M. Schnichels

The connexin31 F137L mutant mouse as a model for the human skin disease erythrokeratodermia variabilis (EKV).

K. Willecke, M. Kretz, E. Winterhager, 2007, Human molecular genetics.

Characterization of connexin31.1-deficient mice reveals impaired placental development.

K. Willecke, M. Kretz, S. Lye, 2007, Developmental biology.

Characterization of connexin30.3-deficient mice suggests a possible role of connexin30.3 in olfaction.

J. Degen, K. Willecke, E. Dere, 2007, European journal of cell biology.

Connexin 30.3 Is Expressed in the Kidney But Not Regulated by Dietary Salt or High Blood Pressure

K. Willecke, Q. Zheng-Fischhöfer, J. Peti-Peterdi, 2008, Cell communication & adhesion.

Connexin31.1 deficiency in the mouse impairs object memory and modulates open-field exploration, acetylcholine esterase levels in the striatum, and cAMP response element-binding protein levels in the striatum and piriform cortex

K. Willecke, E. Dere, J. Huston, 2008, Neuroscience.

Connexin 30.3 Is Expressed in the Kidney But Not Regulated by Dietary Salt or High Blood Pressure

K. Willecke, J. Peti-Peterdi, A. McDonough, 2008, Cell Communication & Adhesion.