Boot, Rolf G.

The Human Chitotriosidase Gene

Boot, R. G., Renkema, G. H., Verhoek, M., Strijland, A., Bliek, J., de Meulemeester, T. M. A. M. O., Mannens, M. M. A. M., & Aerts, J. M. F. G. (1998) · Journal of Biological Chemistry

Studies on Chitinases and ChitosanasesLysosomal Storage Disorders Research

Cited by 416

Myelin-laden macrophages are anti-inflammatory, consistent with foam cells in multiple sclerosis

Boven, L. A., Van Meurs, M., Van Zwam, M., Wierenga-Wolf, A., Hintzen, R. Q., Boot, R. G., Aerts, J. M., Amor, S., Nieuwenhuis, E. E., & Laman, J. D. (2006) · Brain

Multiple Sclerosis Research StudiesNeuroinflammation and Neurodegeneration Mechanisms

Cited by 353

Plasma chitotriosidase and CCL18: Early biochemical surrogate markers in type B Niemann‐Pick disease

Brinkman, J., Wijburg, F. A., Hollak, C. E., Groener, J. E., Verhoek, M., Scheij, S., Aten, J., Boot, R. G., & Aerts, J. M. (2005) · Journal of Inherited Metabolic Disease

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 90

Glycoprotein Non-Metastatic Protein B: An Emerging Biomarker for Lysosomal Dysfunction in Macrophages

Van der Lienden, M. J. C., Gaspar, P., Boot, R., Aerts, J. M. F. G., & Van Eijk, M. (2018) · International Journal of Molecular Sciences

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 84

Value of plasma chitotriosidase to assess non‐neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapy

van Dussen, L., Hendriks, E. J., Groener, J. E. M., Boot, R. G., Hollak, C. E. M., & Aerts, J. M. F. G. (2014) · Journal of Inherited Metabolic Disease

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 78