Mohammad Reza Abbaszadegan
Department of Human Genetics, Immunology Research Centre, Avicenna Research Institute, Mashhad University of Medical Science, Mashhad, Iran|Medical Genetic Research Centre (MGRC), School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
[ 1 ] - Informative STR Markers for Marfan Syndrome in Birjand, Iran
Objective(s)Marfan syndrome (MFS) is a severe connective tissue disorder withan autosomal dominant inheritance pattern. Early diagnosis is critical in MFS. Because of the large size of fibrillin-1 gene (FBN1), the uniqueness of mutations, and the absence of genotype-to-phenotype correlations linkage analysis can be very helpful for early diagnosis of MFS. In this study, eight polymorphic marker...
[ 2 ] - تحلیل تصاویر ریزآرایه به منظور تشخیص نوع سرطان سینه
Background: Microarray technology is a powerful tool to study and analyze the behavior of thousands of genes simultaneously. Images of microarray have an important role in the detection and treatment of diseases. The aim of this study is to provide an automatic method for the extraction and analysis of microarray images to detect cancerous diseases. Methods: The proposed system consists of t...
[ 3 ] - تحلیل تصاویر ریزآرایه به منظور تشخیص نوع سرطان سینه
Background: Microarray technology is a powerful tool to study and analyze the behavior of thousands of genes simultaneously. Images of microarray have an important role in the detection and treatment of diseases. The aim of this study is to provide an automatic method for the extraction and analysis of microarray images to detect cancerous diseases. Methods: The proposed system consists of t...
[ 4 ] - Inherited Genetic Markers for Thrombophilia in Northeastern Iran (a Clinical-Based Report)
Background: Thrombophilia is a main predisposition to thrombosis due to a procoagulant state. Several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. These thrombophilic mutations are methylenetetrahydrofolate reductase (MTHFR, C677T, and A1298C), factor V Leiden (G1691A), prothrombin gene mutation (factor II, G20210A), and plasminogen...
[ 5 ] - Highly Efficient Transfection of Dendritic Cells Derived from Esophageal Squamous Cell Carcinoma Patient: Optimization with Green Fluorescent Protein and Validation with Tumor RNA as a Tool for Immuno-genetherapy
This study was conducted to optimize a highly efficient mRNA transfection into dendritic cells (DC) derived from esophageal squamous cell carcinoma (ESCC) patients. Applying an electroporation technique, in vitro synthesized Green Fluorescent Protein (GFP) mRNA was transfected as an indicator into the DCs derived from a healthy donor. Flow cytometry revealed 84.9% transfection efficiency for DC...
[ 6 ] - Chromosomal Analysis of Couples with Repeated Spontaneous Abortions in Northeastern Iran
Background Cytogenetic study of reproductive wastage is an important aspect in determining the genetic background of early embryogenesis. Approximately 15 to 20% of all pregnancies in humans are terminated as recurrent spontaneous abortions (RSAs). The aim of this study was to detect chromosome abnormalities in couples with RSAs and to compare our results with those reported previously. Materia...
Co-Authors