(Q70159079)

English

Selective depolymerisation of heparin to produce radio-labelled substrates for sulfamidase, 2-acetamido-2-deoxy-alpha-D-glucosidase, acetyl-CoA:2-amino-2-deoxy-alpha-D-glucoside N-acetyltransferase, and 2-acetamido-2-deoxy-D-glucose 6-sulfate sulfat

scientific article published on 01 May 1981

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7018684%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

Selective depolymerisation of heparin to produce radio-labelled substrates for sulfamidase, 2-acetamido-2-deoxy-alpha-D-glucosidase, acetyl-CoA:2-amino-2-deoxy-alpha-D-glucoside N-acetyltransferase, and 2-acetamido-2-deoxy-D-glucose 6-sulfate sulfatase (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7018684%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

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J J Hopwood

1

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9 October 2019

H Elliott

2

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9 October 2019

publication date

1 May 1981

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9 October 2019

Carbohydrate Research

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7018684%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

91

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9 October 2019

2

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9 October 2019

165-190

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PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7018684%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

The mucopolysaccharidoses (a review).

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Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation

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Sanfilippo syndrome type C: deficiency of acetyl-CoA:alpha-glucosaminide N-acetyltransferase in skin fibroblasts

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Ganglioside catabolism in hexosaminidase A-deficient adults.

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Neuropathic Gaucher's disease with normal 4-methylumbelliferyl-beta-glucosidase activity in the liver

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Pitfalls in the use of artificial substrates for the diagnosis of Gaucher's disease

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Biochemical Discrimination of Hurler and Scheie Syndromes

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An assay for iduronate sulfatase (Hunter corrective factor)

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A radioactive substrate and assay for α-l-iduronidase

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Substrates for the assay of alpha-L-iduronidase

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α-l-Iduronidase, β-d-glucuronidase, and 2-sulfo-l-iduronate 2-sulfutase: preparation and characterization of radioactive substrates from heparin

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Post- and Pre-Natal Assessment of α-l-Iduronidase Deficiency with a Radiolabelled Natural Substrate

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7 January 2021

A fluorometric assay using 4-methylumbelliferyl α-l-iduronide for the estimation of α-l-iduronidase activity and the detection of Hurler and Scheie syndromes

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7 January 2021

Identification of N-sulphated disaccharide units in heparin-like polysaccharides

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7 January 2021

Nearest neighbor analysis of heparin: identification and quantitation of the products formed by selective depolymerization procedures

1 reference

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7 January 2021

Formation of anhydrosugars in the chemical depolymerization of heparin

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7 January 2021

The Distribution of Sulfated Uronic Acid and Hexosamine Residues in Heparin and Heparan Sulfate

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7 January 2021

Structural characteristics of heparan sulfates with varying sulfate contents

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7 January 2021

Glycosaminoglycans and Their Binding to Biological Macromolecules

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7 January 2021

Anticoagulant activity of heparin: isolation of antithrombin-binding sites

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7 January 2021

Structure-function relationships of heparin species

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7 January 2021

Qualitative and quantitative analysis of reducing carbohydrates by radiochromatography on ion-exchange papers.

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7 January 2021

A modified uronic acid carbazole reaction

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Studies on yeast metabolism. I. Fractionation and microdetermination of cell carbohydrates

1 reference

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7 January 2021

Stoichiometric depolymerization of polyuronides and glycosaminoglycuronans to monosaccharides following reduction of their carbodiimide-activated carboxyl groups

1 reference

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7 January 2021

Studies on heparin degradation. I. Preparation of ( 35 S) sulphamate derivatives for studies on heparin degrading enzymes of mammalian origin

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7 January 2021

The laboratory diagnosis of sanfilippo disease

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Sanfilippo B disease: serum assays for detection of homozygous and heterozygous individuals in three families

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The enzymic defect in Morquio's disease: The specificity of N-acetylhexosamine sulfatases

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7 January 2021

Ganglioside GM2 N-acetyl-ß-D-gafactosaminidase and asialo GM2 (GA2) N-acetyl-ß-D-galactosaminidase; studies in human skin fibroblasts

1 reference

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7 January 2021

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Variability of fibroblast lysosomal acid hydrolases with reference to the detection of enzyme deficiencies

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7 January 2021

based on heuristic

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Identifiers

10.1016/S0008-6215(00)86029-2

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7018684%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7018684%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

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