مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

372
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Investigation of genetic variation of IL-4 receptor rs1801275 in patients with multiple sclerosis in Isfahan

Pages

  93-102

Abstract

 Aim and Background: Multiple Sclerosis (MS) is an autoimmune inflammatory disease that attacks myelinated axons in the central nervous system (CNS) resulting in destroying the myelin and the axon. According to high prevalence of disease in Iran, it needs to study different aspects of disease including factors influencing the pathogenesis and the other risk factors. Various type of Genetic Variants including polymorphisms may could highlight the relation between genetic and disease. In this study, we explored the relationship between IL-4 receptor polymorphism rs1801275 and disease risk. Material and Methods: In this study, IL-4receptor gene polymorphism was analyzed in a case-control study. All patients were selected as relapsing remitting (RR, n=100) and the control group consisted of 100 healthy (c, n= 100). High resolution melting analysis (HRMA) based on real-time PCR was performed to identify gene variation involved in disease. The results were analyzed by SPSS 20 software and also Hardy Weinberg equilibrium was tested for SNP. Also degree of heterozygosity and population analysis PIC was performed. Results: The results showed samples from control group consisted of 45% wild genotype (AA), 40% heterozygote (AG) and 15% homozygote (GG) for polymorphism rs1801275 while there was in patient group 20% wild genotype (AA), 58% heterozygote (AG) and 22% homozygote (GG). Conclusion: These results suggest that there was significant difference in allele count between control and patient groups. The allele frequency of IL-4 receptor polymorphism rs1801275was found significantly higher in patients (P-Value = 0. 022). IL4R polymorphisms may have a disease-promoting role in this population.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    AZADI, MARYAM, ALSAHEBFOSOUL, FERESHTEH, SALEHI, RASOUL, TAJBAKHSH, ELAHEH, & ETEMADIFAR, MASOUD. (2019). Investigation of genetic variation of IL-4 receptor rs1801275 in patients with multiple sclerosis in Isfahan. NEW CELLULAR & MOLECULAR BIOTECHNOLOGY JOURNAL, 9(34 ), 93-102. SID. https://sid.ir/paper/204717/en

    Vancouver: Copy

    AZADI MARYAM, ALSAHEBFOSOUL FERESHTEH, SALEHI RASOUL, TAJBAKHSH ELAHEH, ETEMADIFAR MASOUD. Investigation of genetic variation of IL-4 receptor rs1801275 in patients with multiple sclerosis in Isfahan. NEW CELLULAR & MOLECULAR BIOTECHNOLOGY JOURNAL[Internet]. 2019;9(34 ):93-102. Available from: https://sid.ir/paper/204717/en

    IEEE: Copy

    MARYAM AZADI, FERESHTEH ALSAHEBFOSOUL, RASOUL SALEHI, ELAHEH TAJBAKHSH, and MASOUD ETEMADIFAR, “Investigation of genetic variation of IL-4 receptor rs1801275 in patients with multiple sclerosis in Isfahan,” NEW CELLULAR & MOLECULAR BIOTECHNOLOGY JOURNAL, vol. 9, no. 34 , pp. 93–102, 2019, [Online]. Available: https://sid.ir/paper/204717/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button