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Scandinavian Journal of Clinical and Laboratory Investigation Volume 48, 1988 - Issue sup191
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Original Article

Laboratory detection of aspartylglycosaminuria

I. Mononen Department of Clinical Chemistry, Kuopio University Central Hospital, SF-70210, Kuopio, Finland
,
V. Kaartinen Department of Clinical Chemistry, Kuopio University Central Hospital, SF-70210, Kuopio, Finland
&
T. Mononen Department of Clinical Chemistry, Kuopio University Central Hospital, SF-70210, Kuopio, Finland
Pages 7-11 | Published online: 17 Mar 2010

Citations (6)

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John M. Risley, De Hua Huang, Jerry J. Kaylor, Jayshri J. Malik & Yuan-Qing Xia. (2001) Glycosylasparaginase Inhibition Studies: Competitive Inhibitors, Transition State Mimics, Noncompetitive Inhibitors. Journal of Enzyme Inhibition 16:3, pages 269-274.
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Articles from other publishers (5)

Antje Banning, Minna Laine & Ritva Tikkanen. (2023) Validation of Aspartylglucosaminidase Activity Assay for Human Serum Samples: Establishment of a Biomarker for Diagnostics and Clinical Studies. International Journal of Molecular Sciences 24:6, pages 5722.
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Maria Arvio & Ilkka Mononen. (2016) Aspartylglycosaminuria: a review. Orphanet Journal of Rare Diseases 11:1.
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Vesa Kaartinen. (1991) Glycoasparaginase in human urine. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1097:1, pages 28-30.
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K.J. Fisher & N.N. AronsonJr.Jr.. (1991) Characterization of the mutation responsible for aspartylglucosaminuria in three Finnish patients. Amino acid substitution Cys163—-Ser abolishes the activity of lysosomal glycosylasparaginase and its conversion into subunits. Journal of Biological Chemistry 266:18, pages 12105-12113.
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V. Kaartinen & I. Mononen. (1990) Assay of aspartylglycosylaminase by high-performance liquid chromatography. Analytical Biochemistry 190:1, pages 98-101.
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