نتایج جستجو برای: informative markers

تعداد نتایج: 246328  

Journal: :iranian journal of biotechnology 2008
ali fathi behzad ghareyazi ali haghnazari mohammad reza ghaffari seyed mostafa pirseyedi

the genetic diversity among 56 almond (prunus dulcis) genotypes was analysed using 35 microsatellite markers and 14 morphological traits. analysis of morphological traits revealed a wide range of variation among the studied genotypes. out of 35 simple sequence repeats (ssrs) markers, 25 were polymorphic, producing 215 alleles that varied from 2 to 16 with an average of 8.76 alleles per locus. r...

Assessment of genetic diversity is important step for exploitation from plant material in breeding programs. In this study, genetic diversity of 55 barley lines evaluated using SSR markers and also microsatellite markers were used to identify informative markers associated with phonological and yield traits related to drought escape including days to heading, grain filling period, days to physi...

Journal: :iranian journal of basic medical sciences 0
ezzat dadkhah department of human genetics, immunology research centre, avicenna research institute, mashhad university of medical science, mashhad, iran masood ziaee birjand hepatitis research centre, birjand university of medical sciences, birjand, iran mohammad hossein davari ophthalmology department, vali-e-asr hospital, birjand university of medical sciences, iran toba kazemi birjand atherosclerosis and coronary artery research centre, birjand university of medical sciences, birjand, iran mohammad reza abbaszadegan department of human genetics, immunology research centre, avicenna research institute, mashhad university of medical science, mashhad, iran medical genetic research centre (mgrc), school of medicine, mashhad university of medical sciences, mashhad, iran

objective(s)marfan syndrome (mfs) is a severe connective tissue disorder withan autosomal dominant inheritance pattern. early diagnosis is critical in mfs. because of the large size of fibrillin-1 gene (fbn1), the uniqueness of mutations, and the absence of genotype-to-phenotype correlations linkage analysis can be very helpful for early diagnosis of mfs. in this study, eight polymorphic marker...

Ezzat Dadkhah, Masood Ziaee Mohammad Hossein Davari Mohammad Reza Abbaszadegan, Toba Kazemi,

Objective(s)Marfan syndrome (MFS) is a severe connective tissue disorder withan autosomal dominant inheritance pattern. Early diagnosis is critical in MFS. Because of the large size of fibrillin-1 gene (FBN1), the uniqueness of mutations, and the absence of genotype-to-phenotype correlations linkage analysis can be very helpful for early diagnosis of MFS. In this study, eight polymorphic marker...

Journal: :medical journal of islamic republic of iran 0
ramin radpour department of clinical genetics and infertility, reproductive biomedicine research center of royaninstitute, tehran.iran. mahdi m. haghighi the genetic research center of social welfare and rehabilitation sciences university, tehran mina ohadi the genetic research center of social welfare and rehabilitation sciences university, tehran behrooz broumand rasoul akram hospital, iran university of medical sciences, tehran, iran. hossein najmabadi the genetic research center of social welfare and rehabilitation sciences university, tehran asghar hagibeigi the genetic research center of social welfare and rehabilitation sciences university, tehran

abstract background: autosomal dominant polycystic kidney disease (adpkd) is an inherited disorder with genetic heterogeneity. up to three loci are involved in this disease, pkdi on chromosome 16p13.3, pkd2 on 4q21, and a third locus of unknown location. methods: here we report the first molecular genetic study of adpkd and the existence oflocus heterogeneity for adpkd in the iranian population...

ASGHAR HAGIBEIGI, BEHROOZ BROUMAND, HOSSEIN NAJMABADI, MAHDI M. HAGHIGHI, MINA OHADI, RAMIN RADPOUR,

 ABSTRACT Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder with genetic heterogeneity. Up to three loci are involved in this disease, PKDI on chromosome 16p13.3, PKD2 on 4q21, and a third locus of unknown location. Methods: Here we report the first molecular genetic study of ADPKD and the existence oflocus heterogeneity for ADPKD in the Iranian populatio...

Journal: :Forensic Science International: Genetics Supplement Series 2017

In this study, the associations between ISSR markers with some agronomic traits in 22 ispaghula ecotypes were used by stepwise regression analysis. The results of stepwise regression analysis showed a significant association between traits and some of loci markers positions. For some traits was detected more than one informative marker. Totally 90 informative ISSR markers were revealed that due...

In this study, variation of beta-glucan content was assessed in 20 barley line and cultivars based on complete block design with three replications. Genetic diversity of these genotypes was also evaluated using ISSR markers. Beta-glucan extracted by an enzymatic method. Significant differences were found at the level of 1% among barley genotypes for beta-glucan content. The beta glucan content ...

Finding association between molecular markers and agronomic traits provides an excellent tool for indirect selection of a trait of interest in the population. In this study, stepwise regression analysis was used to estimate associations between ISSR and RAPD markers with some agronomic traits in 12 lemon balm ecotypes. Markers or bands were considered as independent variables and traits were co...

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