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 · 239 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

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 · 153 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 · 107 citations · Full text

Life Sciences, Cell Biology, Genetics +10

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 · 86 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Hydra Mesoglea Proteome Identifies Thrombospondin as a Conserved Component Active in Head Organizer Restriction

Mark Lommel, Jennifer Strompen, Andrew L. Hellewell et al. · Scientific Reports · 2018 · 50 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +13