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Expression and CpG island methylation pattern of MMP-2 and MMP-9 genes in patients with congenital factor XIII deficiency and intracranial hemorrhage.

Ali Noroozi-AghidehZahra Kashani KhatibMajid NaderiAkbar DorgalalehMarjan YaghmaieMahdi ParyanShaban Alizadeh
Published in: Hematology (Amsterdam, Netherlands) (2020)
Our findings indicated that MMP-9 over-expression might be related to ICH in FXIII deficiency, and gene methylation effectively regulates its expression. Future researches will expand our understanding of the pathogenesis of ICH in congenital FXIII deficiency.
Keyphrases
  • poor prognosis
  • genome wide
  • dna methylation
  • binding protein
  • cell migration
  • replacement therapy
  • gene expression
  • copy number
  • genome wide identification
  • current status
  • optical coherence tomography