RESEARCH PAPER / 2026-03-23
Gorab deficiency in skin dermis accelerates aging and is associated with dysregulation of RCHY1-mediated P53 ubiquitination.
Abstract
Mutations in and functional inactivation of the Gorab gene cause gerodermia osteodysplastica (GO), a disease featuring wrinkled skin and osteoporosis, but the underlying mechanisms of skin aging remain incompletely understood.
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Research summary
Gorab deficiency in skin dermis accelerates aging through dysregulation of RCHY1-mediated P53 ubiquitination. The study addresses a genetic factor that may contribute to the mechanisms of skin aging, which is relevant to understanding the biological processes underlying aging and potential interventions.
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