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2. Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis. Potelle S; Morelle W; Dulary E; Duvet S; Vicogne D; Spriet C; Krzewinski-Recchi MA; Morsomme P; Jaeken J; Matthijs G; De Bettignies G; Foulquier F Hum Mol Genet; 2016 Apr; 25(8):1489-500. PubMed ID: 27008884 [TBL] [Abstract][Full Text] [Related]
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4. Dissection of TMEM165 function in Golgi glycosylation and its Mn Lebredonchel E; Houdou M; Potelle S; de Bettignies G; Schulz C; Krzewinski Recchi MA; Lupashin V; Legrand D; Klein A; Foulquier F Biochimie; 2019 Oct; 165():123-130. PubMed ID: 31351090 [TBL] [Abstract][Full Text] [Related]
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8. Fetal bovine serum impacts the observed N-glycosylation defects in TMEM165 KO HEK cells. Vicogne D; Houdou M; Garat A; Climer L; Lupashin V; Morelle W; Foulquier F J Inherit Metab Dis; 2020 Mar; 43(2):357-366. PubMed ID: 31415112 [TBL] [Abstract][Full Text] [Related]
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20. TMEM165 deficiency causes a congenital disorder of glycosylation. Foulquier F; Amyere M; Jaeken J; Zeevaert R; Schollen E; Race V; Bammens R; Morelle W; Rosnoblet C; Legrand D; Demaegd D; Buist N; Cheillan D; Guffon N; Morsomme P; Annaert W; Freeze HH; Van Schaftingen E; Vikkula M; Matthijs G Am J Hum Genet; 2012 Jul; 91(1):15-26. PubMed ID: 22683087 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]