Michael Köttgen

Prof. Dr.
Michael Köttgen
Department of Medicine IVPhone: 0049-761-270-32990
michael.koettgen@uniklinik-freiburg.de
www.nephrolab.org/groups/michael-koettgen
CV
- 1997-1998 Residency, Department of Medicine, Medical Center – University of Freiburg
- 1998-2004 Postdoctoral Fellow, Institute of Physiology and Department of Medicine, University of Freiburg
- 2004-2009 Postdoc - Research Associate, Department of Biological Chemistry, Johns Hopkins University, Baltimore, USA
- 2010 Adjunct Professor, Department of Medicine, Johns Hopkins University, School of Medicine, Baltimore, USA
- Since 2010 Full Professor (W3), Department of Medicine IV, Medical Center – University of Freiburg
Focus of research
- Molecular pathogenesis of hereditary kidney disease
- Signal transduction
Selected publications
- Hofherr A, Köttgen M. Polycystic kidney disease: Cilia and mechanosensation revisited. Nat Rev Nephrol 12, 2016; 318-319.
- Hofherr A, Wagner CJ, Watnick T, Köttgen M. Targeted rescue of a polycystic kidney disease mutation by lysosomal inhibition. Kidney Int. 2016; 89,949-955.
- Hofherr A, Wagner C, Fedeles S, Somlo S, Köttgen M. N-glycosylation determines the abundance of the transient receptor potential channel TRPP2. J Biol Chem. 2014; 289, 14854-14867.
- Wegierski T, Steffl D, Kopp C, Tauber R, Buchholz B, Nitschke R, Kuehn EW, Walz G, Köttgen M. TRPP2 channels regulate apoptosis through the Ca2+ concentration in the endoplasmic reticulum. EMBO J. 2009; 28, 490-499.
- Woodward OM, Köttgen A, Coresh J, Boerwinkle E, Guggino WB, Köttgen M. Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout. Proc Natl Acad Sci USA. 2009; 106,10338-10342.
Research methods
- Drosophila genetics
- Live imaging - electrophysiology
- Genome editing