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Association and gene-gene interaction analyses for polymorphic variants in CTLA-4 and FOXP3 genes: role in susceptibility to autoimmune thyroid disease.

Nusrath FathimaParimala NarneMohammed Ishaq
Published in: Endocrine (2019)
The genetic variation in CTLA-4 gene with reference to rs231775 polymorphism contributes to an increased predisposition to HT and GD. Also, in conjunction with FOXP3 gene variants it seems to influence the susceptibility to HT and GD respectively. The significance of these findings in combination with antithyroid antibody screening could plausibly contribute towards meticulous case-finding for effective treatment of HT and GD.
Keyphrases
  • copy number
  • genome wide
  • genome wide identification
  • regulatory t cells
  • genome wide analysis
  • multiple sclerosis
  • dna methylation
  • gene expression
  • dendritic cells
  • combination therapy