Publications by authors named "Matthew Manh Nguyen"

Article Synopsis
  • Werner syndrome is linked to mutations in the WRN helicase, which plays a critical role in DNA functions and is associated with premature aging.
  • WRN deficiency leads to abnormal levels of constitutive heterochromatin in human fibroblasts, specifically disrupting SATII pericentromeric satellite repeats and affecting protein interactions that organize heterochromatin.
  • The study concludes that while WRN loss alters heterochromatin organization independent of senescence, it shares characteristics with changes seen during the aging process.
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