E. van Meel

发表

Imaging and imagination: understanding the endo-lysosomal system

J. Klumperman, E. van Meel, 2008, Histochemistry and Cell Biology.

Autophagy proteins regulate the secretory component of osteoclastic bone resorption.

H. Virgin, W. Zou, S. Teitelbaum, 2011, Developmental cell.

Vacuolization of mucolipidosis type II mouse exocrine gland cells represents accumulation of autolysosomes

J. Klumperman, E. van Meel, V. Oorschot, 2011, Molecular biology of the cell.

Disruption of the Man‐6‐P Targeting Pathway in Mice Impairs Osteoclast Secretory Lysosome Biogenesis

F. Ross, J. Klumperman, E. van Meel, 2011, Traffic.

Mislocalization of phosphotransferase as a cause of mucolipidosis III αβ

E. van Meel, S. Kornfeld, Y. Qian, 2014, Proceedings of the National Academy of Sciences.

Activity-Based Probes for Glycosidases: Profiling and Other Applications.

M. Artola, M. Witte, E. van Meel, 2018, Methods in enzymology.

Localization of active endogenous and exogenous β‐glucocerebrosidase by correlative light‐electron microscopy in human fibroblasts

H. Overkleeft, A. Koster, E. Bos, 2019, Traffic.

Analysis of Mucolipidosis II/III GNPTAB Missense Mutations Identifies Domains of UDP-GlcNAc:lysosomal Enzyme GlcNAc-1-phosphotransferase Involved in Catalytic Function and Lysosomal Enzyme Recognition*

E. van Meel, S. Kornfeld, R. Steet, 2014, The Journal of Biological Chemistry.

The DMAP interaction domain of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase is a substrate recognition module

E. van Meel, S. Kornfeld, R. Steet, 2013, Proceedings of the National Academy of Sciences.

Multiple Domains of GlcNAc-1-phosphotransferase Mediate Recognition of Lysosomal Enzymes*

E. van Meel, S. Kornfeld, B. Doray, 2016, The Journal of Biological Chemistry.

Detection of Active Mammalian GH31 α-Glucosidases in Health and Disease Using In-Class, Broad-Spectrum Activity-Based Probes

G. A. van der Marel, G. Davies, J. Jiang, 2016, ACS central science.

Nicotiana benthamiana α-galactosidase A1.1 can functionally complement human α-galactosidase A deficiency associated with Fabry disease

M. Artola, N. Pannu, D. Bosch, 2018, The Journal of Biological Chemistry.

Tuberous sclerosis, polycystic kidney disease and mucolipidosis III gamma caused by a microdeletion unmasking a recessive mutation

L. Bird, E. van Meel, S. Kornfeld, 2015, American journal of medical genetics. Part A.

Exome sequencing for mucolipidosis III: Detection of a novel GNPTAB gene mutation in a patient with a very mild phenotype

J. Kitajima, E. van Meel, S. Kornfeld, 2014, Molecular genetics and metabolism reports.

hVps41 and VAMP7 function in direct TGN to late endosome transport of lysosomal membrane proteins

S. Mayor, Maaike Pols, J. Klumperman, 2013, Nature Communications.

Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype

P. Cliften, E. van Meel, S. Kornfeld, 2013, BMC Medical Genetics.

Autophagy proteins regulate the secretory component of osteoclastic bone resorption.

H. Virgin, W. Zou, S. Teitelbaum, 2011, Developmental cell.

Vacuolization of Mucolipidosis Type Ii Mouse Exocrine Gland Cells Represents Accumulation of Autolysosomes Recommended Citation Vacuolization of Mucolipidosis Type Ii Mouse Exocrine Gland Cells Represents Accumulation of Autolysosomes

E. van Meel, V. Oorschot, Marielle Boonen, 2022 .