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FEBS Letters|June 6, 1994
Intracellular trafficking of glycosphingolipids: role of sphingolipid activator proteins in the topology of endocytosis and lysosomal digestionK Sandhoff, A KleinClinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1977
A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and BH Christomanou, K SandhoffFEBS Letters|August 28, 1989
Identity of GD1C, GT1a and GQ1b synthase in Golgi vesicles from rat liverH Iber, K SandhoffHoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|December 1, 1979
Purification and characterization of an activator protein for the degradation of glycolipids GM2 and GA2 by hexosaminidase AE Conzelmann, K SandhoffDevelopmental Neuroscience|January 1, 1983
Partial enzyme deficiencies: residual activities and the development of neurological disordersE Conzelmann, K SandhoffDie Naturwissenschaften|March 1, 1988
[Sphingolipid storage diseases of the central nervous system: bases of biochemical and clinical heterogeneity]K Sandhoff, L QuinternProceedings of the National Academy of Sciences of the United States of America|August 1, 1978
AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2E Conzelmann, K SandhoffAdvances in Experimental Medicine and Biology|January 1, 1980
The specificity of human N-acetyl-beta-D-hexosaminidases towards glycosphincolipids is determined by an activator proteinE Conzelmann, K SandhoffArchiv Fur Psychiatrie Und Nervenkrankheiten|April 30, 1976
[Sphingolipid storage disease as an example of a molecular neuropathology (author's transl)]H Jatzkewitz, K SandhoffPageof 22