TNFSF15 (rs3810936) in Behçet’s disease

Faculty Medicine Year: 2020
Type of Publication: ZU Hosted Pages:
Authors:
Amany Mohamed Mohyldeen
Journal: The Egyptian Rheumatologist Taylor&Francis Group Volume:
Keywords : TNFSF15 (rs3810936) , Behçet’s disease    
Abstract:
The commonest genotype of rs3810936 in Egyptian BD patients was C/T. The TT genotype and the T allele frequencies were lower in BD patients than controls. T allele influences the expression of TNFSF15. The rs3810936 is associated with anterior uveitis and arthritis. These findings suggest a possible role for TNFSF15 in the pathophysiology of BD.
    
     
 
       

Author Related Publications

  • Amany Mohamed Mohyldeen, "Neutrophil/lymphocyte ratio and platelet/lymphocyte ratio in Behçet’s disease: which and when to use?", International League of Associations for Rheumatology, 2018 More
  • Amany Mohamed Mohyldeen, "Vitamin D Status in Hemophilia Patients Attending at Zagazig Universty Children Hospitals", Faculty of Medicine-Zagazig Universi, 2020 More
  • Amany Mohamed Mohyldeen, "Designing an autoverification system in Zagazig University Hospitals Laboratories: Preliminary evaluation on thyroid function profile", King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., 2014 More
  • Amany Mohamed Mohyldeen, "Role of Vitamin D Deficiency in Coronary Artery Disease and Cardiac Dysfunction", SCIENCEDOMAIN, 2016 More
  • Amany Mohamed Mohyldeen, "Serum miR-210 and miR-155 expression levels as novel biomarkers for rheumatoid arthritis diagnosis", Taylor&Francis Group, 2017 More

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