Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical and immunological study (Q68324709)

From Wikidata

Jump to navigation Jump to search

scientific article published on 01 June 1991

Language	Label	Description	Also known as
English	Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical and immunological study	scientific article published on 01 June 1991

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological study (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical and immunological study (English)

1 reference

10.1007/BF02072213

https://api.crossref.org/works/10.1007/BF02072213

28 October 2022

1 reference

based on heuristic

inferred from title

author name string

W. Schlote

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

K. Harzer

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

H. Christomanou

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

B. C. Paton

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

B. Kustermann-Kuhn

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

B. Schmid

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

J. Seeger

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

U. Beudt

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

I. Schuster

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

U. Langenbeck

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683286

28 October 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1683286

28 October 2022

publication date

1 June 1991

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF02072213.pdf

Portable Document Format

1 reference

10.1007/BF02072213

https://api.crossref.org/works/10.1007/BF02072213

28 October 2022

http://link.springer.com/article/10.1007/BF02072213/fulltext.html

1 reference

10.1007/BF02072213

https://api.crossref.org/works/10.1007/BF02072213

28 October 2022

http://link.springer.com/content/pdf/10.1007/BF02072213

1 reference

10.1007/BF02072213

https://api.crossref.org/works/10.1007/BF02072213

28 October 2022

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

150

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

584-591

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incorporation and metabolism of ganglioside GM2 in skin fibroblasts from normal and GM2 gangliosidosis subjects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunocytochemical localization of sphingolipid activator protein-1, the sulfatide/GM1 ganglioside activator, to lysosomes in human liver and colon

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A variant form of metachromatic leukodystrophy without arylsulfatase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activator protein deficient Gaucher's disease. A second patient with the newly identified lipid storage disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

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/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide sequence of cloned cDNA for human sphingolipid activator protein 1 precursor

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

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/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of full-length cDNA coding for sulfatide activator, a Co-beta-glucosidase and two other homologous proteins: two alternate forms of the sulfatide activator

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

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/1683286

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/1683286

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/1683286

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/1683286

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/1683286

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/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The assay of arylsulphatases A and B in human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete amino-acid sequence of the naturally occurring A2 activator protein for enzymic sphingomyelin degradation: identity to the sulfatide activator protein (SAP-1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for two different active sites on human beta-hexosaminidase A. Interaction of GM2 activator protein with beta-hexosaminidase A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activator proteins for lysosomal glycolipid hydrolysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

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/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunocytochemical localization of sphingolipid activator protein 2 (SAP-2) in normal and SAP-deficient fibroblasts.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a cDNA encoding the human GM2 activator protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activator protein-deficient metachromatic leukodystrophy: diagnosis in leukocytes using immunologic methods

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis and processing of sphingolipid activator protein-2 (SAP-2) in cultured human fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, pathological, and biochemical studies on an infantile case of sulfatide/GM1 activator protein deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

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/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical, immunological, and structural studies on a sphingolipid activator protein (SAP-1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of a point mutation in sphingolipid activator protein-1 mRNA in patients with a variant form of metachromatic leukodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insertion in the mRNA of a metachromatic leukodystrophy patient with sphingolipid activator protein-1 deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isoelectric Focusing Pattern of Acid Hydrolases in Cultured Fibroblasts, Leucocytes and Cell-Free Amniotic Fluid

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1683286

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/1683286

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease

10

1 reference

10.1007/BF02072213

https://api.crossref.org/works/10.1007/BF02072213

28 October 2022

Identifiers

10.1007/BF02072213

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683286%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q68324709&oldid=2218523907"