(Q68214116)

English

Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disorders

scientific article published on 01 July 1992

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634229%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disorders (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634229%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference

based on heuristic

inferred from title

1 reference

10.1007/BF00219176

https://api.crossref.org/works/10.1007/BF00219176

18 October 2022

author name string

B. Schmid

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1634229

18 October 2022

B. C. Paton

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1634229

18 October 2022

K. Sandhoff

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1634229

18 October 2022

K. Harzer

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1634229

18 October 2022

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1634229

18 October 2022

publication date

1 July 1992

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634229%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00219176.pdf

Portable Document Format

1 reference

10.1007/BF00219176

https://api.crossref.org/works/10.1007/BF00219176

18 October 2022

http://link.springer.com/article/10.1007/BF00219176/fulltext.html

1 reference

10.1007/BF00219176

https://api.crossref.org/works/10.1007/BF00219176

18 October 2022

http://link.springer.com/content/pdf/10.1007/BF00219176

1 reference

10.1007/BF00219176

https://api.crossref.org/works/10.1007/BF00219176

18 October 2022

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634229%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

89

1 reference

Europe PubMed Central

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22 September 2019

5

1 reference

Europe PubMed Central

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22 September 2019

513-518

1 reference

Europe PubMed Central

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22 September 2019

https://scigraph.springernature.com/pub.10.1007/bf00219176

0 references

Incorporation and degradation of GM1 ganglioside and asialoGM1 ganglioside in cultured fibroblasts from normal individuals and patients with beta-galactosidase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human acid beta-glucosidase. Use of inhibitory and activating monoclonal antibodies to investigate the enzyme's catalytic mechanism and saposin A and C binding sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The complete amino-acid sequences of human ganglioside GM2 activator protein and cerebroside sulfate activator protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Saposin A: second cerebrosidase activator protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ganglioside GM1 metabolism in living human fibroblasts with beta-galactosidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

B1 variant of GM2 gangliosidosis in a 12-year-old patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The accumulation of cerebroside sulfates by fibroblasts in culture from patients with late infantile metachromatic leukocystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A protein activator of galactosylceramide beta-galactosidase.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Saposin proteins: structure, function, and role in human lysosomal storage disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

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/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ganglioside GM3 sialidase activity in fibroblasts of normal individuals and of patients with sialidosis and mucolipidosis IV. Subcellular distribution and and some properties

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

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/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Saposin D: a sphingomyelinase activator

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sulfatide activator protein. Alternative splicing that generates three mRNAs and a newly found mutation responsible for a clinical disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a nonspecific activator protein for the enzymatic hydrolysis of glycolipids

1 reference

https://pubmed.ncbi.nlm.nih.gov/1634229

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00219176

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634229%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634229%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

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