نتایج جستجو برای: cytokine gene polymorphism

تعداد نتایج: 1261280  

Journal: :modares journal of medical sciences: pathobiology 2008
bahareh abd nikfarjam zahra amirghofran eskandar kamali

objective: in peripheral blood polymorphonuclear and mononuclear cells nitric oxide (no) could be synthesized by an enzyme called inducible no synthase (inos). inos gene (nos2a) is located on chromosome 17 at position 17q11.2-q12. no is released during inflammatory responses. in the present studies the frequency of nos2a gene polymorphisms and their effects on no production were investigated in...

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 ...

2015
Dnyanesh Amle Rashid Mir Alka Khaneja Sarita Agarwal Ravinder Ahlawat Prakash C Ray Alpana Saxena

BACKGROUND Vascular endothelial growth factor (VEGF) is a potent multifunctional cytokine which plays a key role in the pathogenesis of diabetic micro-vascular complications. Human VEGF gene is said to be highly polymorphic. Insertion/deletion (I/D) polymorphism of the 18 bp fragment at -2549 position of the promoter region in VEGF gene is said to be of particular interest. The study was aimed ...

Journal: :Problemi endokrinnoï patologìï 2023

Non-alcoholic fatty liver disease (NAFLD), the most common form of disease, is now recognized as a major public health problem worldwide. Tumor necrosis factor alfa (TNF-α), member TNF/TNFR cytokine family, an intercellular transmission molecule that has been reported in wide range human noninfection diseases. The aim study was to determine circulating levels TNF-α and nature its relationships ...

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 (...

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