Dermatology and Genetic Medicine: A multidisciplinary research initiative aimed at translating basic science discoveries in genetic skin disease into clinical application.
In plain English
AI plain-English summaryA University of Dundee team is sequencing the DNA of hundreds of patients with rare genetic skin disorders to find the exact mutations that cause them. This matters because genetic skin diseases are under-researched, and many patients lack a precise diagnosis or effective treatment. The team is also tackling common conditions like eczema by searching for new genetic variants that drive the disease, including in the notoriously difficult-to-sequence filaggrin gene. Beyond discovery, the researchers are building a drug discovery pipeline modelled on a biotech company: they plan to run 15 high-throughput screens to find small-molecule drugs that hit newly identified targets, with the goal of partnering at least two of those targets with a pharmaceutical company. If successful, this work could turn fundamental genetic insights into real therapies for patients who currently have none. It could also streamline the diagnosis of rare skin disorders through whole-exome sequencing, giving families a name for their child’s condition. The project is a deliberate bridge between fundamental science and clinical application—it is not pure curiosity-driven research, but it is not yet at the bedside either.
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