GALACTOSIALIDOSIS

Known as: GSL, Lysosomal protective protein, deficiency of, Neuraminidase deficiency with beta-galactosidase deficiency 
 
National Institutes of Health

Papers overview

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2010
2010
Membrane lipids play a pivotal role in the pathogenesis of Alzheimer's disease, which is associated with conformational changes… (More)
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Highly Cited
2007
Highly Cited
2007
Understanding plant metabolism as an integrated system is essential for metabolic engineering aimed at the effective production… (More)
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Highly Cited
2007
Highly Cited
2007
Glycosphingolipids (GSLs) and their sialic acid-containing derivatives, gangliosides, are important cellular components and are… (More)
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Review
2005
Review
2005
Sphingosines, or sphingoids, are a family of naturally occurring long-chain hydrocarbon derivatives sharing a common 1,3… (More)
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Highly Cited
2004
Highly Cited
2004
Glycosphingolipids are endocytosed and targeted to the Golgi apparatus but are mistargeted to lysosomes in sphingolipid storage… (More)
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2004
2004
Three different mammalian sialidases have been described as follows: lysosomal (Neu1, gene NEU1), cytoplasmic (Neu2, gene NEU2… (More)
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Highly Cited
2001
Highly Cited
2001
Minimum cut/maximum flow algorithms on graphs have emerged as an increasingly useful tool for exactor approximate energy… (More)
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Review
2000
Review
2000
Glycosphingolipids (GSLs) and sphingomyelin in animal cells are clustered and organized as membrane microdomains closely… (More)
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Review
1995
Review
1995
Glycosphingolipids (GSLs), cell type-specific markers which change dramatically during ontogenesis and oncogenesis, have been… (More)
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1986
1986
The lysosomal storage disorder galactosialidosis has been recognized as a distinct genetic and biochemical entity, associated… (More)
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