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GALACTOSIALIDOSIS

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

Related topics

Related topics

3 relations
CTSA genecongenital deficiency

Broader (1)

Lysosomal Storage Diseases

Papers overview

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2011
2011
Towards a selected reaction monitoring mass spectrometry fingerprint approach for the screening of oligosaccharidoses.
2011
2011
Localization behavior of Dirac particles in disordered graphene superlattices
Graphene superlattices (GSLs), formed by subjecting a monolayer graphene sheet to a periodic potential, can be used to engineer… 
2010
2010
Annulated diketopiperazines from dipeptides or Schöllkopf reagents via tandem cyclization-intramolecular N-arylation.
Facile CuI-mediated N-arylation of diketopiperazine using the Fukuyama modification of the Ullmann-Goldberg reaction can be… 
Highly Cited
2000
Highly Cited
2000
Endothelin‐1 in the brain of patients with galactosialidosis: Its abnormal increase and distribution pattern
Endothelin‐1 is a peptidic substrate in vitro of lysosomal protective protein/cathepsin A (PPCA) with serine carboxypeptidase… 
Highly Cited
1999
Highly Cited
1999
Evidence of LMP1–TRAF3 interactions in glycosphingolipid‐rich complexes of lymphoblastoid and nasopharyngeal carcinoma cells
Latent membrane protein 1 (LMP1) is an Epstein‐Barr virus (EBV) protein expressed in EBV‐transformed B lymphocytes and in… 
Highly Cited
1998
Highly Cited
1998
The neutral glycosphingolipid globotriaosylceramide promotes fusion mediated by a CD4-dependent CXCR4-utilizing HIV type 1 envelope glycoprotein.
Previously, we showed that the addition of human erythrocyte glycosphingolipids (GSLs) to nonhuman CD4(+) or GSL-depleted human… 
1995
1995
The Spatio-temporal Control of the Expression of Glutamine Synthetase in the Liver Is Mediated by Its 5′-Enhancer (*)
In previous studies of the glutamine synthetase gene, the promoter and two enhancer elements, one in the upstream region and one… 
1990
1990
A method for the rapid detection of urinary glycopeptides in alpha-N-acetylgalactosaminidase deficiency and other lysosomal storage diseases.
1985
1985
Galactosialidosis: A Comparative Study of Clinical and Biochemical Data on 22 Patients
AbstractTwenty-two patients with galactosialidosis were studied from clinical, biochemical, and genetic standpoints. A wide… 
1983
1983
Neutral glycosphingolipids of murine myeloma cells and helper, cytolytic, and suppressor T lymphocytes.
Functionally defined clones and lines of murine lymphocytes including myelomas, helper, suppressor and cytolytic T lymphocytes… 
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