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Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapy.
van Dussen L, Hendriks EJ, Groener JE, Boot RG, Hollak CE, Aerts JM. van Dussen L, et al. J Inherit Metab Dis. 2014 Nov;37(6):991-1001. doi: 10.1007/s10545-014-9711-x. Epub 2014 May 16. J Inherit Metab Dis. 2014. PMID: 24831585
Cloning of a cDNA encoding chitotriosidase, a human chitinase produced by macrophages.
Boot RG, Renkema GH, Strijland A, van Zonneveld AJ, Aerts JM. Boot RG, et al. J Biol Chem. 1995 Nov 3;270(44):26252-6. doi: 10.1074/jbc.270.44.26252. J Biol Chem. 1995. PMID: 7592832
Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease.
Aerts JM, Van Weely S, Boot R, Hollak CE, Tager JM. Aerts JM, et al. J Inherit Metab Dis. 1993;16(2):288-91. doi: 10.1007/BF00710267. J Inherit Metab Dis. 1993. PMID: 8411983 Review. No abstract available.
Characterization of glucocerebrosidase in Greek Gaucher disease patients: mutation analysis and biochemical studies.
Michelakakis H, Dimitriou E, Van Weely S, Boot RG, Mavridou I, Verhoek M, Aerts JM. Michelakakis H, et al. J Inherit Metab Dis. 1995;18(5):609-15. doi: 10.1007/BF02436006. J Inherit Metab Dis. 1995. PMID: 8598642
Synthesis, sorting, and processing into distinct isoforms of human macrophage chitotriosidase.
Renkema GH, Boot RG, Strijland A, Donker-Koopman WE, van den Berg M, Muijsers AO, Aerts JM. Renkema GH, et al. Eur J Biochem. 1997 Mar 1;244(2):279-85. doi: 10.1111/j.1432-1033.1997.00279.x. Eur J Biochem. 1997. PMID: 9118991
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value.
Boot RG, Hollak CE, Verhoek M, Sloof P, Poorthuis BJ, Kleijer WJ, Wevers RA, van Oers MH, Mannens MM, Aerts JM, van Weely S. Boot RG, et al. Hum Mutat. 1997;10(5):348-58. doi: 10.1002/(SICI)1098-1004(1997)10:5<348::AID-HUMU3>3.0.CO;2-B. Hum Mutat. 1997. PMID: 9375849
Chitotriosidase, a chitinase, and the 39-kDa human cartilage glycoprotein, a chitin-binding lectin, are homologues of family 18 glycosyl hydrolases secreted by human macrophages.
Renkema GH, Boot RG, Au FL, Donker-Koopman WE, Strijland A, Muijsers AO, Hrebicek M, Aerts JM. Renkema GH, et al. Eur J Biochem. 1998 Jan 15;251(1-2):504-9. doi: 10.1046/j.1432-1327.1998.2510504.x. Eur J Biochem. 1998. PMID: 9492324
The human chitotriosidase gene. Nature of inherited enzyme deficiency.
Boot RG, Renkema GH, Verhoek M, Strijland A, Bliek J, de Meulemeester TM, Mannens MM, Aerts JM. Boot RG, et al. J Biol Chem. 1998 Oct 2;273(40):25680-5. doi: 10.1074/jbc.273.40.25680. J Biol Chem. 1998. PMID: 9748235
Following the cloning of the chitotriosidase cDNA (Boot, R. G., Renkema, G. H., Strijland, A., van Zonneveld, A. J., and Aerts, J. ...
Following the cloning of the chitotriosidase cDNA (Boot, R. G., Renkema, G. H., Strijland, A., van Zonneveld, A. J., and Aerts, J. .. …
Strong induction of members of the chitinase family of proteins in atherosclerosis: chitotriosidase and human cartilage gp-39 expressed in lesion macrophages.
Boot RG, van Achterberg TA, van Aken BE, Renkema GH, Jacobs MJ, Aerts JM, de Vries CJ. Boot RG, et al. Arterioscler Thromb Vasc Biol. 1999 Mar;19(3):687-94. doi: 10.1161/01.atv.19.3.687. Arterioscler Thromb Vasc Biol. 1999. PMID: 10073974
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