globotriaosyl lysosphingolipid

Known as: lyso-Gb3, Gb3 lysosphingolipid, lysoGb3 
 
National Institutes of Health

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2015
2015
BACKGROUND Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, has a heterogeneous… (More)
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2015
2015
Fabry disease is an X-linked lysosomal storage disorder characterised by accumulation of glycosphingolipids, and accompanied by… (More)
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2013
2013
BACKGROUND Biochemical markers that accurately reflect the severity and progression of disease in patients with Fabry disease and… (More)
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2013
2013
BACKGROUND Previous studies revealed a high incidence of late-onset Fabry disease mutation, IVS4+919G>A, in Taiwan. However, the… (More)
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Highly Cited
2012
Highly Cited
2012
Staphylococci cause bovine mastitis, with Staphylococcus aureus being responsible for the majority of the mastitis-based losses… (More)
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2012
2012
INTRODUCTION Enzyme replacement therapy (ERT) with alpha-Galactosidase A (aGal A) may cause antibody (AB) formation against aGal… (More)
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Highly Cited
2011
Highly Cited
2011
Fabry disease is treated by two-weekly infusions with α-galactosidase A, which is deficient in this X-linked… (More)
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Highly Cited
2010
Highly Cited
2010
Fabry disease is an X-linked lysosomal storage disorder due to deficiency of alpha-Galactosidase A, causing accumulation of… (More)
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2009
2009
Verotoxin binding to its receptor, globotriaosyl ceramide(Gb(3)) mediates the glomerular pathology of hemolytic uremic syndrome… (More)
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1994
1994
The glycosphingolipid globotriaosyl ceramide (CD77) and other globo-series glycolipids containing terminal galactose (Gal)alpha 1… (More)
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