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

Evaluation of the role of Myhre syndrome associated SMAD4 variants in neurodevelopment and fibrosis

Generation and analysis of zebrafish models for human pathology

Identifying antifibrotic targets in complementary disease models for Myhre syndrome, a Mendelian multisystemic and profibrotic disorder

Research equipment for behavior analysis in zebrafish disease models.

Study of monogenic cutis laxa syndromes: paradigms for elastic fiber homeostasis

Regulatory landscaping: towards improved genetic diagnosis and therapy for SATB2-associated syndrome

Steunfonds Marguerite-Marie Delacroix: Regulatory landscaping: towards improved genetic diagnosis and therapy for SATB2-associated syndrome (Lisa Hamerlinck)

Upgrade of confocal FLIM microscope with two-photon excitation and detection modules

Etiopathogenetic study of inherited disorders of the connective tissue presenting with arterial malformations

Research into the genes involved in arterial tortuosity, and aortic aneurysms

Study of the molecular background and pathophysiology of monogenic disorders with structural cardiovasuclar anomalies

Genetic predictors of joint shape and cartilage mechanics