نتایج جستجو برای: iran polymorphism
تعداد نتایج: 208521 فیلتر نتایج به سال:
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...
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...
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...
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...
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 ...
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...
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...
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...
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...
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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