Felicitas Bosen

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome

Martin Schütz, Tanja Auth, Anna Gehrt et al. · Human Molecular Genetics · 2010 · 58 citations · Full text

Medicine, Genetics, Molecular Genetics +17

The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice

Indra Lübkemeier, René Andrié, Lars Lickfett et al. · Journal of Molecular and Cellular Cardiology · 2013 · 55 citations

Medicine, Cardiology, Genetics +12

The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice

Felicitas Bosen, Melanie Schütz, Anna Beinhauer et al. · FEBS Letters · 2014 · 32 citations

Life Sciences, Genetics, Molecular Genetics +17

Altered epidermal lipid processing and calcium distribution in the KID syndrome mouse model Cx26S17F

Felicitas Bosen, Anna Celli, Debra Crumrine et al. · FEBS Letters · 2015 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Human Connexin43E42K Mutation From a Sudden Infant Death Victim Leads to Impaired Ventricular Activation and Neonatal Death in Mice

Indra Lübkemeier, Felicitas Bosen, Jung‐Sun Kim et al. · Circulation Cardiovascular Genetics · 2014 · 13 citations · Full text

Medicine, Cardiology, Molecular Genetics +17