(Q55044639)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Secondary sphingolipid accumulation in a macrophage model of Gaucher disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

0 references

1 reference

1 reference

Leanne K Hein

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Maria Fuller

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

18 September 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

7 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

336-345

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE.

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Gaucher's Disease in an Asymptomatic 72-Year-Old

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

The distribution of glucocerebroside in the liver of patients with Gaucher's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

The pathogenesis of glycosphingolipid storage disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Glucosylceramide modulates membrane traffic along the endocytic pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Cholesterol modulates membrane traffic along the endocytic pathway in sphingolipid-storage diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Glycosphingolipids are required for sorting melanosomal proteins in the Golgi complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Phosphatidylcholine metabolism is altered in a monocyte-derived macrophage model of Gaucher disease but not in lymphocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Glucosylceramide and glucosylsphingosine modulate calcium mobilization from brain microsomes via different mechanisms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Gaucher disease: pathological mechanisms and modern management

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Human leukocyte acid hydrolases: Characterization of eleven lysosomal enzymes and study of reaction conditions for their automated analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Studies on glucosaminidase. 4. The fluorimetric assay of N-acetyl-beta-glucosaminidase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Rat liver 5'-nucleotidase.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Genetic diseases of sphingolipid metabolism: pathological mechanisms and therapeutic options

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Intracellular trafficking of sphingolipids: relationship to biosynthesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Aminopropyl solid phase extraction and 2 D TLC of neutral glycosphingolipids and neutral lysoglycosphingolipids

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Regulation of ceramide production and apoptosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Phosphatidylcholine synthesis is elevated in neuronal models of Gaucher disease due to direct activation of CTP:phosphocholine cytidylyltransferase by glucosylceramide

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Recycling Compartments and the Internal Vesicles of Multivesicular Bodies Harbor Most of the Cholesterol Found in the Endocytic Pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

The N370S (Asn370-->Ser) mutation affects the capacity of glucosylceramidase to interact with anionic phospholipid-containing membranes and saposin C

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Selective effects of glucocerebroside (Gaucher's storage material) on macrophage cultures

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

The occurrence of psychosine and other glycolipids in spleen and liver from the three major types of Gaucher's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Sphingolipid hydrolases in brain tissue of patients with generalized gangliodosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

Jamming the endosomal system: lipid rafts and lysosomal storage diseases.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.08.001

10.1016/J.YMGME.2007.08.001

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17881272%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference