Panorama on congenital disorders of glycosylation (CDG): from 1980 to 2020 von Houdou, Marine, Foulquier, Francois

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Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects von Rujano, Maria A, Cannata Serio, Magda, Panasyuk, Ganna, Péanne, Romain, Reunert, Janine, Rymen, Daisy, Hauser, Virginie, Park, Julien H, Freisinger, Peter, Souche, Erika, Guida, Maria Clara, Maier, Esther M, Wada, Yoshinao, Jäger, Stefanie, Krogan, Nevan J, Kretz, Oliver, Nobre, Susana, Garcia, Paula, Quelhas, Dulce, Bird, Thomas D, Raskind, Wendy H, Schwake, Michael, Duvet, Sandrine, Foulquier, Francois, Matthijs, Gert, Marquardt, Thorsten, Simons, Matias

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Expanding the phenotype of metabolic cutis laxa with an additional disorder of N-linked protein glycosylation von Witters, Peter, Breckpot, Jeroen, Foulquier, François, Preston, Graem, Jaeken, Jaak, Morava, Eva

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Biometals and glycosylation in humans: Congenital disorders of glycosylation shed lights into the crucial role of Golgi manganese homeostasis von Foulquier, François, Legrand, Dominique

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Alkynyl monosaccharide analogues as a tool for evaluating Golgi glycosylation efficiency: application to Congenital Disorders of Glycosylation (CDG) von Vanbeselaere, Jorick, Vicogne, Dorothée, Matthijs, Gert, Biot, Christophe, Foulquier, François, Guerardel, Yann

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COG defects, birth and rise von Foulquier, François

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Cohen syndrome is associated with major glycosylation defects von Duplomb, Laurence, Duvet, Sandrine, Picot, Damien, Jego, Gaëtan, El Chehadeh-Djebbar, Salima, Marle, Nathalie, Gigot, Nadège, Aral, Bernard, Carmignac, Virginie, Thevenon, Julien, Lopez, Estelle, Rivière, Jean-Baptiste, Klein, André, Philippe, Christophe, Droin, Nathalie, Blair, Edward, Girodon, François, Donadieu, Jean, Bellanné-Chantelot, Christine, Delva, Laurent, Michalski, Jean-Claude, Solary, Eric, Faivre, Laurence, Foulquier, François, Thauvin-Robinet, Christel

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Reticular and Golgi glycosylation: Advances and associated diseases von Groux-Degroote, Sophie, Foulquier, Francois, Cavdarli, Sumeyye, Delannoy, Philippe

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Impaired glycosylation and cutis laxa caused by mutations in the vesicular H + -ATPase subunit ATP6V0A2 von Rajab, Anna, van Bokhoven, Hans, Foulquier, Francois, Gruenewald, Stephanie, Lefeber, Dirk, Van Maldergem, Lionel, Morava, Eva, Reynders, Ellen, Urban, Zsolt, Wevers, Ron, Mundlos, Stefan, Annaert, Wim, Nürnberg, Peter, Kornak, Uwe, Dimopoulou, Aikaterini, van Reeuwijk, Jeroen, Fischer, Bjoern, Budde, Birgit, Brunner, Han G, Matthijs, Gert

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Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG von Bammens, Riet, Mehta, Nickita, Race, Valérie, Foulquier, François, Jaeken, Jaak, Tiemeyer, Michael, Steet, Richard, Matthijs, Gert, Flanagan-Steet, Heather

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PUGNAc treatment leads to an unusual accumulation of free oligosaccharides in CHO cells von Mehdy, Ali, Morelle, Willy, Rosnoblet, Claire, Legrand, Dominique, Lefebvre, Tony, Duvet, Sandrine, Foulquier, François

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TMEM165 a new player in proteoglycan synthesis: loss of TMEM165 impairs elongation of chondroitin- and heparan-sulfate glycosaminoglycan chains of proteoglycans and triggers early... von Khan, Sajida, Sbeity, Malak, Foulquier, François, Barré, Lydia, Ouzzine, Mohamed

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Congenital disorders of glycosylation (CDG): Quo vadis? von Péanne, Romain, de Lonlay, Pascale, Foulquier, François, Kornak, Uwe, Lefeber, Dirk J., Morava, Eva, Pérez, Belén, Seta, Nathalie, Thiel, Christian, Van Schaftingen, Emile, Matthijs, Gert, Jaeken, Jaak

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Metalloglycobiology: The power of metals in regulating glycosylation von Durin, Zoé, Houdou, Marine, Legrand, Dominique, Foulquier, François

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Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis von Potelle, Sven, Morelle, Willy, Dulary, Eudoxie, Duvet, Sandrine, Vicogne, Dorothée, Spriet, Corentin, Krzewinski-Recchi, Marie-Ange, Morsomme, Pierre, Jaeken, Jaak, Matthijs, Gert, De Bettignies, Geoffroy, Foulquier, François

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High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect von Medina-Cano, Daniel, Ucuncu, Ekin, Nguyen, Lam Son, Nicouleau, Michael, Lipecka, Joanna, Bizot, Jean-Charles, Thiel, Christian, Foulquier, François, Lefort, Nathalie, Faivre-Sarrailh, Catherine, Colleaux, Laurence, Guerrera, Ida Chiara, Cantagrel, Vincent

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Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects von Morelle, Willy, Potelle, Sven, Witters, Peter, Wong, Sunnie, Climer, Leslie, Lupashin, Vladimir, Matthijs, Gert, Gadomski, Therese, Jaeken, Jaak, Cassiman, David, Morava, Eva, Foulquier, François

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Newly characterized Golgi-localized family of proteins is involved in calcium and pH homeostasis in yeast and human cells von Demaegd, Didier, Foulquier, François, Colinet, Anne-Sophie, Gremillon, Louis, Legrand, Dominique, Mariot, Pascal, Peiter, Edgar, Van Schaftingen, Emile, Matthijs, Gert, Morsomme, Pierre

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SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation von Durin, Zoé, Dubail, Johanne, Layotte, Aurore, Legrand, Dominique, Cormier-Daire, Valérie, Foulquier, François

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Golgi post-translational modifications and associated diseases von Potelle, Sven, Klein, André, Foulquier, François

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