(Q38241614)

English

Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses

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scholarly article

1 reference

Europe PubMed Central

31 August 2017

1 reference

Europe PubMed Central

Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses (English)

1 reference

Europe PubMed Central

31 August 2017

1 reference

based on heuristic

inferred from title

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inferred from title

protein deficiency

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based on heuristic

inferred from title

Gaucher's disease

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author name string

K Harzer

1

1 reference

Europe PubMed Central

31 August 2017

B C Paton

2

1 reference

Europe PubMed Central

31 August 2017

A Poulos

3

1 reference

Europe PubMed Central

31 August 2017

B Kustermann-Kuhn

4

1 reference

Europe PubMed Central

31 August 2017

W Roggendorf

5

1 reference

Europe PubMed Central

31 August 2017

T Grisar

6

1 reference

Europe PubMed Central

31 August 2017

M Popp

7

1 reference

Europe PubMed Central

31 August 2017

language of work or name

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inferred from title

publication date

1 October 1989

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Europe PubMed Central

31 August 2017

European Journal of Pediatrics

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Europe PubMed Central

31 August 2017

149

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Europe PubMed Central

31 August 2017

1

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Europe PubMed Central

31 August 2017

31-39

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Europe PubMed Central

31 August 2017

https://scigraph.springernature.com/pub.10.1007/bf02024331

0 references

The activator of cerebroside-sulphatase. A model of the activation

1 reference

https://api.crossref.org/works/10.1007%2FBF02024331

21 January 2018

Analysis of the multiple forms of Gaucher spleen sphingolipid activator protein 2.

1 reference

https://api.crossref.org/works/10.1007%2FBF02024331

21 January 2018

Studies on the activation of the enzymatic hydrolysis of sphingomyelin liposomes.

1 reference

https://api.crossref.org/works/10.1007%2FBF02024331

21 January 2018

Preliminary evidence for a processing error in the biosynthesis of Gaucher activator in mucolipidosis disease types II and III.

1 reference

https://api.crossref.org/works/10.1007%2FBF02024331

21 January 2018

An endogenous activator protein in human placenta for enzymatic degradation of glucosylceramide

1 reference

https://api.crossref.org/works/10.1007%2FBF02024331

21 January 2018

A protein activator of galactosylceramide beta-galactosidase.

1 reference

https://api.crossref.org/works/10.1007%2FBF02024331

21 January 2018

Studies on a sphingolipid activator protein (SAP-2) in fibroblasts from patients with lysosomal storage diseases, including Niemann-Pick disease Type C

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cerebrosidesulfatase from swine kidney

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neurological Gaucher's disease in three siblings. An ultrastructural study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolism of fatty acid-labeled cerebroside sulfate in cultured cells from controls and metachromatic leukodystrophy patients. Use in the prenatal identification of a false positive fetus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Farber's disease in two siblings, sural nerve and subcutaneous biopsies by light and electron microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The precursor of sulfatide activator protein is processed to three different proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Letters: A simple sphingomyelinase determination for Niemann-Pick disease: differential diagnosis of types A, B and C.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complexing of Glycolipids and Their Transfer between Membranes by the Activator Protein for Degradation of Lysosomal Ganglioside GM2

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identity of the activator proteins for the enzymatic hydrolysis of sulfatide, ganglioside GM1, and globotriaosylceramide

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the gene for human sphingolipid activator protein-2 (SAP-2) to chromosome 10.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coding of two sphingolipid activator proteins (SAP-1 and SAP-2) by same genetic locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and properties of a heat-stable glucocerebrosidase activating factor from control and Gaucher spleen

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunochemical characterization of two activator proteins stimulating enzymic sphingomyelin degradation in vitro. Absence of one of them in a human Gaucher disease variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of two forms of an activator protein for the enzymic sphingomyelin degradation from human Gaucher spleen

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The binding of glucosylceramidase to glucosylceramide is promoted by its activator protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metachromatic leukodystrophy without arylsulfatase A deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

beta-Glucosidase activator protein from bovine spleen ("coglucosidase")

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activator protein required for the enzymatic hydrolysis of cerebroside sulfate. Deficiency in urine of patients affected with cerebroside sulfatase activator deficiency and identity with activators for the enzymatic hydrolysis of GM1 ganglioside and

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of combined Farber and Sandhoff disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal enzymic diagnosis in 24 pregnancies with risk of Krabbe disease .

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presence of activator proteins for the enzymatic degradation of glucosylceramide in several human tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

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/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of metachromatic leukodystrophy, Krabbe disease, and Farber disease after uptake of fatty acid-labeled cerebroside sulfate into cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cohydrolases in human spleen that stimulate glucosyl ceramide beta-glucosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene coding for a sphingolipid activator protein, SAP-1, is on human chromosome 10

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specificity of low molecular weight glycoprotein effector of lipid glycosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and Characterization of an Activator Protein for the Degradation of Glycolipids GM2and GA2by Hexosaminidase A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of activation of glucocerebrosidase by CO-β-glucosidase (glucosidase activator protein)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymic diagnosis in 27 cases with Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2514102

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02024331

1 reference

Europe PubMed Central

31 August 2017

Dimensions Publication ID

0 references

release_jmoffc77rzejvpsooam375jbbe

1 reference

https://api.fatcat.wiki/v0/release/jmoffc77rzejvpsooam375jbbe

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

31 August 2017

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