نتایج جستجو برای: wga71 4 alleles and wga1 7 alleles

تعداد نتایج: 17091788  

Journal: :iranian journal of public health 0
mohammadhosain afrand medical scientific association, ali-ebne abitaleb faculty of medicine, islamic azad university, yazd branch, yazd, iran. nasrollah bashardoost dept. of biostatistics and epidemiology, ali-ebne abitaleb faculty of medicine, islamic azad university, yazd branch, yazd, iran. mohammad hasan sheikhha dept. of medical genetics, yazd diabetes research center, shahid sadoughi university of medical sciences, yazd, iran. mohammad afkhami-ardekani dept. of endocrinology, yazd diabetes research center, shahid sadoughi university of medical sciences, yazd, iran.

the aim of this study was to assess the possible association between genetic polymorphisms of the glutathione s-transferase (gst) gene family and the risk of the development of metabolic syndrome (ms) in zoroastrian females in yazd, iran.in this case-control study, gstm1, t1, and p1 polymorphisms were genotyped in 51 randomly selected ms patients and 50 randomly selected healthy controls on feb...

Journal: :تحقیقات دامپزشکی 0
عاطفه اسماعیل نژاد گروه پاتوبیولوژی، دانشکده دامپزشکی دانشگاه شیراز، شیراز–ایران غلامرضا نیکبخت گروه میکروبیولوژی و ایمونولوژی، دانشکده دامپزشکی دانشگاه تهران، تهران–ایران ندا خازنی اسکویی گروه میکروبیولوژی و ایمونولوژی، دانشکده دامپزشکی دانشگاه تهران، تهران–ایران فرهاد امینی گروه بهداشت و تعذیه دام و طیور، دانشکده دامپزشکی دانشگاه تهران، تهران–ایران

background: major histocompatibility complex (mhc) in chicken has profound influence on resistance/susceptibility to disease, and production and reproduction traits. microsatellite marker lei0258 is a genetic indicator for mhc haplotypes. recognizing diversity of mhc haplotypes in selectively bred populations will be helpful for selecting population resistant to disease and development of effec...

Journal: :international journal of molecular and cellular medicine 0
vahid kholghi oskooei cellular and molecular biology research center (cmbrc), babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) mohammad reza esmaeili dooki non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) haleh akhavan-niaki cellular and molecular biology research center (cmbrc), babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences)

cystic fibrosis (cf) is a life-limiting autosomal recessive disorder affecting principally respiratory and digestive system . it is caused by cystic fibrosis transmembrane conductance regulator (cftr) gene mutation. the aim of this study was to determine the extent of repeat numbers and the degree of heterozygosity for c.3499+200ta(7_56) and d7s523 located in intron 17b and 1 cm proximal to the...

Journal: : 2021

The allelofund of Ayrshire cattle the Komi Republic (n=340) and Kirov region (n=32) was evaluated using microsatellite DNA markers. It found that in studied populations, TGLA227 locus most polymorphic – 9 alleles, BM1824 TGLA126 loci had least alleles (3-4). allele 214 INRA23 (q=0.7387) with highest frequency Republic, 115 (q=0.7083) among animals region. average number per samples slightly hig...

فاضلی‌نسب, بهمن, نقوی, محمدرضا,

The knowledge of genetic diversity is a must to reduce genetic vulnerability during plant breeding efforts. In the present study 34 pairs microsatellite markers were used for germplasm analysis, estimation of the genetic relationship with the method of Nei and Lee and diversity and studying the capabiltiy of microsatellite marker between 4 resistant and sensitive wheat genotypes. Cluster anal...

Ali Akbar Amirzargar, Amir Amanzadeh Fazel Shokri, Manijeh Yousefi Behzadi Mohammad Ali Shokrgozar Nahid Ahmadi Nilufar Mohseni Zohreh Arjang

Background: Different studies have demonstrated that a small proportion of healthy individuals receiving the hepatitis B (HB) vaccine do not produce protective levels of anti-HB antibody, a phenomenon which could be linked to certain human leukocyte an-tigen (HLA) class-II alleles or haplotypes. Objectives: The present study was under-taken to determine the frequency of HLA class-II alleles in ...

عمرانی, میر داود, باقری, مرتضی, عبدی راد, عیسی, نوروزی پاک زاد, هاله,

  I Abdi Rad, [1] PhD M Bagheri [2] , MSc MD Omrani [3] , PhD H Norouzi Pakzad [4] , MD     Received: 18 Nov, 2008 Accepted: 21 Oct, 2009  Abstract Backgrounds & Aims: Some of polymorphisms are located in the promoter regions or other regulatory sequences of cytokine genes and are associated with increased or decreased amount of cytokines production. The aim of this study was to determine the r...

Journal: :Journal of Forestry Research 2021

Abstract Robinia pseudoacacia is an important afforestation tree introduced to China in 1878. In the present study, we examined genetic diversity among 687 strains representing four improved varieties and two secondary provenances, comprising 641 clones 46 seedlings. Ninety-one simple sequence repeats (SSRs) were selected through segregation analysis polymorphism characterization, all sampled i...

صحافی, سید رسول , طالبی, مجید , فتوت, رضا, ملکی زنجانی, بهرام ,

     The genetic diversity of 19 bitter vetch landraces (Vicia ervilia L.) from four provinces (East Azerbaijan, West Azerbaijan, Ardabil and Zanjan) of Iran was evaluated using 18 pairs of SSR primers. The extracted genomic DNA was amplified with eight pair primers and PCR products were separated on DNA sequencing gels. In this research, eight pair of SSR primers detected a total of 27 alleles...

Journal: :Journal of medical genetics 1999
S Searle J M Blackwell

A polymorphism in the promoter of human NRAMP1 encodes a Z-DNA forming dinucleotide repeat with four alleles: (1) t(gt)5ac(gt)5ac(gt)11g; (2) t(gt)5ac(gt)5 ac(gt)10g; (3) t(gt)5ac(gt) ac(gt)9g; and (4) t(gt)5ac(gt)9g. Alleles 1 and 4 are rare (gene frequencies approximately 0.001); alleles 2 and 3 occur at gene frequencies approximately 0.20-0.25 and approximately 0.75-0.80, respectively. Here,...

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