22 results on '"Sandhoff, K."'
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2. Correlation between enzyme activity and substrate storage in a cell culture model system for Gaucher disease
3. Restoration of the GM2 Ganglioside Metabolism in Bone Marrow–Derived Stromal Cells from Tay-Sachs Disease Animal Model
4. Uptake of Mannose-Terminal Glucocerebrosidase in Cultured Human Cholinergic and Dopaminergic Neuron Cell Lines
5. A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD)
6. Gangliosides are Transported from the Plasma Membrane to Intralysosomal Membranes as Revealed by Immuno-Electron Microscopy
7. Glycosphingolipid degradation and animal models of GM2-gangliosidoses
8. Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disorders
9. Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease
10. S7.1 Topology and regulation of glycolipid metabolism
11. Glycolipids of the cell surface: Biosynthesis and topology of metabolism
12. Genetic complementation in somatic cell hybrids of four variants of infantile GM2 gangliosidosis
13. Substrate specificities of a bacterial sialidase and rat liver ganglioside GM3 sialyltransferase
14. Diagnosis of infantile and juvenile forms of GM2 gangliosidosis variant 0. residual activities toward natural and different synthetic substrates
15. The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patients
16. Biochemistry and Genetics of gangliosidoses
17. Wolman's disease: Clinical, biochemical and ultrastructural studies in an unusual case without striking adrenal calcification
18. Juvenile GM2-Gangliosidose mit veränderter Substratspezifität der Hexosaminidase A
19. Die infantile amaurotische Idiotie und verwandte Formen als Gangliosid-Speicherkrankheiten
20. Prenatal diagnosis of tay-sachs disease in cell-free amniotic fluid
21. Enzymatische Untersuchungen im Blut von Überträgern einer Variante der Tay-Sachsschen Erkrankung (Variate O)
22. Biochemistry and genetics of gangliosidoses
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