Mark Lommel

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Tobias Willer, Hane Lee, Mark Lommel et al. · Nature Genetics · 2012 · 237 citations · Full text

Somatic Variant, Mendelian Disorder, Genetic Disorder +6

Targeted disruption of the Walker–Warburg syndrome gene <i>Pomt1</i> in mouse results in embryonic lethality

Tobias Willer, Belén Prados, Juan Manuel Falcón‐Pérez et al. · Proceedings of the National Academy of Sciences · 2004 · 151 citations · Full text

Aberrant Processing of the WSC Family and Mid2p Cell Surface Sensors Results in Cell Death of <i>Saccharomyces cerevisiae</i> O-Mannosylation Mutants

Mark Lommel, Michel Bagnat, Sabine Strahl · Molecular and Cellular Biology · 2003 · 106 citations · Full text

Protein O-mannosylation is crucial for E-cadherin–mediated cell adhesion

Mark Lommel, Patrick R. Winterhalter, Tobias Willer et al. · Proceedings of the National Academy of Sciences · 2013 · 85 citations · Full text

Injury-induced MAPK activation triggers body axis formation in  <i>Hydra</i> by default Wnt signaling

Anja Tursch, Natascha Bartsch, Moritz Mercker et al. · Proceedings of the National Academy of Sciences · 2022 · 46 citations · Full text