نتایج جستجو برای: lipl41 gene

تعداد نتایج: 1141392  

Journal: :reports of biochemistry and molecular biology 0
mahnaz mahmoudi rad skin research center, shahid beheshti university of medical sciences, tehran, iran niki mahmoudi rad skin research center, shahid beheshti university of medical sciences, tehran, iran yasaman mirdamadi tel: +49- 176- 64713028; fax: +98 21- 22744393

background: the multifunctional transforming growth factor beta (tgf-β) is a glycoprotein that exists in three isoforms. tgf-β3 expression increases in fetal wound healing and reduces fibronectin and collagen i and iii deposition, and also improves the architecture of the neodermis which is a combination of blood vessels and connective tissue during wound healing. fibroblasts are key cells in t...

Journal: :iranian journal of applied animal science 2015
m. hosseinpour mashhadi m.r. nassiri m. mahmoudi m. rastin n.e.j. kashan

quantitative traits locus for milk production traits has been described on centromeric end of bovine chromosome 14. reports name the acyl coa: diacylglycerol acyltransferase (dgat1) gene as a potential candidate gene with dinucleotide substitution (aa to gc) in exon viii which causes the change of lysine to alanine in amino acid (k232a).the aim of the present study was to estimate the frequency...

Journal: :journal of livestock science and technologies 2013
y. mehdizadeh gazooei a. niazi m. j. zamiri

the fecb, a mutation in the bone morphogenetic protein receptor ib (bmpr-ib) gene, which increases the fecundity of booroola merino sheep, and fecgh, a mutation in the growth and differentiation factor 9 (gdf9), which affects the fecundity of cambridge and belclare sheep in a dose sensitive manner, were analyzed as candidate genes associated with the prolificacy in rayini goats. these polymorph...

Journal: :international journal of advanced biological and biomedical research 2014
fatemeh amraei hedayatollah roshanfekr jamal fayazi mohammad bojarpour

objective: identity the genetic aspects and major gene influence on energy balance, milk production, fertility, food safety and consumer are the recent interests of genetic and breeding researchers. methods: najdi cattle is the most prominent breeds in khuzestan province. to do this plan in shoushtar najdi cattle station, blood samples were taken from 15 najdi cattles. dna was extracted from wh...

Journal: :iranian red crescent medical journal 0
ziba soltani genomic research center, shahid beheshti university of medical sciences, tehran, ir iran fatemeh karami department of medical genetics, school of medicine, tehran university of medical sciences, tehran, ir iran vahidreza yassaee genomic research center, shahid beheshti university of medical sciences, tehran, ir iran feyzollah hashemi gorji genomic research center, shahid beheshti university of medical sciences, tehran, ir iran mahdieh talebzadeh genomic research center, shahid beheshti university of medical sciences, tehran, ir iran mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, ir iran; genomic research center, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122439959, fax: +98-2122439961

conclusions this finding may help improve early detection, differential diagnosis, genetic counseling, and even treatment of patients with pku. introduction phenylketonuria (pku) is an autosomal recessive inborn error of phenylalanine metabolism, which is caused by mutation in phenylalanine hydroxylase (pah) gene. most of the pah mutations are missense mutations (67%), which are followed by sma...

Journal: :iranian journal of diabetes and obesity 0
sayed alireza mirsane shima shafagh nasrin oraei

abstract tuberculosis and diabetes mellitus are the most important reasons in mortality all over the world. it’s clear that reviewing of relationship between tuberculosis (tb) and diabetes mellitus (dm) is necessary; on the other hand it’s found that fto gene has the positive relationship with metabolic issues. therefore, it’s necessary pay attention to the above and dangerous sicknesses, espec...

Journal: :iranian journal of public health 0
eskandar omidinia 1. genetic and metabolism research group, pasteur institute of iran , tehran, iran. fariba mashayekhi mazar 2. veterinary dept., islamic azad university, kahnooj branch , kerman, iran. parima shahamati 3. critical care nursing dept., zanjan school of nursing and midiwifery, zanjan university of medical sciences , zanjan, iran. anvarsadat kianmehr 4. dept. of medical biotechnology, school of advanced medical sciences, tabriz university of medical sciences , tabriz, iran. hamid shahbaz mohammadi 1. genetic and metabolism research group, pasteur institute of iran , tehran, iran.

the gene coding claudin (cldn5) is located on 22q11. since the proteins of cldn5 family are a ma-jor component for barrier-forming tight junctions, it may be important to test whether or not the cldn5 locus could be associated with schizophrenia.a total of 150 individuals affected with schizophrenia and 150 healthy persons were recruited. the relation-ship between the three single nucleotide po...

Journal: :medical journal of islamic republic of iran 0
a kazemi immunology and parasitology department , school of medicine, tabriz university of medical sciences, tabriz, i.r. iran g.d robson d.w denning

background and objectives: annexin is the common name for genes and proteins that were identified as calcium-dependent phospholipid-binding proteins. recently a more complex set of functions has been recognized for this superfamily of proteins including in vesicle trafficking, cell division, apoptosis, calcium signalling, mineralization, crystal nucleation inside the extracellular organelles-ma...

Journal: :iranian journal of psychiatry and behavioral sciences 0
reza bidaki mina zarei department of psychiatry rafsanjan university of medical sciences, rafsanjan, iran ali khorram toosi mitra hakim shooshtari

ône-third of population deal with sleep disorders which might be due to social, economic or medical problems. studies on twins have indicated the role of genetic factors in these disorders. monozygotic twins have a very similar hypnogram. â higher prevalence of some sleep disorders is reported in relatives of the patients with these disorders. genes also affect sleep disorders as well as some o...

Journal: :gastroenterology and hepatology from bed to bench 0
rouhallah najjar sadeghi pedram azimzadeh mohsen vahedi mahsa molaei seyed reza mohebbi homayon zojaji

aim : the purpose of this study was to assess the incidence of 16bp insertion of intron 3 p53 in gastritis lesion and its correlation with clinicopathological aspects. background : p53 alterations have been implicated in the development of gastric malignancies. patients and methods : 97 gastritis and normal adjacent tissues were investigated for p53 gene analysis using pcr-sequencing of intron3...

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