Catheline Vilain

Mechanisms of assembly and remodelling of the extracellular matrix

Biology and therapeutic targeting of vascular endothelial growth factor A

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

Chemical chaperone treatment reduces intracellular accumulation of mutant collagen IV and ameliorates the cellular phenotype of a COL4A2 mutation that causes haemorrhagic stroke