نتایج جستجو برای: nos2a gene polymorphism

تعداد نتایج: 1189755  

Azita Shafighian, Hadi Mirzapour, Zahra Shahidi,

  Purpose: Estrogen as a crucial hormone during pregnancy acts by two types of receptors.   Estrogen receptor alpha, expressed by estrogen receptor 1 (ESR1) gene, is more abundant and   exists in all human reproductive systems. Association of ESR1 gene polymorphism has been   shown in some reproductive fields such as spontaneous abortion, endometriosis-related infertility   and in vitro fertili...

Journal: :international journal of advanced biological and biomedical research 2013
maryam khatibi hedayatullah roshanfekr jamal fayazi khalil mirzade

lactoferrin is a glycoprotein with molecular weight 80 kda iron-binding bond, which is composed of 690 amino acids. in most mammalian body fluids such as sweat, semen, tears, and saliva and milk neutrophil granules there. bovine lactoferrin gene be associated with susceptibility/resistance to mastitis and even with some economically important production traits. this study was carried out to det...

Journal: :journal of research in medical sciences 0
marjan mansourian department of biostatistics, school of public health, isfahan university of medical sciences, isfahan, iran shaghayegh haghjooy javanmard department of physiology, physiology research center, isfahan university of medical sciences, isfahan, iran

normal 0 false false false en-us x-none ar-sa previous studies have inspected the associations between adiponectin (adipoq) 276g/t polymorphisms and atherosclerosis, but the results are inconclusive. the aim of this study was to explore the relationship between polymorphism +276 g > t (rs1501299) in adipoq and atherosclerosis. a widespread search was directed to identify all studies on the asso...

Journal: :iranian journal of neurology 0
faraidoon haghdoost medical student research center and physiology research center, isfahan university of ‎medical sciences, isfahan, iran mahsa gharzi medical student research center, isfahan university of medical sciences, isfahan, iran‎ farough faez pharmacy student research center, isfahan university of medical sciences, isfahan, iran elinaz hosseinzadeh medical student research center, isfahan university of medical sciences, isfahan, iran‎ mohamadhasan tajaddini physiology research center, isfahan university of medical sciences, isfahan, iran laleh rafiei physiology research center, isfahan university of medical sciences, isfahan, iran

background: migraine is a common neurovascular disorder with multifactorial and polygenic inheritance. the aim of this study was to investigate the association of a migraine without aura and ala379val polymorphism of lipoprotein-associated phospholipase a2 (lp-pla2) gene in the iranian population. methods: in this study, 103 migraine patients and 100 healthy controls were enrolled. dna samples ...

Journal: :international journal of pediatrics 0
leila mehdizadeh fanid cognitive neuroscience, phd. department of biology faculty of natural sciences. university of tabriz, 29 bahman bolvard, tabriz, iran, ir. mina adampourezare physiology, msc. department of biology faculty of natural sciences. university of tabriz, 29 bahman bolvard, tabriz, iran, ir. mohammad ali hosseinpourfeizi radiobiology, prof. department of biology faculty of natural sciences. university of tabriz, 29 bahman bolvard, tabriz, iran. seyedgholamreza noorazar child and adolescent psychiatrist md & psychiatry assistant professor of tabriz university of medical science, tabriz, iran.

backgroundattention deficit hyperactivity disorder (adhd), is a multifactorial disorder and converging evidence has implicated abnormalities of dopamine neurotransmission. the aim of this study was to examine the association of -141 polymorphisms in drd2 gene with adha among iranian-azeri population.materials and methods a case–control association study included 153 patients with attention defi...

Journal: :journal of paramedical sciences 0
leila zarmakhi department of genetics,islamic azad university,tehran medical branch,tehran ,iran mehrdad hashemi department of genetics,islamic azad university,tehran medical branch,tehran ,iran

nitric oxide is an important vasorelaxant factor that it inhibits platelet adhesion and proliferation of smooth muscle cells. no is synthesized from l-arginine by means of endothelial nitric oxide synthase (enos) which is an isoform of  nitric oxide synthase.in the present study, we examined  possible association between the 27 base pair (bp) repeat  polymorphism in intron 4 of the  enos3 gene ...

Journal: :archives of clinical infectious diseases 0
mohammad naderi infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, ir iran mohammad hashemi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-5433295740, fax: +98-5433425728 shadi amininia department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran maryam rezaei department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran mohsen taheri genetic of non-communicable diseases research center, school of medicine, zahedan university of medical sciences, zahedan, ir iran

conclusions in conclusion, chit1 24 bp duplication might not be a candidate gene for susceptibility to ptb. larger studies are necessary to confirm these findings in various populations. results homozygous wild type, heterozygous and homozygous mutant frequencies of chit1 24 bp duplication polymorphism were 43.9%, 43.9% and 12.2% in controls and 42.8%, 45.1% and 12.1% in ptb patients. we found ...

Ali AliEsmailizadeh Koshkoieh Azam Torabi Azim Mousavizadeh Heydar Ghiasi Mohammad Reza Nassiry Mohammadreza Mohammad Abadi,

The growth hormone gene could be an attractive candidate gene for milk production in goats. Single-strand conformation polymorphism was used to identify polymorphism at the goat growth hormone (gGH) gene. For this purpose, genotyping of 90 Talli goat breeds was performed. Nine conformational patterns were observed in exon 4 of the gGH gene, with frequencies of 27.7% for the homozygous pattern (...

Journal: :American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011
A Schosser D Gaysina S Cohen-Woods E Domenici J Perry F Tozzi A Korszun C Gunasinghe J Gray L Jones E B Binder F Holsboer N Craddock M J Owen I W Craig A E Farmer P Muglia P McGuffin

The High-Throughput Disease-specific target Identification Program (HiTDIP) aimed to study case-control association samples for 18 common diseases. Here we present the results of a follow-up case-control association study of HiTDIP in major depressive disorder (MDD). The HiTDIP in MDD was conducted in a sample of 974 cases of recurrent MDD of white German origin collected at the Max-Planck Inst...

B.R. Yadav D.S. Kale, 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...

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