نتایج جستجو برای: single nucleotide poly morphism

تعداد نتایج: 1025175  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم انسانی 1387

در مطالعه حاضر دو پلی مرفیسم تک نوکلئوتیدی single nucleotide polymorphisms;(snps) در نواحی t129c در اگزون 1 و t1236c در اگزون 12 ، ژن mdr1 در 200 بیمار مصروع ایرانی ( شامل دو گروه بیماران مصروع مقاوم به دارودرمانی و بیماران مصروع پاسخ دهنده به درمان دارویی، هر گروه 100 نفر) در کنار 100 نفر سالم به روشrflp pcr- مورد بررسی و تعیین ژنوتیپ قرار گرفت و فراوانی ژنوتیپ و هاپلوتیپی در این سه دسته مقایس...

Journal: :Nucleic acids research 1990
M D Sheets S C Ogg M P Wickens

Three sequences in the vicinity of poly (A) addition sites are conserved among vertebrate mRNAs. We analyze the effects of single base changes in each position of AAUAAA and in the nucleotide to which poly (A) is added on 3' end formation in vitro. All 18 possible single base changes of the AAUAAA sequence greatly reduce addition of poly (A) to RNAs that end at the poly (A) addition site, and p...

Journal: :iranian journal of allergy, asthma and immunology 0
xia ke department of otorhinolaryngology, the first affiliated hospital of chongqing medical university, chongqing, china yinglin yang department of otorhinolaryngology, the first affiliated hospital of chongqing medical university, chongqing, china yang shen department of otorhinolaryngology, the first affiliated hospital of chongqing medical university, chongqing, china xiaoqiang wang department of otorhinolaryngology, the first affiliated hospital of chongqing medical university, chongqing, china suling hong department of otorhinolaryngology, the first affiliated hospital of chongqing medical university, chongqing, china

tumor necrosis factor alpha-inducible protein 3 (tnfaip3) gene polymorphisms have been reported to be associated with the susceptibility to several immune-related diseases. here we investigated the effect of tnfaip3 gene polymorphisms on the risk of allergic rhinitis (ar) in a chinese han population. the case-control study included 540 ar patients and 524 healthy controls. genotyping for tnfaip...

Journal: :iranian journal of allergy, asthma and immunology 0
mahdi mahmoudi molecular immunology research center, tehran university of medical sciences, tehran, iran and rheumatology research center, shariati hospital, tehran university of medical sciences, tehran, iran and department of immunology, faculty of medicine, tehran university of medical sciences, tehran, iran ahmad reza jamshidi rheumatology research center, shariati hospital, tehran university of medical sciences, tehran, iran ali akbar amirzargar molecular immunology research center, tehran university of medical sciences, tehran, iran and department of immunology, faculty of medicine, tehran university of medical sciences, tehran, iran elham farhadi molecular immunology research center, tehran university of medical sciences, tehran, iran keramat nourijelyani department of epidemiology and biostatistics, school of public health, tehran university of medical sciences, tehran, iran sasan fallahi rheumatology research center, shariati hospital, tehran university of medical sciences, tehran, iran and department of rheumatology, shafa hospital, kerman university of medical sciences, kerman, iran

ankylosing spondylitis (as) is an inflammatory arthritis, which affects mainly spine and sacroiliac joints. according to recent studies, erap1 is the second most common candidate gene for  as susceptibility after hla-b27. the  aim of this study was to  determine the association of erap1 gene polymorphisms with as in iranian population. the study group comprised 387 iranian as patients and 316 h...

Journal: :iranian biomedical journal 0
khadijeh golabgir khademi ali mohammad foroughmand hamid galehdari saied yazdankhah mahdi pourmahdi borujeni zahra shahbazi

background: coronary artery disease (cad) is a multifactorial and heterogenic disease. recently, genome-wide association studies have reported that rs1333040 (c/t) and rs1004638 (a/t) single nucleotide polymorphisms (snps) in the 9p21 locus have very strong association with cad. this study aimed to examine these associations in southwest of iran. methods: blood samples were collected from 200 c...

Journal: :iranian journal of biotechnology 2008
mohammad ronaghi sadeq vallian masoud etemadifar

a single nucleotide polymorphism (snp) in cd24 has been associated with multiple sclerosis (ms) in a population based study. this snp results in the replacement of alanine (cd24a) by valine (cd24v) at amino acid 57 in the resulting polypeptide chain. in the current study, the genotyping of this snp and its contribution to ms in 217 patients and 200 healthy individuals of an iranian population w...

Journal: :gastroenterology and hepatology from bed to bench 0
khatoon karimi msc maral arkani akram safaei mohamad amin pourhoseingholi seyed reza mohebbi seyed reza fatemi

aim : leptin is a 16 kda polypeptide hormone which secreted by adipose tissue and has an important role in energy balance, insulin pathway and inflammation, because of that it may play an important role in colorectal cancer (crc). leptin exerts its effect through the leptin receptor (lepr) a member of the class i cytokine receptor family. background : we have investigated whether glutamine to a...

Journal: :iranian journal of pediatric hematology and oncology 0
mahbubeh nasiri department of biology, science and research branch, islamic azad university, fars, iran h galehdari department of genetics, university of shahid chamran, ahwaz, iran.سازمان اصلی تایید شده: دانشگاه آزاد اسلامی شیراز (islamic azad university of shiraz) m darbouy department of biology, science and research branch, islamic azad university, fars, iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) m yavarian hematology research centre,shiraz university of medical science, shiraz, iranسازمان اصلی تایید شده: دانشگاه آزاد اسلامی شیراز (islamic azad university of shiraz) b keikhaee thalassemia and hemoglobinopathies research center, ahwaz jondishapour university of medical sciences, ahwaz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)

abstract background von willebrand disease (vwd) is an autosomally inherited bleeding disorder with the prevalence of 1% based on population studies. the disease phenotype is due to quantitative and structural/functional defects in von willebrand factor (vwf) which is a glycoprotein with essential role as a carrier of fviii in circulation and also it serves the function as hemostasis regulator....

Journal: :RNA 2004
Yongfeng Jin Tengfei Bian

A comparison of Arabidopsis DNA sequences revealed that the final nucleotides at the 3' end of approximately half of the Arabidopsis mRNAs, immediately upstream of the poly(A) tail, differ from the corresponding genomic sequences. This suggests that extra nucleotides were added to these mRNAs at their 3' termini prior to polyadenylation. Among the mRNAs containing additional nucleotides, approx...

Journal: :biomacromolecular journal 0
neda assari department of cell and molecular biology, kharazmi university seiedabdolmajid angaji saeed morovvati department of molecular and biology, faculty of medical sciences, baghiyatallah university of medical sciences, tehran, iran

urokinase might play a role in the formation of kidney stones. this study was done to determine the association between +4065 t/c polymorphism at the 3′-untranslated region of urokinase gene and calcium kidney stones. this case-control study was carried out on 70 cases with a history of calcium kidney stones and 70 controls from the baqiyatallah hospital of tehran in 2013. the study of polymorp...

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