Studies on sphingomyelinase and β-glucosidase activities in Niemann-Pick disease variants
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry,Biophysics
Reference33 articles.
1. The Metabolism of Sphingomyelin
2. The lysosomal localization of sphingolipid hydrolases
3. Magnesium-dependent sphingomyelinase
4. Sphingomyelinase in normal human spleens and in spleens from subjects with Niemann-Pick disease
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1. Cholesterol-dependent increases in glucosylceramide synthase activity in Niemann-Pick disease type C model cells: Abnormal trafficking of endogenously formed ceramide metabolites by inhibition of the enzyme;Neuropharmacology;2016-11
2. Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders;Molecular Genetics and Metabolism;2016-02
3. Gpnmb Is a Potential Marker for the Visceral Pathology in Niemann-Pick Type C Disease;PLOS ONE;2016-01-15
4. Effect of U18666a on Beta-Glucosidase, Sphingomyelinase, and Beta-Galactosidase Activities in Astrocytes of Young Rats;The Journal of Membrane Biology;2015-02-17
5. Regulation of Sterol Transport between Membranes and NPC2;Biochemistry;2008-09-30
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