Aerts JM - Search Results

1

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. Among authors: aerts jm. J Biol Chem. 1998 Oct 2;273(40):25680-5. doi: 10.1074/jbc.273.40.25680. J Biol Chem. 1998. PMID: 9748235 Free article.

2

Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylation.

Aerts JM, Schram AW, Strijland A, van Weely S, Jonsson LM, Tager JM, Sorrell SH, Ginns EI, Barranger JA, Murray GJ. Aerts JM, et al. Biochim Biophys Acta. 1988 Mar 17;964(3):303-8. doi: 10.1016/0304-4165(88)90030-x. Biochim Biophys Acta. 1988. PMID: 3349099

3

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. Among authors: aerts jm. J Biol Chem. 1995 Nov 3;270(44):26252-6. doi: 10.1074/jbc.270.44.26252. J Biol Chem. 1995. PMID: 7592832 Free article.

4

Purification and characterization of human chitotriosidase, a novel member of the chitinase family of proteins.

Renkema GH, Boot RG, Muijsers AO, Donker-Koopman WE, Aerts JM. Renkema GH, et al. Among authors: aerts jm. J Biol Chem. 1995 Feb 3;270(5):2198-202. doi: 10.1074/jbc.270.5.2198. J Biol Chem. 1995. PMID: 7836450 Free article.

5

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.

6

Demonstration of the existence of a second, non-lysosomal glucocerebrosidase that is not deficient in Gaucher disease.

van Weely S, Brandsma M, Strijland A, Tager JM, Aerts JM. van Weely S, et al. Among authors: aerts jm. Biochim Biophys Acta. 1993 Mar 24;1181(1):55-62. doi: 10.1016/0925-4439(93)90090-n. Biochim Biophys Acta. 1993. PMID: 8457606

7

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. Among authors: aerts jm. J Inherit Metab Dis. 1995;18(5):609-15. doi: 10.1007/BF02436006. J Inherit Metab Dis. 1995. PMID: 8598642

8

A case of type I Gaucher disease with cardiopulmonary amyloidosis and chitotriosidase deficiency.

Hrebícek M, Zeman J, Musilová J, Hodanová K, Renkema GH, Vepreková L, Ledvinová J, Hrebícek D, Sokolová J, Aerts JM, Elleder M. Hrebícek M, et al. Among authors: aerts jm. Virchows Arch. 1996 Nov;429(4-5):305-9. doi: 10.1007/BF00198347. Virchows Arch. 1996. PMID: 8972767

9

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. Among authors: aerts jm. 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 Free article.

10

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. Among authors: aerts jm. 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

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