نتایج جستجو برای: gene polymorphism

تعداد نتایج: 1185940  

بوالحسنی, اعظم, حبیب, اسدالله, نصیری, محبوبه, کهن, لیلا,

Introduction: Leptin, the obese (ob) gene product, is a cytokine-like hormone secreted mainly from adipose tissue acting on a receptor site in the hypothalamus to inhibit food intake and stimulate energy expenditure. A G-2548G polymorphism in the leptin gene promoter has a strong influence on leptin gene expression and adipose tissue secretion. The aim of this study was to examine the associati...

Background and purpose: Chronic lymphocytic leukemia (CLL) is the most common form of adult leukemia characterized by the accumulation of seemingly mature type B lymphocytes in peripheral blood and lymphatic organs. One of the main markers used in the diagnosis and prognosis of CLL is the CD38 gene. Polymorphism is considered to be a major genetic source of phenotypic change within a species an...

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 ...

Journal: :cell journal 0

objective: people are usually susceptible to carcinogenic aromatic amines, present in cigarrette smoke and polluted environment, which can cause dna damage. therefore, maintenance of genomic dna integrity is a direct result of proper function of dna repair enzymes. polymorphic diversity could affect the function of repair enzymes and thus augment the risk of different cancers. xeroderma pigment...

Journal: :iranian journal of medical sciences 0
s.h. jahadi-hossieni organ transplant rearch center, namazee hospital shiraz university of medical sciences shiraz iran. e. kamali department of immunology school of medicine namazee hospital shiraz university of medical sciences shiraz iran m. samani department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran a. katbab department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran h. khoshniat department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran h. movahhedan department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran

background: correlations between bone marrow, heart, kidney, liver, skin and lung transplant rejection or survival with human cytokine gene polymorphisms have been described. there are also reports about the role of cytokines and tumor necrosis factors-alpha (tnf-α) on corneal transplant in animal models. further studies are needed to clarify the role of cytokines in corneal allograft rejection...

The present study was carried out to investigate the association of C/T single nucleotide polymorphism(SNP)in exon 5 of stearoyl-CoA desaturase 1 (SCD1) gene and A/C SNP in the 3' untranslated region of oxidized low density lipoprotein receptor 1 (OLR1)gene with milk production traits in Iranian Holstein dairy Cattle. The blood samples of 153 (for OLR1) and 308 (for SCD1) dairy cattle from thre...

Journal: :Czech Journal of Animal Science 2021

Molecular cloning, functional characterization, tissue expression and polymorphism analysis of buffalo PRDX6 gene | Yongwang Miao, Lihua Qiu, Xinyang Fan, Xiaohong Teng, Pei Wang Agricultural Journals

Journal: :iranian journal of public health 0
saeedeh salimi cellular and molecular research center, zahedan university of medical sciences, zahedan, iran and dept. of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, iran. alireza nakhaee cellular and molecular research center, zahedan university of medical sciences, zahedan, iran and dept. of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, iran. mehdi jafari cellular and molecular research center, zahedan university of medical sciences, zahedan, iran. danial jahantigh dept. of internal medicine, school of medicine, zahedan university of medical sciences, zahedan, iran. mahnaz sandooghi dept. of internal medicine, school of medicine, zahedan university of medical sciences, zahedan, iran. zahra zakeri dept. of internal medicine, school of medicine, zahedan university of medical sciences, zahedan, iran.

background : progression of systemic lupus erythematosus (sle) could be due to oxidative stress especially through reactive oxygen species (ros). detoxification of ros is largely performed by glutathione s-transferases (gsts), therefore polymorphisms of gstm1, gstt1 and gstp1 genes which decrease enzymes activity could affect sle susceptibility. the aim of this study was to determine the effect...

Journal: :medical journal of islamic republic of iran 0
ali mohammad foroughmand dept of genetics, college of sciences, shahid chamran university, ahvaz,iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) maryam haidari dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) hamid galehdari dept of genetics, college of sciences, shahid chamran university, ahvaz-iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) atefeh pooryasin dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) seyed reza kazeminejad dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) shiva hosseini dept of genetics, college of sciences, shahid chamran university, ahvaz, iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university)

abstract   background: the disrupted-in-schizophrenia 1 (disc1) gene, on the chromosome position 1q42, was initially identified at the breakpoint of a balanced translocation, t(1,11)(q42.1q14.3), which segregated with major mental disorders in a large scottish family.   methods: our samples included 200 unrelated patients diagnosed with schizophrenia on the basis of dsm-iv criteria and 200 norm...

Journal: :iranian biomedical journal 0
مریم آیت الهی maryam ayatollahi احمد مرات ahmad merat منصور حق شناس mansour haghshenas

the restriction enzyme ava ii detects the base change of the intervening sequence ii (ivs ii) which is used as one of the markers of β-globin gene polymorphism. this study was conducted to determine the frequency of the ava ii site on the β-globin gene among normal people and patients with sickle cell syndrome (scs) in iran. dna fragments containing the ivs ii region of the β-globin gene from 3...

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