Secondary sphingolipid accumulation in a macrophage model of Gaucher disease. (Q55044639)

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7 January 2020

title

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

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7 January 2020

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2

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John J Hopwood

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7 January 2020

author name string

Leanne K Hein

series ordinal

1

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Maria Fuller

series ordinal

4

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publication date

18 September 2007

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Molecular Genetics and Metabolism

7 January 2020

published in

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volume

92

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issue

4

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page(s)

336-345

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

7 January 2020

cites work

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7 January 2021

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

7 January 2021

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The pathogenesis of glycosphingolipid storage disorders

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Glucosylceramide modulates membrane traffic along the endocytic pathway

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

7 January 2021

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Glycosphingolipids are required for sorting melanosomal proteins in the Golgi complex

7 January 2021

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

7 January 2021

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

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

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

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

7 January 2021

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Regulation of ceramide production and apoptosis

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Sphingolipid hydrolases in brain tissue of patients with generalized gangliodosis

7 January 2021

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

7 January 2021

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10.1016/J.YMGME.2007.08.001

7 January 2021

Identifiers

DOI

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7 January 2020

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