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K Sandhoff

Showing results (21-30 of 256) with videos related to

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Neuropediatrics|September 1, 1984
The biochemical basis of gangliosidosesK Sandhoff, E Conzelmann
Die Naturwissenschaften|March 1, 1988
[Sphingolipid storage diseases of the central nervous system: bases of biochemical and clinical heterogeneity]K Sandhoff, L Quintern
Biochemistry|December 11, 1990
Metabolism and intracellular transport of glycosphingolipidsG Schwarzmann, K Sandhoff
Journal of Inherited Metabolic Disease|September 5, 1998
Glycosphingolipid degradation and animal models of GM2-gangliosidosesT Kolter, K Sandhoff
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|August 1, 1971
[Enrichment and characterization of 2 forms of human N-acetyl-beta-D-hexosaminidase]K Sandhoff, W Wässle
Acta Biochimica Polonica|November 20, 1998
Processing of sphingolipid activator proteins and the topology of lysosomal digestionK Sandhoff, T Kolter
Proceedings 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 Sandhoff
Methods of Biochemical Analysis|January 1, 1987
Activator proteins for lysosomal glycolipid hydrolysisE Conzelmann, K Sandhoff
Methods in Enzymology|January 1, 1987
Activator proteins for lysosomal glycolipid hydrolysisE Conzelmann, K Sandhoff
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 22, 1998
Biochemistry of glycosphingolipid degradationK Sandhoff, T Kolter
Pageof 26

Showing results (21-30 of 256) with videos related to

Sort By:
Pageof 26
Neuropediatrics|September 1, 1984
The biochemical basis of gangliosidosesK Sandhoff, E Conzelmann
Die Naturwissenschaften|March 1, 1988
[Sphingolipid storage diseases of the central nervous system: bases of biochemical and clinical heterogeneity]K Sandhoff, L Quintern
Biochemistry|December 11, 1990
Metabolism and intracellular transport of glycosphingolipidsG Schwarzmann, K Sandhoff
Journal of Inherited Metabolic Disease|September 5, 1998
Glycosphingolipid degradation and animal models of GM2-gangliosidosesT Kolter, K Sandhoff
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|August 1, 1971
[Enrichment and characterization of 2 forms of human N-acetyl-beta-D-hexosaminidase]K Sandhoff, W Wässle
Acta Biochimica Polonica|November 20, 1998
Processing of sphingolipid activator proteins and the topology of lysosomal digestionK Sandhoff, T Kolter
Proceedings 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 Sandhoff
Methods of Biochemical Analysis|January 1, 1987
Activator proteins for lysosomal glycolipid hydrolysisE Conzelmann, K Sandhoff
Methods in Enzymology|January 1, 1987
Activator proteins for lysosomal glycolipid hydrolysisE Conzelmann, K Sandhoff
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 22, 1998
Biochemistry of glycosphingolipid degradationK Sandhoff, T Kolter
Pageof 26