Lotte Bang Pedersen
Cell Biology and Physiology
2100 København Ø
We study the molecular mechanisms by which primary cilia assemble, disassemble, and function to coordinate diverse signaling pathways during development and tissue homeostasis. Furthermore, we study the molecular basis underlying diseases caused by defective cilia (ciliopathies). We primarily use mammalian cell cultures as model systems.
For more information, check out the Cilia Group homepage: https://www1.bio.ku.dk/english/research/cbp/cilia/