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ganglioside catabolic process

Known as: ganglioside breakdown, ganglioside catabolism, ganglioside degradation 
The chemical reactions and pathways resulting in the breakdown of ganglioside, a ceramide oligosaccharide carrying, in addition to other sugar… Expand
National Institutes of Health

Papers overview

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2015
2015
Tay–Sachs disease is a severe lysosomal storage disorder caused by mutations in the HEXA gene coding for α subunit of lysosomal… Expand
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2015
2015
Transient Receptor Potential (TRP) cation channels, such as TRP Vanilloid 1 and TRP Ankyrin repeat domain 1 (TRPV1 and TRPA1) are… Expand
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Review
2013
Review
2013
Gangliosides are the main glycolipids of neuronal plasma membranes. Their surface patterns are generated by coordinated processes… Expand
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2008
2008
Mammalian sialidase Neu4, ubiquitously expressed in human tissues, is located in the lysosomal and mitochondrial lumen and has… Expand
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Highly Cited
2007
Highly Cited
2007
Human plasma membrane-associated sialidase (NEU3), a key enzyme for ganglioside degradation, is markedly upregulated in human… Expand
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2006
2006
We have found previously that human plasma-membrane-associated sialidase (NEU3), a key glycosidase for ganglioside degradation… Expand
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2005
2005
The metabolic processing of GM1 ganglioside, exogenously administered to cultured skin fibroblasts, was investigated on cells… Expand
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Review
2004
Review
2004
Glycosphingolipids (GSLs) known as gangliosides have been documented to accumulate in a wide range of lysosomal storage disorders… Expand
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Highly Cited
1995
Highly Cited
1995
Tay–Sachs and Sandhoff diseases are clinically similar neurodegenerative disorders. These two sphingolipidoses are characterized… Expand
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1985
1985
Microsomal membranes isolated from calf brain contain a sialidase which cleaves ganglioside substrates naturally occurring within… Expand
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