Novel Polycystin-2 regulation of ezrin in renal epithelia reveals insights into ADPKD cystogenesis
Good and bad consequences of proximal tubular dysfunction: lessons from human genetics
We investigate the pathogenesis of polycystic kidney disease (PKD) and other ciliopathies. Our focus lies in the study of pkd and cilia proteins in various systems to understand what changes in signal transduction explain the disease phenotypes.
Associations and Support:
- KFO 201
- Else-Kröner-Fresenius Stiftung
- European Renal Association (ERA)
- European Molecular Biology Organization (EMBO)