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

In recent years protein O-mannosylation has become a focus of attention as a pathomechanism underlying severe congenital muscular dystrophies associated with neuronal migration defects. A key feature of these disorders is the lack of O-mannosyl glycans on α-dystroglycan, resulting in abnormal baseme...

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Autors principals: Lommel, Mark, Winterhalter, Patrick R., Willer, Tobias, Dahlhoff, Maik, Schneider, Marlon R., Bartels, Markus F., Renner-Müller, Ingrid, Ruppert, Thomas, Wolf, Eckhard, Strahl, Sabine
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2013
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3876218/
https://ncbi.nlm.nih.gov/pubmed/24297939
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1316753110
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