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Mitochondrial dysfunction in NPC1-deficiency is not rescued by drugs targeting the glucosylceramidase GBA2 and the cholesterol-binding proteins TSPO and StARD1
Fluorescence polarisation activity-based protein profiling for the identification of deoxynojirimycin-type inhibitors selective for lysosomal retaining alpha- and beta-glucosidases
Corrigendum
Corrigendum: Xylose-configured cyclophellitols as selective inhibitors for glucocerebrosidase
In situ glucosylceramide synthesis and its pharmacological inhibition analysed in cells by 13C5-sphingosine precursor feeding and mass spectrometry
Consequences of excessive glucosylsphingosine in glucocerebrosidase-deficient zebrafish
Role of β-glucosidase 2 in aberrant glycosphingolipid metabolism: model of glucocerebrosidase deficiency in zebrafish
Dissociation of globotriaosylceramide and impaired endothelial function in α-galactosidase-A deficient EA.hy926 cells
Gluco-1H-imidazole: A New Class of Azole-Type beta-Glucosidase Inhibitor
1,6-Cyclophellitol Cyclosulfates: A New Class of Irreversible Glycosidase Inhibitor
Human Alpha Galactosidases Transiently Produced in Nicotiana benthamiana Leaves: New Insights in Substrate Specificities with Relevance for Fabry Disease
Carba-cyclophellitols Are Neutral Retaining-Glucosidase Inhibitors
Simultaneous quantitation of sphingoid bases by UPLC-ESI-MS/MS with identical C-13-encoded internal standards
Lysosomal glycosphingolipid catabolism by acid ceramidase: formation of glycosphingoid bases during deficiency of glycosidases
Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders.
Synthesis of a panel of carbon-13-labelled (glyco)sphingolipids