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glycosphingolipid metabolic process

Known as: glycosphingolipid metabolism 
The chemical reactions and pathways involving glycosphingolipids, any compound with residues of sphingoid and at least one monosaccharide. [ISBN… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
No difference in glycosphingolipid metabolism and mitochondrial function in glucocorticoid-induced insulin resistance in healthy men.
OBJECTIVE Glucocorticoids (GCs) are well known to induce insulin resistance; however, mechanisms that cause the impairement of… 
Review
2012
Review
2012
Fabry International Prognostic Index: a predictive severity score for Anderson-Fabry disease
Background Anderson-Fabry disease (AFD) is a disorder of glycosphingolipid metabolism resulting from deficiency of… 
Review
2011
Review
2011
Sphingolipid metabolism and drug resistance in hematological malignancies.
Drug resistance represents a serious barrier to the successful treatment of hematological malignancies. In leukemias, resistance… 
2009
2009
Proteomic analysis of enriched lysosomes at early phase of camptothecin-induced apoptosis in human U-937 cells.
Review
1999
Review
1999
Recent advances in the biochemistry of glycosphingolipid metabolism.
1991
1991
Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an NcoI polymorphism detected by an alpha-galactosidase cDNA clone.
Fabry disease is an X linked recessive disorder of glycosphingolipid metabolism resulting from a deficiency of the lysosomal… 
1990
1990
Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosis
1988
1988
Cardiovascular Manifestations in Fabry's Disease — Age‐Related Changes in Hemizygotes and Heterozygotes —
Fabry's disease is an X‐linked recessive disorder of glycosphingolipid metabolism. Accumulation of neutral sphingolipid in… 
1983
1983
Amiodarone phenocopy of Fabry's keratopathy.
To the Editor.— Recognition of the distinctive corneal opacity associated with amiodarone therapy has stimulated our interest in… 
Highly Cited
1974
Highly Cited
1974
Ganglioside catabolism in hexosaminidase A-deficient adults
TAY-SACHS disease is an inborn error of glycosphingolipid metabolism characterised by the accumulation of N-acetyl-galactosaminyl… 
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