نتایج جستجو برای: polymorphism gene cat

تعداد نتایج: 1215418  

حق پرست, سمیه , فصیحی رامندی, مهدی,

Introduction: The G to A mutation in KCNJ11 the ATP-sensitive potassium channel subunit, results in glutamate (E) to lysine (K) substitution at codon 23, and the A allele is shown to have a relationship with type II diabetes in our previous study. Their role in coronary heart disease (CHD) is not exactly obvious. We hypothesized that the polymorphism would be associated with increased susceptib...

Background and Objectives: Adiponectin is an adipokine, which is abundantly expressed in adipose tissue and has a potent roles in insulin sensitivity. This study aimed to test the association of single nucleotide polymorphism of rs1501299 of the adiponectin gene with adiponectin levels and type 2 diabetes.   Methods: This case-control study was conducted on 80 diabetic patients with fasting bl...

2016
Gadier El-Kheshen Maryam Moeini Mostafa Saadat

BACKGROUND Reactive oxygen species can attack and damage almost every molecule found in living cells, including proteins, carbohydrates, lipids, and DNA. For this reason, their production is normally tightly controlled. Among the most important defenses against these radicals are the superoxide dismutase (SOD) enzymes and catalase (CAT). Increasing attention has been given to the role of reacti...

Journal: :iranian journal of applied animal science 2015
s. joezy-shekalgorabi h. moradi shahr-e-babak m. abbasi firoozjaei a. ghorbani

acetyl-coenzyme a carboxylase α (acc-alpha) is considered as the key regulatory enzyme in fatty acid biosynthesis. acc-alpha gene is located on caprine chromosome 11 and is polymorphic in many goat breeds. in the current study, we aimed to find possible single nucleotide polymorphisms (snps) in the exon 1 region of the acc-alpha gene in iranian mahabadi goat breed. genomic dna was extracted fro...

Journal: :acta medica iranica 0
seyed hamid jamaldini department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. mojgan babanejad department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. reza mozaffari department of genetics, cardiogenetic research center, tehran, iran-department of genetics, shahid rajaie cardiovascular medical & research center, tehran, iran. nooshin nikzat department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. khadijeh jalalvand department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. azadeh badiei department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran.

coronary artery disease (cad) is the leading cause of mortality in many parts of the world. genome-wide association studies (gwas) have identified several genetic variants associated with cad in low-density lipoprotein receptor (ldlr) locus. this study was evaluated the possible association of genetic markers at ldlr locus with cad irrespective to lipid profile and as well as the association of...

Journal: :hepatitis monthly 0
zahra heidari infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, iran bita moudi infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, iran. tel: +98-5433295794, fax: +98-5433295794 hamidreza mahmoudzadeh sagheb infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, iran mehrnoosh moudi department of biology, science and research branch, islamic azad university, tehran, iran

conclusions the results indicated that there was a positive association between susceptibility to chronic hbv infection and tnf-α polymorphism. in addition, hbv patients carrying -308 gg, -857 cc, and -863 aa genotypes with lower serum levels of tnf-α had an increased risk of infection. background the host genetic background regulates the natural history of chronic hepatitis b virus (hbv) infec...

Journal: :iranian journal of biotechnology 2015
abdolreza salehi khadijeh nasiri mahdi aminafshar rohoallah sobhani mohammad bagher sayaadnejad

background: the osteopontin (opn) is a highly phosphorylated glycoprotein in numbers of bovine tissues and milk. opn has been reported to be associated with milk production in cattle.objective: the genotype and allelic frequencies for opn and its association with milk production will be evaluated in iranian holstein bulls.  materials and methods: bulls dna (100) was isolated. oligo was used for...

Journal: :journal of research in medical sciences 0
zilin ou hongbing chen gang liu chuo li shaoying lin jianwen lin

background: numerous studies have evaluated the association between the angiotensinogen (agt) t174m polymorphism and ischemic stroke(is) risk. however, the specific association is still controversial. materials and methods: in order to explore this association more deeply, we performed a meta-analysis. all of the relevant studies were identified from pubmed, embase, and chinese national knowled...

Journal: :international journal of pediatrics 0
leila mehdizadeh fanid assistant professor of cognitive neuroscience. department of animal biology faculty of natural sciences. university of tabriz, 29 bahman bolvard, tabriz, iran, ir. mohammad ali hosseinpour feizi professor of radiobiology, department of animal biology faculty of natural sciences. university of tabriz, 29 bahman bolvard, tabriz, iran, ir. mina adampour zare physiologist, department of animal biology faculty of natural sciences, university of tabriz, 29 bahman bolvard, tabriz, iran, ir. hasan shahrokhi child and adolescent psychiatrist md, research centre of psychiatry and behavioral science, tabriz university of medical science, tabriz, iran, ir.

background autism spectrum disorder (asd) is a intricate childhood neuropsychiatric disorder that is described by deficits in communication of verbal and non-verbal, reciprocal social interactions, stereotypic behaviors, interests, and activities. the studies of post-mortem neuro-anatomical anomalies have indicated that migration alterations could occur early during development (first trimester...

Journal: :iranian journal of public health 0
liya liu 1. dept. of epidemiology and health statistics, school of public health, central south university , changsha, china . ; 2. dept. of medical laboratory, hunan university of medicine , huaihua, china. lizhang chen 1. dept. of epidemiology and health statistics, school of public health, central south university , changsha, china . zhanzhan li 1. dept. of epidemiology and health statistics, school of public health, central south university , changsha, china . liang li 3. medical department of the first affiliated hospital of xiangya, central south university , changsha, china. jian qu 4. the institute of clinical pharmacology, central south university , changsha, china. jing xue 1. dept. of epidemiology and health statistics, school of public health, central south university , changsha, china .

there are much heterogeneity in the genetic variation of type 2 diabetes (t2d). the purpose of this study was to investigate the association of seven novel genetic loci identified in a recent genome-wide association studies (gwas) with t2d in chinese dong populations.a case-controlled study was performed in individuals of chinese dong nationality. the genotypes of pard3b (rs849230), loc729993 (...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید