Understanding human linkeropathies: study of the phenotypic and molecular consequences of defective biosynthesis of the glycosaminoglycan tetrasaccharide linker region.

Exploring the role of the extracellular matrix in pain using Ehlers-Danlos Syndromes as a model

Investigating pain-related phenotypes in mouse models of Ehlers-Danlos Syndromes.

Understanding human linkeropathies: study of the phenotypic and molecular consequences of defective biosynthesis of the glycosaminoglycan tetrasaccharide linker region.

Unexplored clinical and molecular consequences of the Ehlers-Danlos syndromes

Doctoral project Delfien Syx

Doctoral project Yike Kang

An integrated translational platform to gain insights in and improve diagnosis and management of the Ehlers-Danlos Syndromes.

An integrated translational platform to improve the management and outcome of rare heritable connective tissue disease

Chronic pain in Ehlers-Danlos syndrome: clinical and molecular characterization in human patients and a murine model

From variome to phenome: study of genetic defects underlying the heritable connective tissue disorder Ehlers-Danlos syndrome, and their pathogenic consequences on extracellular matrix organisation and function

Identification of novel genes and pathogenic pathways for osteogenesis imperfecta and Ehlers-Danlos syndrome, paradigm collagen disorders

Identifying a pain signature in classical Ehlers-Danlos syndrome

Linking extracellular matrix defects and chronic pain: the Ehlers-Danlos syndrome as a disease model

Study of mediators and pathways contributing to chronic pain in Ehlers-Danlos syndrome 

Study of mediators and pathways contributing to chronic pain in Ehlers-Danlos syndrome

Transmission Electron Microscopy Expertise Centre

Zebrafish as a model to study pain in Ehlers-Danlos syndromes

Research equipment for behavior analysis in zebrafish disease models.

Study of biological mechanisms involved in heritable connective tissue disorders, using the Ehlers-Danlos Syndrome as a paradigm

Study of the molecular pathogenesis of the Ehlers-Danlos syndrome

Study of molecular pathogenesis of Ehlers-Danlos syndrome/