نتایج جستجو برای: g polymorphism in iranian shaul sheep population

تعداد نتایج: 17110160  

A SHrifiyan B Damavand H Naghoosi M.R Zali P Azimzadeh S Romani S.M.A Tahaei S.R Mohebi SH Baradaran-GHavami SH Derakhshani

Background & Aims: Hepatitis C virus (HCV) infection is a leading cause of chronic liver disease worldwide. The clearance of the HCV is dependent on cytokines control led by genetic. The purpose of this study was to investigate the impact of Lymphotoxin (LT-A) polymorphism at +252 in susceptibility to chronic hepatitis C. Methods: In this case-control study, 120 individuals infected by HCV and ...

Journal: :iranian journal of public health 0
n parvaneh dept. of pediatrics, infectious disease research center, children's medical center, tehran universit b pourakbari dept. of pediatrics, infectious disease research center, children's medical center, tehran universit kh daneshjoo dept. of pediatrics, imam khomeini hospital, tehran university of medical sciences, iran h ashraf dept. of pediatrics, infectious disease research center, children's medical center, tehran universit a salavati dept. of pediatrics, infectious disease research center, children's medical center, tehran universit s mamishi dept. of pediatrics, infectious disease research center, children’s medical center, tehran universit

background: cytokines and specially interferon-gamma (ifn-g) are largely responsible for the regulation of the protective im­mune response against mycobacterial infections. several studies have clarified the importance of common variants of ifn- g gene regarding the susceptibility to tuberculosis. bacille calmette-guérin (bcg) vaccine that is used to prevent se­vere forms of tuberculosis could ...

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...

2014
Zahra Akbari Mohammad Yaghoob Taleghani Hamid Asadzadeh Aghdaei Seyed Reza Mohebbi Mahdi Montazer Haghighi Mohsen Vahedi Hanieh Mirtalebi Pedram Azimzadeh Ehsan Nazemalhosseini-Mojarad Mohammad Reza Zali

Background and aim: Exonuclease1 (EXO1) is a member of the RAD2 nuclease family which is involved in mismatch repair (MMR) system and contributes to the maintenance of genomic stability, modulation of DNA recombination and cell cycle arrest mediation. K589E (rs1047840) as a potentially functional polymorphism in EXO1 gene may alter cancer risk by influencing its repair activity. Method: We desi...

Journal: : 2023

Abstract. As an excellent local sheep breed in China, Hu have the characteristics of producing more lambs and good motherhood. The purpose this study was to identify polymorphism mitogen-activated protein kinase 5 (MAP3K5) gene determine whether it associated with body size traits (body height, length, chest circumference, cannon circumference) sheep. MAP3K5 identified by using PCR amplificatio...

2017
Mahdi Montazer Haghighi Mohsen Vahedi Ehsan Nazemolhosseini Mojarad

Aim The aim of this study is to demonstrate the role of CCND1 gene polymorphism, A870G, in susceptibility to sporadic colorectal cancer in Iranian population. Background It has been distinguished that CCND1 gene is one of the main genes in Wnt signaling pathway which involves in generating colorectal cancer. Nonetheless, there is no consistent result in terms of association between the geneti...

Journal: :iranian journal of applied animal science 2015
f. ala noshahr a. rafat

the families of tgf-β proteins are the most important growth factors in the ovary for growth and differentiation of early ovarian follicles. three related oocyte-derived members of the transforming growth factor-β superfamily namely growth differentiation factor 9 (gdf9), bmp15 and bmpr-ib have been shown to be essential for follicular growth and ovulation. different mutations in the gdf9 gene ...

Introduction: Schizophrenia is a mental disorder affecting 1% of the world's population. Two of genes have been recognized to be involved in development of this disease: DRD2 and GSTM1. Methods: This case-control study included 100 patients suffering from schizophrenia who referred to Yazd Neuropsychiatry Hospital. Also, 100 healthy patients without schizophrenia were selected as the control g...

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