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Researcher
Romain Péanne
- Disciplines:Diagnostics, Laboratory medicine, Medicinal products
Affiliations
- Laboratory for Molecular Diagnosis (Division)
Member
From16 Jan 2012 → 30 Sep 2018
Projects
1 - 1 of 1
- New insights into ER and Golgi N-linked glycosylation - Contribution of CDG patients.From1 Oct 2012 → 30 Sep 2018Funding: FWO fellowships
Publications
1 - 8 of 8
- Congenital disorders of glycosylation (CDG): Quo vadis?(2018)
Authors: Romain Péanne, Eva Morava, Gert Matthijs
Pages: 643 - 663 - Congenital disorders of glycosylation (CDG): Quo vadis?(2018)
Authors: Romain Péanne, François Foulquier, Eva Morava, Gert Matthijs
Pages: 643 - 663 - Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects(2017)
Authors: Romain Péanne, Erika Souche, François Foulquier, Gert Matthijs
Pages: 3707 - 3729 - What is new in CDG?(2017)
Authors: Romain Péanne
Pages: 569 - 586 - MAN1B1-CDG: how stressed-out can the Golgi be?(2014)
Authors: Romain Péanne, Daisy Rymen, Nathalie Jurisch-Yaksi, Francois Foulquier, Wim Annaert, Gert Matthijs
Pages: 1105 - 1105 - Assessing ER and Golgi N-Glycosylation Process Using Metabolic Labeling in Mammalian Cultured Cells(2013)
Authors: Romain Péanne, Gert Matthijs, François Foulquier
Pages: 157 - 76 - Glycosylation disorders of membrane trafficking(2013)
Authors: Romain Péanne, François Foulquier
Pages: 23 - 31 - Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype.
Authors: Eline Blommaert, Romain Péanne, Frederik Staels, Erika Souche, Rik Schrijvers, François Foulquier, Gert Matthijs
Pages: 9865 - 9870