globotriaosylceramide

Known as: Ganglioside GA3, O-alpha-D-galactopyranosyl-(1-4B)-, Gal-1-4-Gal-1-4-Glc-cer, P(K) antigen 
 
National Institutes of Health

Papers overview

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2016
2016
Type VI secretion systems (T6SSs) are multiprotein complexes best studied in Gram-negative pathogens where they have been shown… (More)
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2010
2010
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency in alpha-galactosidase A (alpha-Gal A) activity… (More)
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2010
2010
Neurological damage caused by intoxication with Shiga toxin (Stx) from enterohemorrhagic Escherichia coli is the most… (More)
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Highly Cited
2008
Highly Cited
2008
Fabry disease is an X-linked lysosomal storage disease caused by deficiency of alpha-galactosidase A that affects males and shows… (More)
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2007
2007
The pathogenesis of Fabry disease is poorly understood. We used a variety of immunohistological techniques to localize… (More)
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2007
2007
In birds, ACTH release from the anterior pituitary gland during stress is controlled by CRH and arginine vasotocin (AVT). Using 5… (More)
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2002
2002
Resonances in the carbon-13 natural abundance, proton-decoupled, 90.5 MHz nuclear magnetic resonance spectrum of… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Fabry's disease, lysosomal alpha-galactosidase A deficiency, results from the progressive accumulation of… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Fabry disease is an X-linked lysosomal deficiency of alpha-galactosidase A that results in cellular accumulation of… (More)
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Highly Cited
2000
Highly Cited
2000
We used a potent inhibitor of glucosylceramide synthase to test whether substrate deprivation could lower globotriaosylceramide… (More)
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