نتایج جستجو برای: iran polymorphism

تعداد نتایج: 208521  

Journal: :iranian journal of immunology 0
shirin farjadian department of immunology abbas ghaderi department of immunology

background: hla genes are highly polymorphic and certain alleles are frequent only in specific populations. therefore, hla is a unique tool for studying the genetic relationship between different populations. iranians are ethnically diverse people and one of the major ethnic groups in iran is lur population inhabiting along the central and southern parts of zagros chain mountain. objectives: ge...

Journal: :iranian journal of basic medical sciences 0
mohammad zare-bidaki immunology of infectious diseases research center, rafsanjan university of medical sciences, rafsanjan, iran masoud karimi-googheri department of immunology, faculty of medicine, kerman university of medical sciences, kerman, iran gholamhossein hassanshahi molecular medicine research center, rafsanjan university of medical sciences, rafsanjan, iran nahid zainodini immunology of infectious diseases research center, rafsanjan university of medical sciences, rafsanjan, iran mohammad kazemi arababadi immunology of infectious diseases research center, rafsanjan university of medical sciences, rafsanjan, iran

evidence showed that chemokines serve as pro-migratory factors for immune cells. ccl3, ccl4 and ccl5, as the main cc  chemokines subfamily members, activate immune cells through binding to cc chemokine receptor 5 or ccr5. macrophages, nk cells and t lymphocytes express ccr5 and thus, affected ccr5 expression or functions could be associated with altered immune responses. deletion of 32 base pai...

Journal: :iranian journal of immunology 0
shirin farjadian department of immunology and abbas ghaderi department of immunology and

background: anthropological studies based on highly polymorphic hla genes pro-vide useful information for bone marrow donor registry, forensic medicine, disease as-sociation studies, as well as designing peptide vaccines against tumors, and infectious or autoimmune diseases. objective: this study was designed to investigate the genetic relationship of iranian arabs and jews using hla-class ii g...

2015
Shirzad GHOLAMI Farhang BABAMAHMOODI Rohallah ABEDIAN Mehdi SHARIF Abbas SHAHBAZI Abdolsattar PAGHEH Mahdi FAKHAR

BACKGROUND Infection with Trichostrongylus spp. is common among human and herbivorous in most parts of Iran, especially in southern and northern areas. The aim of present study was to identify Trichostrongylus spp. among human population using excreted egg specimens, by the molecular method, in Mazandaran Province, northern Iran. METHODS Overall, 33 positive fecal specimens were randomly samp...

Journal: :Archives of Iranian medicine 2007
Hamid-Reza Kianifar Saeed Talebi Jalil Tavakkol-Afshari Mohammad Esmaili Behrouz Davachi Azam Brook

BACKGROUND Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder of the intestinal transport of glucose and galactose, leading to watery diarrhea, dehydration, failure to thrive, and early death. METHODS In this study, we analyzed D28G mutation in 16 family members of a patient with typical presentation of congenital glucose-galactose malabsorption with polymerase ...

2012
A Miahipour H Keshavarz A Heidari A Raeisi M Rezaeian S Rezaie

BACKGROUND The main goal of present study was to detect polymorphism in MSP-1 gene which is a major blood stage candidate for vaccine in Plasmodium vivax by Single Strand Conformational Polymorphism-Polymerase Chain Reaction (SSCP-PCR). METHODS During 2008 to 2010 fifty samples were collected from Iranian patients with P. vivax in Hormozgan Province, southern Iran. All of the samples were det...

2016
Abozar Soleimani Yousef Rahmani Negin Farshchian Ali Delpisheh Kivan Khassi Afshar Shahmohammadi Nasrin Amirifard

BACKGROUND Breast cancer is the most common cancer among women in Iran and the world. Multiple environmental factors and genetic variations such as genetic polymorphisms are of its main causes. p53 gene plays an important role in conserving and sustaining the genome as a tumor suppressing gene. Change and polymorphism at codon 72 of p53 gene are correlated with increased risk of lung, mouth, en...

Journal: :Cytokine 2014
H Bakhshi N Borhani M Mohebali A Khamesipour M R Abai H Hajjaran L Tajedin Y Rassi A A Akhavan F Mohtarami M A Oshaghi

Great gerbils (Rhombomys opimus) are the most common gerbils in center to northeast of Iran as well as central Asia and serve as reservoirs for the zoonotic agents, including Leishmania major, the principal etiologic agent of zoonotic cutaneous leishmaniasis (ZCL). The outcome of L. major infection in gerbils is not uniform. Among several immune-related factors including cytokine genes, the pol...

Journal: :Gene, cell and tissue 2022

Background: Due to the lack of research on pediatric urolithiasis (PU) in Iran, this case-control study aimed assess correlation vitamin D receptor (VDR) gene polymorphisms Iranian population living Kerman, Iran. Methods: This was conducted 90 outpatients with urinary calculi (49 female and 41 male subjects a mean age 4.55 ± 3.005 years) healthy children (39 51 5.6 3.67 without history as contr...

AliReza Javadzadeh, Esmaeil Babaei, Mohammad Hossein Jabbarpour Bonyadi, Mortaza Bonyadi, neda norouzi,

Background & Aims: To investigate the association of CFI p.Gly119Arg polymorphism with Age-related macular degeneration (AMD). Materials & Methods: In this case-control study, the association of p.Gly119Arg polymorphism in CFI gene was investigated in 65 patients suffering from AMD and150 healthy age, sex and ethnicity matched unrelated people as control group. Both of the case and cont...

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