medical journal of islamic republic of iran 0
seyed reza kazemi nezhad department of genetics, faculty of science, shahid chamran universityof ahvaz, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) fatemeh mosavi department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) ali akbar momen ahvaz jundishapur university of medical sciences, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences) hamid galehdari department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) gholamreza mohamadian genetic counseling centre, khuzestan welfare organization, ahvaz, iran.سازمان های دیگر: khuzestan welfare organization

background: spinal muscular atrophy (sma) is the second most common lethal autosomal recessive disease. it is a neuromuscular disorder caused by degenerative of lower motor neurons and occasionally bulbar neurons leading to progressive limb paralysis and muscular atrophy. the smn1 gene is recognized as a sma causing gene while naip has been characterized as a modifying factor for the clinical s...

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