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A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity
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Saposin C is required for lipid presentation by human CD1b
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LC3 conjugation system in mammalian autophagy
I Tanida et al.
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Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse
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Saposin C is required for normal resistance of acid β-glucosidase to proteolytic degradation
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A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation
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LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing
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Further studies on the reconstitution of glucosylceramidase activity by Sap C and anionic phospholipids
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