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K Sandhoff

Showing results (161-170 of 256) with videos related to

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European Journal of Biochemistry|June 3, 1985
Incorporation and metabolism of ganglioside GM2 in skin fibroblasts from normal and GM2 gangliosidosis subjectsS Sonderfeld, E Conzelmann, G Schwarzmann, et al.
Haematology and Blood Transfusion|January 1, 1987
Hexosaminidase I indicates maturation disarrangement in acute leukemiasJ R Novotny, S Brendler, H J Kytzia, et al.
Human Genetics|November 1, 1993
Molecular genetics of GM2-gangliosidosis AB variant: a novel mutation and expression in BHK cellsM Schröder, D Schnabel, R Hurwitz, et al.
Biochemical and Biophysical Research Communications|May 16, 1994
Sphingolipid activator protein D (sap-D) stimulates the lysosomal degradation of ceramide in vivoA Klein, M Henseler, C Klein, et al.
FEBS Letters|December 16, 1996
Purification of acid sphingomyelinase from human placenta: characterization and N-terminal sequenceS Lansmann, K Ferlinz, R Hurwitz, et al.
Journal of Biotechnology|October 9, 1998
Expression of recombinant human acid sphingomyelinase in insect Sf21 cells: purification, processing and enzymatic characterizationO Bartelsen, S Lansmann, M Nettersheim, et al.
The Journal of Biological Chemistry|February 14, 1998
1-Methylthiodihydroceramide, a novel analog of dihydroceramide, stimulates sphinganine degradation resulting in decreased de novo sphingolipid biosynthesisG van Echten-Deckert, A Giannis, A Schwarz, et al.
European Journal of Biochemistry|January 15, 1997
Functional characterization of the N-glycosylation sites of human acid sphingomyelinase by site-directed mutagenesisK Ferlinz, R Hurwitz, H Moczall, et al.
Glycoconjugate Journal|April 1, 1996
The effect of fumonisin B1 on developing chick embryos: correlation between de novo sphingolipid biosynthesis and gross morphological changesC Zacharias, G van Echten-Deckert, E Wang, et al.
American Journal of Human Genetics|January 1, 1996
Analysis of a splice-site mutation in the sap-precursor gene of a patient with metachromatic leukodystrophyM Henseler, A Klein, M Reber, et al.
Pageof 26

Showing results (161-170 of 256) with videos related to

Sort By:
Pageof 26
European Journal of Biochemistry|June 3, 1985
Incorporation and metabolism of ganglioside GM2 in skin fibroblasts from normal and GM2 gangliosidosis subjectsS Sonderfeld, E Conzelmann, G Schwarzmann, et al.
Haematology and Blood Transfusion|January 1, 1987
Hexosaminidase I indicates maturation disarrangement in acute leukemiasJ R Novotny, S Brendler, H J Kytzia, et al.
Human Genetics|November 1, 1993
Molecular genetics of GM2-gangliosidosis AB variant: a novel mutation and expression in BHK cellsM Schröder, D Schnabel, R Hurwitz, et al.
Biochemical and Biophysical Research Communications|May 16, 1994
Sphingolipid activator protein D (sap-D) stimulates the lysosomal degradation of ceramide in vivoA Klein, M Henseler, C Klein, et al.
FEBS Letters|December 16, 1996
Purification of acid sphingomyelinase from human placenta: characterization and N-terminal sequenceS Lansmann, K Ferlinz, R Hurwitz, et al.
Journal of Biotechnology|October 9, 1998
Expression of recombinant human acid sphingomyelinase in insect Sf21 cells: purification, processing and enzymatic characterizationO Bartelsen, S Lansmann, M Nettersheim, et al.
The Journal of Biological Chemistry|February 14, 1998
1-Methylthiodihydroceramide, a novel analog of dihydroceramide, stimulates sphinganine degradation resulting in decreased de novo sphingolipid biosynthesisG van Echten-Deckert, A Giannis, A Schwarz, et al.
European Journal of Biochemistry|January 15, 1997
Functional characterization of the N-glycosylation sites of human acid sphingomyelinase by site-directed mutagenesisK Ferlinz, R Hurwitz, H Moczall, et al.
Glycoconjugate Journal|April 1, 1996
The effect of fumonisin B1 on developing chick embryos: correlation between de novo sphingolipid biosynthesis and gross morphological changesC Zacharias, G van Echten-Deckert, E Wang, et al.
American Journal of Human Genetics|January 1, 1996
Analysis of a splice-site mutation in the sap-precursor gene of a patient with metachromatic leukodystrophyM Henseler, A Klein, M Reber, et al.
Pageof 26