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Dr. M. Nikbakht Dastjerdi,
Volume 12, Issue 1 (Spring 2015)
Abstract

  Abstract

 Background and Objectives

 A common polymorphism at codon 72 in the p53 gene has been associated with the increased risk for lung, oral, prostate, breast and colorectal cancers. We studied this polymorphism in acute myeloid leukemia specimen from Alzahra Hospital in Isfahan city.

 

 Materials and Methods

 In the present case-control study, 59 whole blood specimen from normal people and 59 acutemyeloid leukemia specimen were analyzed. p53 codon 72 genotypes were identified using allele-specificPCR. Chi-square test was used for the comparison of the frequency distribution of three genotypes of codon 72 in cases and control specimen. 

  

 Results

 Resulting PCR products were either 177bp for proline allele or 141bp for arginine allele. The genotype distribution for p53 polymorphism showed 11.9%, 81.4%, and 6.8% for the Arg/Arg, Arg/Pro, and Pro/Pro genotypes in control samples and 33.9%, 61%, and 5.1% in acute myeloid leukemia specimen, respectively. The differences in the distribution of p53 codon 72 polymorphism between the cases and controls were statistically significant (p = 0.04).

 

 Conclusions

 Deferasirox is relatively more effective than deferoxamine in reducing iron content of the liver and heart. Moreover, deferasirox is more effective in reducing cardiac iron content relative to liver iron content.

  

  


Dr. V. Dastjerdi, Dr. Sh. Salimi, Dr. M. Jafarian, Dr. N. Akbari, Dr. F. Yavari, S.s. Hashemi,
Volume 15, Issue 1 (Spring 2018)
Abstract

Abstract
Background and Objectives
Having more than 50 antigens, the Rh system is one of the most polymorphic blood group systems where clinically it is the second important blood group system after ABO. E,C,D,e,c are the most frequent antigens of this system. Considering the few reports on the high frequency of these antigens in regular donors of  Isfahan Blood Center, the aim of the study was to determine their phenotype and frequency, identify people with rare antigens, and form the data bank.
 
Materials and Methods
The study was descriptive with 310 regular O type donors referring to Isfahan Blood Center in 2016 included by Nonprobability-Convenience sampling. A blood suspension of 3-5% in the normal saline 0.9% was prepared and exposed to Rh anti sera by direct agglutination. Then, the Rh phenotype was determined based on the most common genotype.
 
Results
Among all the observed reactions, the highest frequency was e (95.16%) and the frequency rates of other antigens were 87.1%, 71.29%, 74.19%, and 32.9% for D-, C-, c-, and E-, respectively. The most common phenotype was R1r (27.42%), while the lowest being r"r (0.32%), and R2RZ (0.32%).
 
Conclusions 
Generally, the research on phenotype determination & RBC antigen frequencies in regular blood donor population would lead to accessible compatible blood types for regular blood recipients in minimum time and to reduction in hemolytic- alloimmune reactions.
 
 


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