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BMC Medical Genetics|October 10, 2013
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotypeEline van Meel, Daniel J Wegner, Paul Cliften, et al.
Nature Communications|January 17, 2013
hVps41 and VAMP7 function in direct TGN to late endosome transport of lysosomal membrane proteinsMaaike S Pols, Eline van Meel, Viola Oorschot, et al.
Methods in Enzymology|January 8, 2018
Activity-Based Probes for Glycosidases: Profiling and Other ApplicationsChi-Lin Kuo, Eline van Meel, Kassiani Kytidou, et al.
Traffic (Copenhagen, Denmark)|March 22, 2019
Localization of active endogenous and exogenous β-glucocerebrosidase by correlative light-electron microscopy in human fibroblastsEline van Meel, Erik Bos, Martijn J C van der Lienden, et al.
Developmental Cell|November 8, 2011
Autophagy proteins regulate the secretory component of osteoclastic bone resorptionCarl J DeSelm, Brian C Miller, Wei Zou, et al.
ACS Central Science|July 11, 2017
Correction to "Detection of Active Mammalian GH31 α-Glucosidases in Health and Disease Using In-Class, Broad-Spectrum Activity-Based Probes"Jianbing Jiang, Chi-Lin Kuo, Liang Wu, et al.
ACS Central Science|June 10, 2016
Detection of Active Mammalian GH31 α-Glucosidases in Health and Disease Using In-Class, Broad-Spectrum Activity-Based ProbesJianbing Jiang, Chi-Lin Kuo, Liang Wu, et al.
The Journal of Biological Chemistry|April 21, 2018
Nicotiana benthamiana α-galactosidase A1.1 can functionally complement human α-galactosidase A deficiency associated with Fabry diseaseKassiani Kytidou, Jules Beekwilder, Marta Artola, et al.
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