نتایج جستجو برای: gene polymorphism

تعداد نتایج: 1185940  

Journal: : 2022

Identification of Polymorphism Melanocortin 4 Receptor Gene and its Association with Egg Production Traits in Turkey

Background The tumor necrosis factor alpha (TNF-α) gene is a cytokine involved in systemic inflammation. Results of the association of its polymorphisms with infertility in men are controversial.  Objective The aim of this study was to evaluate the association of -308G/A polymorphism in TNF-α gene with different parameters of semen and sperm in infertile men.  Methods Participants were 210 me...

Journal: : 2021

Association Between β-Defensin Gene Polymorphism and Clinical Mastitis in Holstein Dairy Cows: A Case-Control Study

Journal: :iranian journal of applied animal science 2014
d.s. kale b.r. yadav j. prasad

dna polymorphism within diacylglycerol transferase 2 (dgat2) / monoacyl glycerol transferases 2 (mogat2), leptin and butyrophilin genes were analysed using pcr-sscp in murrah buffalo. the single strand conformation polymorphism (sscp) analysis of amplified gene fragment in exon 5 of mogat2, exon 3 of leptin and intron 1 of butyrophilin gene revealed different patterns. a, b and c showed the fol...

حاتمی, یاسین, روانشاد, مهرداد, زالی, محمدرضا, صالحی, مجتبی, عظیم زاده, پدرام, محبی, سید رضا, کارخانه, مریم, کشاورز پاک سرشت, بهتا,

Background and purpose: Cytokines are a group of endogenous proteins which play an influential role in regulating the inflammatory responses and defeating infectious diseases. Elevated levels of proinflammatory cytokines and their receptors are usually observed in association with immune responses against viral infections such as hepatitis B virus (HBV) infection. IL 12 and its receptor play an...

ژورنال: Hormozgan Medical Journal 2013
Fatemi, R. , Karimi, K. , Safaei, A. , Zali, M.R. , Arkani, M. , Mohebi, R. , Vafaei, M. , Vahedi, M. ,

Introduction: Studies show polymorphism in leptin gene cause increase in level of leptin hormone and increased level of leptin hormon is associated with abosity, insulin resistance and increased risk of colorectal cancer. The aim of this study was to assess the incidence of leptin gene polymorphism rs 7799039 in Tehran and to investigate the influence of this polymorphism in increased risk of c...

Journal: :journal of family and reproductive health 0
mohammad karimian gametogenesis research center, kashan university of medical sciences, kashan, iran hossein nikzad gametogenesis research center, kashan university of medical sciences, kashan, iran abolfazl azami-tameh anatomical sciences research center, kashan university of medical sciences, kashan, iran aliakbar taherian gametogenesis research center, kashan university of medical sciences, kashan, iran fatemeh zahra darvishi department of biology, division of biochemistry, cell and molecular biology, university of isfahan, isfahan, iran mohammad javad haghighatnia gametogenesis research center, kashan university of medical sciences, kashan, iran

objective: to investigate the association of c631t single nucleotide polymorphisms in spo11 gene with male infertilityfollowed by an in silico approach. spo11 is a gene involved in meiosis and spermatogenesis process, which in humans, this gene is located on chromosome 20 (20q13.2-13.3) with 13 exons. materials and methods: in a case-control study, 200 blood samples were collected from the ivf ...

Journal: :iranian journal of allergy, asthma and immunology 0
ali talaei psychiatry and behavioral sciences research center, mashhad university of medical sciences, mashhad, iran jalil tavakkol afshari immunology research center, mashhad university of medical sciences, mashhad, iran mohammad reza fayyazi bordbar psychiatry and behavioral sciences research center, mashhad university of medical sciences, mashhad, iran hamidreza pouryousof psychiatry and behavioral sciences research center, mashhad university of medical sciences, mashhad, iran farhad faridhosseini psychiatry and behavioral sciences research center, mashhad university of medical sciences, mashhad, iran ali saghebi psychiatry and behavioral sciences research center, mashhad university of medical sciences, mashhad, iran

the pathogenesis of bipolar i disorder (bp-i) involves immune-mediated mechanisms, especially an imbalance in pro-inflammatory/anti-inflammatory cytokines in plasma or cerebrospinal fluid. interleukin-1 (il-1) gene cluster, coding some of these pro-inflammatory cytokines, might play a role in various neuropathologies related to neuron inflammation. the aim of the present study was to investigat...

Journal: :iranian journal of allergy, asthma and immunology 0
houshang rafatpanah reza farid gelareh golanbar farahzad jabbari azad

although the structure of human t lymphoptropic virus type i (htlv-i) has been known well, the function of some proteins encoded by htlv-i px region is not fully understood. furthermore, the responses of the immune system to htlv-i remain still unknown. most of htlv-i-infected individuals show a strong and persistently activated cytotoxic t-cell (ctl) response to the virus. the frequency of htl...

Journal: :physiology and pharmacology 0
pedram torabian student research committee, golestan university of medical sciences, gorgan, iran ayyoob khosravi student research committee, golestan university of medical sciences, gorgan, iran mehdi gholizadeh student research committee, golestan university of medical sciences, gorgan, iran mehdi zahedi ischemic disorders research center, golestan university of medical sciences, gorgan, iran majid haghjoo shahid rajaei cardiovascular, medical and research center echocardiography research center, tehran university of medical sciences, tehran, iran morteza oladnabi department of human genetics, school of advanced technologies in medicine, golestan university of medical sciences, gorgan, iran

introduction: congenital long qt syndrome (lqts) is a cardiac disorder characterized by qt interval prolongation at basal ecg. different lqts genes encode ion channel subunits or proteins involved in regulating cardiac ionic currents. long qt syndrome type 6 (lqt6) is caused by mutation in the kcne2 gene. our research aimed to analyze genetic variants of kcne2 gene causing the disease in irania...

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