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J.M.F.G Aerts

Veröffentlichungen von J.M.F.G Aerts zu van Weely, S. ->
weitere Veröffentlichungen von J.M.F.G Aerts:
Temperature-dependent lipid content and fatty acid composition of three thermophilic bacteria (1985)
Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease (1993)
Signals on proteins, intracellular targeting and inborn errors of organellar metabolism (1994)
The effect of enzyme therapy in a patient with Gaucher disease type III (1996)
Incorrect assignment of N370S mutation status by mismatched PCR/RFLP method in two Gaucher patients (1997)
Characterization of glucocerebrosidase in Greek Gaucher disease patients: mutation analysis and biochemical studies (1995)
Demonstration of the existence of a second, non-lysosomal glucocerebrosidase that is not deficient in Gaucher disease (1993)
A case of type I Gaucher disease with cardiopulmonary amyloidosis and chitotriosidase deficiency (1996)
Conditions affecting the activity of glucocerebrosidase purified fom spleens of control subjects and patients with type 1 Gaucher disease (1990)
Deficient activity of glucocerebrosidase in urine from patients with type 1 Gaucher disease (1986)
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies (1986)
An immunoelectron microscopic study of gluccereberosidase in type I Gaucher's disease spleen (1988)
Elevated plasma chitotriosidase activity in various lysosomal storage disorders (1995)
Oligosaccharide excretion in adult Gaucher disease (1998)
Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formation (1986)
Veröffentlichungen zu van Weely, S.
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1
van Weely, S., Brandsma, M., ... Demonstration of the existence of a second, non-lysosomal glucocerebrosidase that is not deficient in Gaucher disease
in: Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease, in: Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease . - Amsterdam : Elsevier, ISSN 0925-4439, ZDB-ID 2209528-7 Vol. 1181, No. 1 (1993), p. 55-62
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1993
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2
Aerts, J.M.F.G., Sa Miranda, M.C., ... Conditions affecting the activity of glucocerebrosidase purified fom spleens of control subjects and patients with type 1 Gaucher disease
in: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular, in: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular . - Amsterdam : Elsevier, ISSN 0167-4838, ZDB-ID 2209539-1 Vol. 1041, No. 1 (1990), p. 55-63
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1990
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3
de Jong, J. G. N., Aerts, J. M. F. G., ... Oligosaccharide excretion in adult Gaucher disease
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (1. 1998), p. 49-59
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1998
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4
Poorthuis, B.J.H.M., Wevers, R.A., ... The frequency of lysosomal storage diseases in The Netherlands
in: Human genetics , ISSN 1432-1203, Vol. 105 (1/2. 1999), p. 151-156
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1999
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5
Aerts, J.M.F.G., Brul, S., ... Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formation
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 141, No. 2 (1986), p. 452-458
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1986
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6
Aerts, J.M.F.G., Schram, A., ... Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylation
in: Biochimica et Biophysica Acta (BBA)/General Subjects, in: Biochimica et Biophysica Acta (BBA)/General Subjects . - Amsterdam : Elsevier, ISSN 0304-4165, ZDB-ID 2209617-6 Vol. 964, No. 3 (1988), p. 303-308
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1988
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7
Aerts, J.M.F.G., Brul, S., ... Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formation
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 141, No. 2 (1986), p. 452-458
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1986
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8
Aerts, J.M.F.G., Heikoop, J., ... Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cells
in: Experimental Cell Research, in: Experimental Cell Research . - Amsterdam : Elsevier, ISSN 0014-4827, ZDB-ID 1466780-0 Vol. 177, No. 2 (1988), p. 391-398
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1988
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9
Aerts, J.M.F.G., Miranda, M.C.S., ... The identification of type 1 Gaucher disease patients, asymptomatic cases and carriers in The Netherlands using urine samples: An evaluation
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 203, No. 2-3 (1991), p. 349-361
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1991
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10
Van Weely, S., Van Leeuwen, M.B., ... Clinical phenotype of Gaucher disease in relation to properties of mutant glucocerebrosidase in cultured fibroblasts
in: Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease, in: Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease . - Amsterdam : Elsevier, ISSN 0925-4439, ZDB-ID 2209528-7 Vol. 1096, No. 4 (1991), p. 301-311
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1991