L-Aspartic acid-β-7-amido-4-methylcoumarin is a sensitive and specific fluorogenic substrate for lysosomal glycoasparaginase (aspartylgluco-saminidase). Fibroblasts and leukocytes from 8 patients with aspartylglucosaminuria, showed 1-7% of the mean normal glycoasparaginase activity. Heterozygotes showed intermediate activities. Glycoasparaginase activity in chorionic villi, cultured trophoblasts, cultured amniotic fluid cells and amniotic fluid was readily detectable, indicating that prenatal analysis of aspartylglucosaminuria should be possible with this assay. β-Aspartyl-4-methylumbelliferone was synthesized but this potential substrate can not be used to assay glycoasparaginase since it hydrolyses spontaneously
L-asparaginase (ASNase) is an aminohydrolase enzyme widely used in the pharmaceutical and food indus...
Background: Mucopolysaccharidosis type IVA, also known as Morquio A or MPS IV A, is an autosomal rec...
Bei der Aspartylglukosaminurie handelt es sich um eine lysosomale Speicherkrankheit. Die Mutationen ...
textabstractL-Aspartic acid-β-7-amido-4-methylcoumarin is a sensitive and specific fluorogenic subst...
A new fluorogenic substrate, 4 methylumbelliferyl B-D-6-sulphogalactoside, was used for the assay o...
Serum, plasma, and lymphocytes from aspartyiglycosami-nuria (AGU) patients and carriers and from nor...
We report on the development of a sensitive real-time assay for monitoring the activity of L-asparag...
Aspartylglucosaminuria (AGU), a recessively inherited lysosomal storage disease, is the most common ...
4-Methylumbelliferyl-α-N-acetylglucosamine 6-sulphate was synthesized and shown to be a substrate fo...
Immunogenicity is one of the most common complications occurring during therapy making use of protei...
A rapid and sensitive method to quantitatively assess N-acetylglucosaminidase (NAG) activity in cult...
AbstractGlycosylasparaginase is a lysosomal amidase involved in the degradation of glycoproteins. Re...
The apparent active site of human leukocyte glycoasparaginase (N4-(beta-acetylglucosaminyl)-L-aspara...
This study deals with different aspects of asparagine metabolism. First, a highly sensitive method f...
Aspartylglucosaminuria (AGU) is a lysosomal storage disorder that is caused by genetic deficiency of...
L-asparaginase (ASNase) is an aminohydrolase enzyme widely used in the pharmaceutical and food indus...
Background: Mucopolysaccharidosis type IVA, also known as Morquio A or MPS IV A, is an autosomal rec...
Bei der Aspartylglukosaminurie handelt es sich um eine lysosomale Speicherkrankheit. Die Mutationen ...
textabstractL-Aspartic acid-β-7-amido-4-methylcoumarin is a sensitive and specific fluorogenic subst...
A new fluorogenic substrate, 4 methylumbelliferyl B-D-6-sulphogalactoside, was used for the assay o...
Serum, plasma, and lymphocytes from aspartyiglycosami-nuria (AGU) patients and carriers and from nor...
We report on the development of a sensitive real-time assay for monitoring the activity of L-asparag...
Aspartylglucosaminuria (AGU), a recessively inherited lysosomal storage disease, is the most common ...
4-Methylumbelliferyl-α-N-acetylglucosamine 6-sulphate was synthesized and shown to be a substrate fo...
Immunogenicity is one of the most common complications occurring during therapy making use of protei...
A rapid and sensitive method to quantitatively assess N-acetylglucosaminidase (NAG) activity in cult...
AbstractGlycosylasparaginase is a lysosomal amidase involved in the degradation of glycoproteins. Re...
The apparent active site of human leukocyte glycoasparaginase (N4-(beta-acetylglucosaminyl)-L-aspara...
This study deals with different aspects of asparagine metabolism. First, a highly sensitive method f...
Aspartylglucosaminuria (AGU) is a lysosomal storage disorder that is caused by genetic deficiency of...
L-asparaginase (ASNase) is an aminohydrolase enzyme widely used in the pharmaceutical and food indus...
Background: Mucopolysaccharidosis type IVA, also known as Morquio A or MPS IV A, is an autosomal rec...
Bei der Aspartylglukosaminurie handelt es sich um eine lysosomale Speicherkrankheit. Die Mutationen ...