Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/93578
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Type: Journal article
Title: Gaucher's disease in the lipidomics era
Author: Fuller, M.
Citation: Clinical Lipidology, 2012; 7(4):431-441
Publisher: Future Medicine
Issue Date: 2012
ISSN: 1758-4299
1758-4302
Statement of
Responsibility: 
Maria Fuller
Abstract: Human diseases that result directly from alterations in sphingolipid metabolism are generally disorders of the degradation of these compounds. A defect in the lysosomal degradation of glucosylceramide results in the phenotype of Gaucher’s disease, the most common of the sphingolipidoses. The majority of cases of Gaucher’s disease result from mutations in the gene encoding the lysosomal enzyme, acid β-glucosidase. Although generally regarded as a single-gene disorder, in reality the disorder is complex, multifactorial and progressive. Understanding the pathogenic cascade in Gaucher’s disease will require an integrated and convincing biological approach; this review aims to explore how the study of sphingolipids, in addition to glucosylceramide, phospholipids and other related lipids, are advancing us towards achieving this goal.
Keywords: Gaucher’s disease; glucosylceramide; lipid rafts; lysosome; mass spectrometry; phospholipid; sphingolipid
Rights: Copyright status unknown
RMID: 0030032127
DOI: 10.2217/CLP.12.39
Appears in Collections:Medicine publications

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