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Medecine Sciences : M/S|August 22, 2020
[Panorama on congenital disorders of glycosylation (CDG): from 1980 to 2020]Marine Houdou, François FoulquierBiochimica Et Biophysica Acta. General Subjects|June 30, 2020
Biometals and glycosylation in humans: Congenital disorders of glycosylation shed lights into the crucial role of Golgi manganese homeostasisFrançois Foulquier, Dominique LegrandJournal of Inherited Metabolic Disease|May 14, 2015
Golgi post-translational modifications and associated diseasesSven Potelle, André Klein, François FoulquierGlycoconjugate Journal|May 16, 2012
Glycosylation disorders of membrane traffickingClaire Rosnoblet, Romain Peanne, Dominique Legrand, et al.Glycobiology|November 30, 2010
How Golgi glycosylation meets and needs trafficking: the case of the COG complexEllen Reynders, François Foulquier, Wim Annaert, et al.Tissue & Cell|July 13, 2016
TMEM165 deficiencies in Congenital Disorders of Glycosylation type II (CDG-II): Clues and evidences for roles of the protein in Golgi functions and ion homeostasisEudoxie Dulary, Sven Potelle, Dominique Legrand, et al.Biochemical and Biophysical Research Communications|October 20, 2009
Screening for OST deficiencies in unsolved CDG-I patientsWendy Vleugels, Els Schollen, François Foulquier, et al.Biochimica Et Biophysica Acta. General Subjects|June 22, 2023
Metalloglycobiology: The power of metals in regulating glycosylationZoé Durin, Marine Houdou, Dominique Legrand, et al.Molecular Genetics and Metabolism|October 2, 2007
Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of GlycosylationRenate Zeevaert, François Foulquier, Jaak Jaeken, et al.Pageof 9