Skin and Bones: Studying the effects of MMP14 mutations

Ivo Johannes Hendrikus Marie de Vos

Research output: ThesisDoctoral ThesisInternal

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Abstract

Winchester syndrome (WS) is a rare genetic disease characterised by bone abnormalities, mitral valve insufficiency and acne. WS is caused by mutations in the MMP14 gene. This dissertation shows that a newly-discovered mutation in this gene causes mild WS. The underlying mechanism is the function of the MMP14 protein partly being limited by this mutation. In addition, the importance of MMP14 for tissue remodelling is shown. If abnormal, this causes bone abnormalities and acne. Finally, a new zebrafish model for WS is generated which can be used to develop new treatment options for this disease.
Original languageEnglish
Awarding Institution
  • Maastricht University
Supervisors/Advisors
  • van Steensel, M.A.M., Supervisor
  • Steijlen, Peter, Supervisor
  • Coull, B.J., Advisor, External person
Award date19 Dec 2018
Place of PublicationMaastricht
Publisher
Print ISBNs9789463800822
DOIs
Publication statusPublished - 2018

Keywords

  • MMP14
  • rare bone disease
  • acne

Cite this

de Vos, I. J. H. M. (2018). Skin and Bones: Studying the effects of MMP14 mutations. Datawyse / Universitaire Pers Maastricht. https://doi.org/10.26481/dis.20181219iv