(Q40267841)

19 September 2017

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title

Aspartylglycosaminuria: an inborn error of glycoprotein catabolism (English)

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19 September 2017

C P Maury

1

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19 September 2017

publication date

1 January 1982

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Journal of Inherited Metabolic Disease

19 September 2017

published in

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19 September 2017

volume

5

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19 September 2017

issue

4

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19 September 2017

page(s)

192-196

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Distribution, purification and properties of 1-aspartamido-beta-N-acetylglucosamine amidohydrolase

19 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

Measurement of 1-aspartamido-beta-N-acetylglucosamine amidohydrolase activity in human tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

Purification and some properties of 1-aspartamido-β-N-acetylglucosamine amidohydrolase from human liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

Glycoprotein catabolism in rat liver. Lysosomal digestion of iodinated asialo-fetuin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

Cytosolic location of an endo-N-acetyl-β-D-glucosaminidase activity in rat liver and kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

The glycoasparagines in urine of a patient with aspartylglycosaminuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

Isolation of the liver N-aspartyl-beta-glucosaminidase in aspartylglucosaminuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02179139

Structural determination of three glycoasparagines isolated from the urine of a patient with aspartylglycosaminuria

21 January 2018

1 reference

12 December 2020

Urinary sialic acid levels in aspartylglycosaminuria.

1 reference

12 December 2020

High-performance liquid chromatographic analysis of oligosaccharides and glycopeptides accumulating in lysosomal storage disorders

1 reference

12 December 2020

Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria

1 reference

12 December 2020

Identification of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in biological materials by gas chromatography-mass spectrometry

1 reference

12 December 2020

Distribution of cytoplasmic vacuoles in blood T and B lymphocytes in two lysosomal disorders

1 reference

12 December 2020

Aspartylglucosaminuria: Deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents

1 reference

12 December 2020

Isolation of 2-acetamido-1- -(L- -aspartamido)-1,2-dideoxy-D-glucose from normal human urine

1 reference

12 December 2020

Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.

1 reference

12 December 2020

Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU)

1 reference

12 December 2020

Endoglycosidases acting on carbohydrate moieties of glycoproteins: demonstration in mammalian tissue

1 reference

12 December 2020

Aspartylglycosaminuria. Analysis of thirty-four patients

1 reference

12 December 2020

Enzymatic determination of urinary aspartylglycosylamine: a rapid and sensitive-method to detect aspartylclycosylaminuria (AGU)

1 reference

12 December 2020

Detection of aspartylglycosaminuria by gas--liquid chromatography

1 reference

12 December 2020

N-Acetylglucosamine-asparagine levels in tissues of patients with aspartylglycosaminuria

1 reference

12 December 2020

Enzymatic Diagnosis and Carrier Detection of Aspartylglucosaminuria Using Blood Samples

1 reference

12 December 2020

The purification and properties of a beta-aspartyl N-acetylglucosylamine amidohydrolase from hen oviduct

1 reference

12 December 2020

Automated ion-exchange chromatography in the detection of aspartylglucosaminuria

1 reference

12 December 2020

Characterization of Two Glycoasparagines Isolated from the Urine of Patients with Aspartylglycosylaminuria (AGU)1

1 reference

12 December 2020

Accumulation of two glycoasparagines in the liver in aspartylglycosaminuria

1 reference

12 December 2020

Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria

1 reference

12 December 2020

Characterization of One Neutral and Two Acidic Glycoasparagines Isolated from the Urine of Patients with Aspartylglycosylaminuria (AGU)1

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12 December 2020

Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between english and finnish patients with special reference to storage materials

1 reference

12 December 2020

Thin-layer chromatographic demonstration of aspartylglycosylamine and a novel acidic carbohydrate in human tissues

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12 December 2020

Aspartylglucosaminuria II: biochemical studies on brain, liver, kidney and spleen

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12 December 2020

β-Aspartylglucosylamine Amido Hydrolase of Rat Liver and Kidney

1 reference

12 December 2020

Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies

1 reference

12 December 2020

Studies on N-aspartyl-β-glucosaminidase in aspartylglycosaminuria

1 reference

12 December 2020

Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patients

1 reference

12 December 2020

Distribution of a glycopeptide-degrading enzyme in tissue and cells.

1 reference

12 December 2020

Regional distribution of glycoasparagine storage material in the brain in aspartylglycosaminuria

1 reference

12 December 2020

Variation of urinary excretion of aspartylglucosamine and associated clinical findings in aspartyglucosaminuria

1 reference

12 December 2020

Structure of a carbohydrate moiety of a unit A glycopeptide of calf thyroglobulin

1 reference

12 December 2020

An improved thin-layer chromatographic method for urinary oligosaccharide screening

1 reference

12 December 2020

Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts

1 reference

12 December 2020

Eleven new cases of aspartylglucosaminuria

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12 December 2020

Enzymatic cleavage of glycopeptides

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12 December 2020

Quantitative determination of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in the urine of patients with aspartylglycosaminuria by gas-liquid chromatography

1 reference

12 December 2020

Enzymatic cleavage of 2-acetamido-1-(beta'-L-aspartamido)-1,2-dideoxy-beta-D-glucose by human plasma and seminal fluid. Failure to detect the heterozygous state for aspartylglycosaminuria

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02179139

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Dimensions Publication ID

19 September 2017

1029783699

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