Cell plasma membrane gangliosides content and pattern is finely regulated by a complex metabolic machinery. Among different pathways, past and new evidence suggests an important role of the sphingolipid catabolic enzymes associated with both lysosomes and plasma membrane. Over the years, several cell-free and cell-based assays are developed in order to evaluate the activities both intracellularly and at the cell surface. Here, we propose a selection of the most efficient, sensitive, and specific assays that allow determining the activity of the main gangliosides-glycohydrolases such as sialidases, f-hexosaminidases, f-galactosidases, and f-glucosidases in both cell/tissue lysates and directly in living cells
GM1 ganglioside carrying a fluorescent fatty acid in substitution of the natural one, has been admin...
AbstractGM1 ganglioside carrying a fluorescent fatty acid in substitution of the natural one, has be...
AbstractGM1-gangliosidosis is an inherited autosomal recessive disorder caused by mutations in the g...
'To whom correspondence should be addressed •Dedicated to Professor Glinter Quadbeck on the occ...
AbstractHuman fibroblasts produce ceramide from sialyllactosylceramide on the plasma membranes. Sial...
A lysosomal preparation, obtained from brain homogenate of 17-day-old C57BL mice by centrifugation o...
We describe herein the enzyme behavior of MmNEU3, the plasma membrane-associated sialidase from mous...
Human fibroblasts produce ceramide from sialyllactosylceramide on the plasma membranes. Sialidase Ne...
Gangliosides are a large group of complex lipids found predominantly on the outer layer of the plasm...
AbstractRat liver plasma membrane removed sialic acid from mixed bovine brain gangliosides more effi...
Qualitative and quantitative changes in glycosphingolipids, together with changes in the expression ...
<div><p>A new assay for the determination of lactosylceramide-2,3-sialyltransferase (SAT I, EC 2.4.9...
A new assay for the determination of lactosylceramide-2,3-sialyltransferase (SAT I, EC 2.4.99.9) and...
A new assay for the determination of lactosylceramide-2,3-sialyltransferase (SAT I, EC 2.4.99.9) and...
AbstractThe orientation of the catalytic site of a ganglioside-specific sialidase in the plasma memb...
GM1 ganglioside carrying a fluorescent fatty acid in substitution of the natural one, has been admin...
AbstractGM1 ganglioside carrying a fluorescent fatty acid in substitution of the natural one, has be...
AbstractGM1-gangliosidosis is an inherited autosomal recessive disorder caused by mutations in the g...
'To whom correspondence should be addressed •Dedicated to Professor Glinter Quadbeck on the occ...
AbstractHuman fibroblasts produce ceramide from sialyllactosylceramide on the plasma membranes. Sial...
A lysosomal preparation, obtained from brain homogenate of 17-day-old C57BL mice by centrifugation o...
We describe herein the enzyme behavior of MmNEU3, the plasma membrane-associated sialidase from mous...
Human fibroblasts produce ceramide from sialyllactosylceramide on the plasma membranes. Sialidase Ne...
Gangliosides are a large group of complex lipids found predominantly on the outer layer of the plasm...
AbstractRat liver plasma membrane removed sialic acid from mixed bovine brain gangliosides more effi...
Qualitative and quantitative changes in glycosphingolipids, together with changes in the expression ...
<div><p>A new assay for the determination of lactosylceramide-2,3-sialyltransferase (SAT I, EC 2.4.9...
A new assay for the determination of lactosylceramide-2,3-sialyltransferase (SAT I, EC 2.4.99.9) and...
A new assay for the determination of lactosylceramide-2,3-sialyltransferase (SAT I, EC 2.4.99.9) and...
AbstractThe orientation of the catalytic site of a ganglioside-specific sialidase in the plasma memb...
GM1 ganglioside carrying a fluorescent fatty acid in substitution of the natural one, has been admin...
AbstractGM1 ganglioside carrying a fluorescent fatty acid in substitution of the natural one, has be...
AbstractGM1-gangliosidosis is an inherited autosomal recessive disorder caused by mutations in the g...