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K Sandhoff

Showing results (181-190 of 256) with videos related to

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The Biochemical Journal|June 1, 1993
Over-expression of a functionally active human GM2-activator protein in Escherichia coliH Klima, A Klein, G van Echten, et al.
The Journal of Biological Chemistry|April 25, 1991
Sulfatide activator protein. Alternative splicing that generates three mRNAs and a newly found mutation responsible for a clinical diseaseH Holtschmidt, K Sandhoff, H Y Kwon, et al.
Journal of Inherited Metabolic Disease|February 22, 2000
A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD)D Wrobe, M Henseler, S Huettler, et al.
European Journal of Biochemistry|December 1, 1992
Ganglioside binding proteins of calf brain with ubiquitin-like N-terminalsE Zdebska, J Antoniewicz, B Nilsson, et al.
FEBS Letters|September 9, 1991
Characterization of full-length cDNAs and the gene coding for the human GM2 activator proteinH Klima, A Tanaka, D Schnabel, et al.
FEBS Letters|January 15, 1979
Sialidase deficiency in adult-type neuronal storage diseaseT Miyatake, T Yamada, M Suzuki, et al.
Biological Chemistry|April 20, 2001
Stimulation of acid sphingomyelinase activity by lysosomal lipids and sphingolipid activator proteinsT Linke, G Wilkening, S Lansmann, et al.
The Journal of Biological Chemistry|December 6, 2000
Interfacial regulation of acid ceramidase activity. Stimulation of ceramide degradation by lysosomal lipids and sphingolipid activator proteinsT Linke, G Wilkening, F Sadeghlar, et al.
Journal of Lipid Research|February 11, 1998
Turnover of endogenous ceramide in cultured normal and Farber fibroblastsG van Echten-Deckert, A Klein, T Linke, et al.
American Journal of Human Genetics|January 1, 1985
Hereditary heat-labile hexosaminidase B: a variant whose homozygotes synthesize a functional HEX AR Navon, R Kopel, J Nutman, et al.
Pageof 26

Showing results (181-190 of 256) with videos related to

Sort By:
Pageof 26
The Biochemical Journal|June 1, 1993
Over-expression of a functionally active human GM2-activator protein in Escherichia coliH Klima, A Klein, G van Echten, et al.
The Journal of Biological Chemistry|April 25, 1991
Sulfatide activator protein. Alternative splicing that generates three mRNAs and a newly found mutation responsible for a clinical diseaseH Holtschmidt, K Sandhoff, H Y Kwon, et al.
Journal of Inherited Metabolic Disease|February 22, 2000
A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD)D Wrobe, M Henseler, S Huettler, et al.
European Journal of Biochemistry|December 1, 1992
Ganglioside binding proteins of calf brain with ubiquitin-like N-terminalsE Zdebska, J Antoniewicz, B Nilsson, et al.
FEBS Letters|September 9, 1991
Characterization of full-length cDNAs and the gene coding for the human GM2 activator proteinH Klima, A Tanaka, D Schnabel, et al.
FEBS Letters|January 15, 1979
Sialidase deficiency in adult-type neuronal storage diseaseT Miyatake, T Yamada, M Suzuki, et al.
Biological Chemistry|April 20, 2001
Stimulation of acid sphingomyelinase activity by lysosomal lipids and sphingolipid activator proteinsT Linke, G Wilkening, S Lansmann, et al.
The Journal of Biological Chemistry|December 6, 2000
Interfacial regulation of acid ceramidase activity. Stimulation of ceramide degradation by lysosomal lipids and sphingolipid activator proteinsT Linke, G Wilkening, F Sadeghlar, et al.
Journal of Lipid Research|February 11, 1998
Turnover of endogenous ceramide in cultured normal and Farber fibroblastsG van Echten-Deckert, A Klein, T Linke, et al.
American Journal of Human Genetics|January 1, 1985
Hereditary heat-labile hexosaminidase B: a variant whose homozygotes synthesize a functional HEX AR Navon, R Kopel, J Nutman, et al.
Pageof 26