نتایج جستجو برای: genotype frequency

تعداد نتایج: 565280  

2011
Martina Miluchová Michal Gábor Anna Trakovická

The goal of the paper was to identify  lactoglobulin gene polymorphism and analyse of genotype structure in population Slovak spotted breed. The  lactoglobulin (LGB) expressed in milk and is important in the evaluation of milk production potential and butterfat and protein content. LGB is localized on bovine chromosome 11. The AA genotype of LGB is associated with higher milk yield, the BB ge...

Journal: :iranian journal of applied animal science 2015
k.f. mahrous m.s. hassanane m. abdel mordy h.i. shafey h.e. rushdi

the genetic polymorphism of some genes related to meat production in three egyptian sheep breeds (barki, rahmani and osseimi) was studied. the candidate genes were: calpastatin, myostatin, diacylglycerol-acyltransferase1, insulin-like growth factor binding protein-3 and booroola fecundity gene. the technique applied was the restriction fragment length polymorphism for the polymerase chain react...

Azam Brook Houshang Rafatpanah Jalil Tavakkol Afshar Mehdi Seilanian Toosi Mohamad Reza Ghavam Nassiri Mona Malekzadeh Moghani,

Background and Objective: Host genetic factors such as cytokine gene polymorphisms as well as Helicobacter pylori (H. pylori) infection have been found to be associated with gastric cancer risk . Interleukin 1 is a pro-inflammatory cytokine involved in H. pylori-induced gastric inflammation. Therefore, w...

اسلامی, گیلدا, شمس, علی, قباد زاده, سمیرا, میرغنی زاده, سید علی,

Introduction: NKG2D receptor is one of the activator receptors of immune cells. In humans, NKG2D gene has two single nucleotide polymorphisms (SNP)(rs1049174G>C). According to other studies, GG SNP makes a high affinity receptor for NKG2D ligands whereas, CC polymorphism reduces NKG2D affinity for their ligands. The present study investigates NKG2D SNPs in patients with breast cancer in Yazd f...

Journal: :medical journal of islamic republic of iran 0
v hadavi from the department of human genetics & anthropology, school of public health & institute of public health research, tehran university of medical sciences, p.d.box 14155-6446, tehran dd farhud from the department of human genetics & anthropology, school of public health & institute of public health research, tehran university of medical sciences, p.d.box 14155-6446, tehran mh sanati the national research center for genetic engineering and biotechnology, tehran sm nabavi the shahed medical university, m seyedian tehran university of medical sciences, roozbeh hospital m hushmand the national research center for genetic engineering and biotechnology

multiple sclerosis (ms) is a chronic inflammatory disorder of the central nervous system, with a complex etiology that includes a strong genetic component. the chromosome 19q 13 region surrounding the apolipoprotein e (apoe) gene has shown consistent evidence of involvement in ms. in a cross-sectional study, to show the apoe genotype and allele frequency in the ms population of iran in comparis...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تحصیلات تکمیلی صنعتی کرمان - پژوهشکده برق و کامپیوتر 1390

a phase-locked loop (pll) based frequency synthesizer is an important circuit that is used in many applications, especially in communication systems such as ethernet receivers, disk drive read/write channels, digital mobile receivers, high-speed memory interfaces, system clock recovery and wireless communication system. other than requiring good signal purity such as low phase noise and low spu...

Journal: :iranian journal of public health 0
t golmohamadi a nikzamir m nakhjavani m zahrai a amirzargar r saffari

angiotensin i-converting enzyme (ace) gene polymorphism; genotype dd or d allele may be involved with an increased susceptibility to type 2 diabetes and diabetic nephropathy (dn). we examined the frequency of ace gene polymorphism in 170 patients (85 type 2 diabetes with nephropathy and 85 without it) in tehran, iran. dna was extracted from the white blood cells and the i/d polymorphism of the ...

Background & Aims: Behcet’s disease (BD) is an inflammatory vasculitis of unclear etiology. MCP-1 gene is a member of the C-C chemokines family that is a chemotactic factor for monocytes. The results obtained have shown that the -2518A/G polymorphism of MCP-1 gene is associated with BD. The aim of this study was to evaluate the possible involvement of this polymorphism and Behcet&rsq...

Journal: :iranian journal of veterinary research 2014
r. deb u. singh s. kumar r. singh g. sengar

the aim of the present study was to screen the genotype profile of bovine kappa-casein gene among frieswal (hf × sahiwal) crossbred cattle developed in india. a total number of two hundred frieswal cows were evaluated for hinfi rflp based genotyping of kappa-casein gene. we observed that only two genotypes (aa and ab) exist among the studied population with the genotype frequency of 0.58 (n=117...

Journal: :international journal of reproductive biomedicine 0
mehdi nikbakht dastjerdi roshanak aboutorabi bahram eslami farsani

background: endometriosis is a female health disorder that occurs when cells from the lining of the uterus grow in other areas of the body. the cause of endometriosis is unknown. objective: the purpose of this study was to investigate tp53 gene codon 72 polymorphism in women with endometriosis and compared it with healthy samples in isfahan. materials and methods: we undertook a case-control st...

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