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The Journal of Biological Chemistry|November 3, 1995
Cloning of a cDNA encoding chitotriosidase, a human chitinase produced by macrophagesR G Boot, G H Renkema, A Strijland, et al.Frontiers in Cell and Developmental Biology|December 24, 2019
Glycosphingolipids and Infection. Potential New Therapeutic AvenuesJohannes M F G Aerts, M Artola, M van Eijk, et al.The Journal of Biological Chemistry|February 3, 1995
Purification and characterization of human chitotriosidase, a novel member of the chitinase family of proteinsG H Renkema, R G Boot, A O Muijsers, et al.Journal of Inherited Metabolic Disease|January 1, 1995
Characterization of glucocerebrosidase in Greek Gaucher disease patients: mutation analysis and biochemical studiesH Michelakakis, E Dimitriou, S Van Weely, et al.Nederlands Tijdschrift Voor Geneeskunde|October 15, 2005
[From gene to disease; Gaucher disease]C E M Hollak, R G Boot, B J H M Poorthuis, et al.Expert Opinion on Investigational Drugs|October 15, 2010
Pharmacological small molecules for the treatment of lysosomal storage disordersB E Smid, J M F G Aerts, R G Boot, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
Identification and use of biomarkers in Gaucher disease and other lysosomal storage diseasesJ M F G Aerts, C E M Hollak, M van Breemen, et al.Journal of Inherited Metabolic Disease|May 17, 2014
Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapyL van Dussen, E J Hendriks, J E M Groener, et al.The Journal of Biological Chemistry|September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiencyR G Boot, G H Renkema, M Verhoek, et al.The Journal of Biological Chemistry|November 22, 2000
Identification of a novel acidic mammalian chitinase distinct from chitotriosidaseR G Boot, E F Blommaart, E Swart, et al.Pageof 2