نتایج جستجو برای: gene polymorphisms

تعداد نتایج: 1168765  

رحیمی میانجی, قدرت, فرهادی, ایوب, همتی دوست, وحید,

Mastitis is one of the most prevalent and costly diseases affecting dairy cattle production. In the present study, effects of tumor necrosis factor (alpha isomer) gene (TNF-α) polymorphisms on milk somatic cell count (SCS) and subclinical mastitis was investigated in 121 Holstein dairy cattle. The polymorphisms of a 303 bp fragment of TNF-α gene were investigated by PBR and PCR-SSCP techniques....

Journal: :Future Virology 2021

Aim: This study aimed to investigate the relationship between severe novel coronavirus pneumonia (NCP) and hypercoagulable conditions that predispose patients thrombosis such as prothrombin gene ( F2) rs1799963 (G20210A), factor V Leiden F5) rs6025 (G1691A) PAI-1 (rs1799768). Patients: NCP-diagnosed 62 previously healthy were enrolled for investigation of thrombophilia-related polymorphisms. Ma...

Journal: :genetics in the 3rd millennium 0
اشرف احمدی شادمهری ashraf ahmadi shadmehri science and research center, islamic azad university, tehran, iranدانشگاه آزاد اسلامی، واحدعلوم و تحقیقات، تهران، ایران علی اکبر امیرزرگر ali akbar amirzargar department of immunogenetic, science faculty, tehran university of medical science, tehran, iranبخش ایمونوژنتیک، دانشکده علوم، دانشگاه علوم پزشکی تهران، تهران، ایران ، محمد حسین نیکنام mohammad hossein niknam department of immunogenetic, science faculty, tehran university of medical science, tehran, iranبخش ایمونوژنتیک، دانشکده علوم، دانشگاه علوم پزشکی تهران، تهران، ایران اعظم احمدی شادمهری azam ahmadi shadmehri genetic counseling centre, welfare organization of southern khorasan, iranسازمان بهزیستی، مرکز مشاوره ژنتیک خراسان جنوبی، ایران

the immunoreceptor programmed cell death-1 (pd-1) is a cell surface molecule that is reported to play an important role in the regulation of peripheral tolerance. it has been shown that pd-1 gene is associated with susceptibility to the autoimmune disease systemic lupus erythematosus (sle) in humans. however, there are no reports on the association between this gene and multiple sclerosis (ms)....

Journal: :Annals of the Rheumatic Diseases 2001

Farzaneh Ghasemi, Mehri Khatami, Mohammad Mehdi Heidari, Reyhane Chamani,

Background: CDKN2A, encoding two important tumor suppressor proteins p16 and p14, is a tumor suppressor gene. Mutations in this gene and subsequently the defect in p16 and p14 proteins lead to the downregulation of RB1/p53 and cancer malignancy. To identify the structural and functional effects of mutations, various powerful bioinformatics tools are available. The aim of this study is the ident...

مروتی, سعید, ناصری ارزنق, فاطمه,

Background and Objectives: Recurrent Spontaneous Abortions (RSA) is defined as the repeated occurrence of 2 or more miscarriages before 20th week of gestation. RSA is a multifactorial disorder and genetic defects are considered as one of the major risk factors for recurrent miscarriage. It seems the progesterone receptor gene polymorphisms to be one of the genetic factors involved in the occurr...

درخشان, فرامرز, رومانی, سارا, زالی, محمدرضا, عظیم زاده, پدرام, محبی, سیدرضا, واحدی, محسن, فاطمی, سیدرضا ,

Background & Objective: Cytokines are immune system factors known to play a key role in both HCV clearance and the development of infection the impact of host genetic factors on the clinical outcome of HCV infection has not been elucidated. On the other hand, the impact of Genetic changes like Single nucleotide polymorphisms on expression rate and function of Cytokine is under study. The aim ...

Introduction: Long-term levodopa treatment of Parkinson’s disease (PD) is frequently complicated by spontaneously occurring involuntary muscle movements called dyskinesia. The exact pathological mechanism of this complication has not yet been elucidated. We have previously demonstrated that in PD patients the vulnerability to develop peripheral but not orofacial dyskinesia is associated w...

ژورنال: Medical Laboratory Journal 2014
Esmaeili, R, Hassanzadeh, T,

Abstract Background and Objective: Metabolic syndrome called a cluster of several metabolic disorders is associated with increased risk of cardiovascular diseases. Genetic differences in leptin receptor gene are related with the concentration and activity of leptin in that these discrepancies can influence lipid levels. We aimed to determine the association between the leptin receptor gene p...

ژورنال: کومش 2020

Introduction: PGC-1α gene plays an important role in regulating cellular energy metabolism and stimulating the increased cell mitochondrial mass. Understanding the status of this gene polymorphism in non-athletic male adolescents may be helpful in choosing and identifying the sport talented male adolescents. The purpose of the present study was to investigate possible association between PGC-1α...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید