Plant glycosides and glycosidases: a treasure-trove for therapeutics K Kytidou, M Artola, HS Overkleeft, JMFG Aerts Frontiers in plant science 11, 521948, 2020 | 91 | 2020 |
Simultaneous quantitation of sphingoid bases by UPLC-ESI-MS/MS with identical 13C-encoded internal standards M Mirzaian, P Wisse, MJ Ferraz, ARA Marques, P Gaspar, SV Oussoren, ... Clinica Chimica Acta 466, 178-184, 2017 | 50 | 2017 |
Activity-based probes for glycosidases: profiling and other applications CL Kuo, E van Meel, K Kytidou, WW Kallemeijn, M Witte, HS Overkleeft, ... Methods in enzymology 598, 217-235, 2018 | 34 | 2018 |
Nicotiana benthamiana α-galactosidase A1. 1 can functionally complement human α-galactosidase A deficiency associated with Fabry disease K Kytidou, J Beekwilder, M Artola, E van Meel, RHP Wilbers, ... Journal of Biological Chemistry 293 (26), 10042-10058, 2018 | 24 | 2018 |
α-d-Gal-cyclophellitol cyclosulfamidate is a Michaelis complex analog that stabilizes therapeutic lysosomal α-galactosidase A in Fabry disease M Artola, C Hedberg, RJ Rowland, L Raich, K Kytidou, L Wu, A Schaaf, ... Chemical Science 10 (40), 9233-9243, 2019 | 18 | 2019 |
Human Alpha Galactosidases Transiently Produced in Nicotiana benthamiana Leaves: New Insights in Substrate Specificities with Relevance for Fabry Disease K Kytidou, TJM Beenakker, LB Westerhof, CH Hokke, GF Moolenaar, ... Frontiers in plant science 8, 1026, 2017 | 18 | 2017 |
Lysosomal storage diseases. For better or worse: adapting to defective lysosomal glycosphingolipid breakdown JM Aerts, MJ Ferraz, M Mirzaian, P Gaspar, SV Oussoren, P Wisse, ... eLS, 1-13, 2017 | 6 | 2017 |
Transfer of goods from plants to humans: Fundamental and applied biochemical investigations on retaining glycosidases K Kytidou Leiden University, 2020 | | 2020 |
Propositions K Kytidou | | |
α-D-Gal-cyclophellitol cyclosulfamidate and Gal-DNJ stabilize therapeutic lysosomal α-galactosidase A and Nicotiana benthamiana, A1. K Kytidou, MJ Ferraz, HS Overkleeft, J MF, G Aerts, M Artola | | |
Nicotiana benthamiana α-galactosidase A1. 1 can functionally K Kytidou, J Beekwilder, M Artola, E van Meel, R HP, GFM Wilbers, ... | | |
Diagnosis with activity-based probes of inherited glycosidase deficiencies using urine samples K Kytidou, I Denysiuk, CL Kuo, M Artola, HS Overkleeft, JMFG Aerts | | |
Cross species investigations with activity-based probes. Future prospects K Kassiani, R Katzy, E van Meel, JMFG Aerts | | |