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Journal of Inherited Metabolic Disease|May 14, 2015
Golgi post-translational modifications and associated diseasesSven Potelle, André Klein, François Foulquier
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.
The Journal of Biological Chemistry|May 20, 2021
The promiscuous binding pocket of SLC35A1 ensures redundant transport of CDP-ribitol to the GolgiBenoît Ury, Sven Potelle, Francesco Caligiore, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 12, 2018
Involvement of thapsigargin- and cyclopiazonic acid-sensitive pumps in the rescue of TMEM165-associated glycosylation defects by Mn<sup>2</sup>Marine Houdou, Elodie Lebredonchel, Anne Garat, et al.
Biochimica Et Biophysica Acta. General Subjects|January 16, 2017
Evidence for splice transcript variants of TMEM165, a gene involved in CDGMarie-Ange Krzewinski-Recchi, Sven Potelle, Anne-Marie Mir, et al.
Biochimie|July 28, 2019
Dissection of TMEM165 function in Golgi glycosylation and its Mn<sup>2+</sup> sensitivityElodie Lebredonchel, Marine Houdou, Sven Potelle, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation DefectsWilly Morelle, Sven Potelle, Peter Witters, et al.
Human Molecular Genetics|March 25, 2016
Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasisSven Potelle, Willy Morelle, Eudoxie Dulary, et al.
Biochimica Et Biophysica Acta. General Subjects|November 8, 2017
Investigating the function of Gdt1p in yeast Golgi glycosylationEudoxie Dulary, Shin-Yi Yu, Marine Houdou, et al.
The Biochemical Journal|March 9, 2017
Manganese-induced turnover of TMEM165Sven Potelle, Eudoxie Dulary, Leslie Climer, et al.
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