(Q28290426)

English

Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase

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scholarly article

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Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase (English)

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author name string

A Daniele

1

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P Di Natale

2

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language of work or name

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publication date

March 1987

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75

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3

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234-8

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Isolation of mammalian cell mutants deficient in glucose-6-phosphate dehydrogenase activity: linkage to hypoxanthine phosphoribosyl transferase

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https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

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Identification and partial characterization of two enzyme forms of iduronate sulfatase from human placenta.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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Morquio's disease type A: Absence of material cross reacting with antibodies against N-acetylgalactosamine-6-sulfate sulfatase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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Human hepatocellular carcinoma cell lines secrete the major plasma proteins and hepatitis B surface antigen

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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Biosynthesis and maturation of arylsulfatase B in normal and mutant cultured human fibroblasts.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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Iduronate sulfatase from human plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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based on heuristic

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Processing of human beta-galactosidase in GM1-gangliosidosis and Morquio B syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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Multiple forms of iduronate 2-sulphate sulphatase in human tissues and body fluids.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

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based on heuristic

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46 Enzymic diagnosis of the genetic mucopolysaccharide storage disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

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Iduronate sulfatase from human placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human beta-glucuronidase deficiency mucopolysaccharidosis: identification of cross-reactive antigen in cultured fibroblasts of deficient patients by enzyme immunoassay

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hunter's syndrome: a deficiency of L-idurono-sulfate sulfatase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sanfilippo disease type B: presence of material cross reacting with antibodies against alpha-N-acetylglucosaminidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein measurement with the Folin phenol reagent

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polyclonal antibodies against iduronate 2-sulphate sulphatase from human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3104200

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00281065

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release_czv3fspm7bdhlo44egws5dlvy4

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PubMed publication ID

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