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Researcher
François Foulquier
- Disciplines:Diagnostics, Laboratory medicine, Medicinal products
Affiliations
- Laboratory for Molecular Diagnosis (Division)
Member
From1 Apr 2009 → 30 Sep 2009 - Department of Human Genetics (Department)
Member
From1 Sep 2003 → 30 Apr 2007
Publications
1 - 10 of 42
- Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype.(2019)
Authors: Eline Blommaert, Romain Péanne, Daisy Rymen, Frederik Staels, Erika Souche, Rik Schrijvers, François Foulquier, Gert Matthijs
Pages: 9865 - 9870 - Use of Endoglycosidase H as a diagnostic tool for MAN1B1-CDG patients(2018)
Authors: Gert Matthijs, Eva Morava, François Foulquier
Pages: 3133 - 3141 - Congenital disorders of glycosylation (CDG): Quo vadis?(2018)
Authors: Romain Péanne, François Foulquier, 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 - Expanding the phenotype of metabolic cutis laxa with an additional disorder of N-linked protein glycosylation(2018)
Authors: Peter Witters, Jeroen Breckpot, François Foulquier, Eva Morava
Pages: 618 - 621 - Hypothesis: lobe A (COG1-4)-CDG causes a more severe phenotype than lobe B (COG5-8)-CDG(2018)
Authors: François Foulquier
Pages: 137 - 142 - Investigating the function of Gdt1p in yeast Golgi glycosylation(2018)
Authors: Marine Houdou, Gert Matthijs, François Foulquier
Pages: 394 - 402 - 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 - Manganese-induced turnover of TMEM165(2017)
Authors: Marine Houdou, Gert Matthijs, François Foulquier
Pages: 1481 - 1493 - Galactose supplementation in TMEM165-CDG patients rescues the glycosylation defects(2017)
Authors: Peter Witters, Gert Matthijs, David Cassiman, Eva Morava, François Foulquier
Pages: 1375 - 1386