Van Weely S - Search Results

1

Comparative study on glucocerebrosidase in spleens from patients with Gaucher disease.

Aerts JM, Donker-Koopman WE, Brul S, Van Weely S, Sa Miranda MC, Barranger JA, Tager JM, Schram AW. Aerts JM, et al. Among authors: van weely s. Biochem J. 1990 Jul 1;269(1):93-100. doi: 10.1042/bj2690093. Biochem J. 1990. PMID: 2198026 Free PMC article.

2

Clinical phenotype of Gaucher disease in relation to properties of mutant glucocerebrosidase in cultured fibroblasts.

Van Weely S, Van Leeuwen MB, Jansen ID, De Bruijn MA, Brouwer-Kelder EM, Schram AW, Sa Miranda MC, Barranger JA, Petersen EM, Goldblatt J, et al. Van Weely S, et al. Among authors: van leeuwen mb. Biochim Biophys Acta. 1991 Jun 5;1096(4):301-11. doi: 10.1016/0925-4439(91)90066-i. Biochim Biophys Acta. 1991. PMID: 1829642

3

The identification of type 1 Gaucher disease patients, asymptomatic cases and carriers in The Netherlands using urine samples: an evaluation.

Aerts JM, Sa Miranda MC, Wanzeller de Lacerda L, van Weely S, Donker-Koopman W, Brouwer-Kelder B, Jansen DC, van Leeuwen M, Schram AW, Tsiapara A, et al. Aerts JM, et al. Among authors: van leeuwen m, van weely s. Clin Chim Acta. 1991 Dec 16;203(2-3):349-61. doi: 10.1016/0009-8981(91)90308-y. Clin Chim Acta. 1991. PMID: 1838035

4

Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolase.

Van Weely S, Aerts JM, Van Leeuwen MB, Heikoop JC, Donker-Koopman WE, Barranger JA, Tager JM, Schram AW. Van Weely S, et al. Among authors: van leeuwen mb. Eur J Biochem. 1990 Aug 17;191(3):669-77. doi: 10.1111/j.1432-1033.1990.tb19173.x. Eur J Biochem. 1990. PMID: 2143986 Free article.

5

Conditions affecting the activity of glucocerebrosidase purified from spleens of control subjects and patients with type 1 Gaucher disease.

Aerts JM, Sa Miranda MC, Brouwer-Kelder EM, Van Weely S, Barranger JA, Tager JM. Aerts JM, et al. Among authors: van weely s. Biochim Biophys Acta. 1990 Oct 18;1041(1):55-63. doi: 10.1016/0167-4838(90)90122-v. Biochim Biophys Acta. 1990. PMID: 2223847

6

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. Among authors: van weely s. Biochim Biophys Acta. 1988 Mar 17;964(3):303-8. doi: 10.1016/0304-4165(88)90030-x. Biochim Biophys Acta. 1988. PMID: 3349099

7

Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cells.

Aerts JM, Heikoop J, van Weely S, Donker-Koopman WE, Barranger JA, Tager JM, Schram AW. Aerts JM, et al. Among authors: van weely s. Exp Cell Res. 1988 Aug;177(2):391-8. doi: 10.1016/0014-4827(88)90472-7. Exp Cell Res. 1988. PMID: 3391250

8

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. Among authors: van weely s. J Inherit Metab Dis. 1993;16(2):288-91. doi: 10.1007/BF00710267. J Inherit Metab Dis. 1993. PMID: 8411983 Review. No abstract available.

9

Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher disease.

van Weely S, van den Berg M, Barranger JA, Sa Miranda MC, Tager JM, Aerts JM. van Weely S, et al. Among authors: van den berg m. J Clin Invest. 1993 Mar;91(3):1167-75. doi: 10.1172/JCI116276. J Clin Invest. 1993. PMID: 8450045 Free PMC article.

10

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. Biochim Biophys Acta. 1993 Mar 24;1181(1):55-62. doi: 10.1016/0925-4439(93)90090-n. Biochim Biophys Acta. 1993. PMID: 8457606

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