E H Schuchman - JoVE Visualize

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Enzyme|January 1, 1984

Human alpha-L-iduronidase. II. Comparative biochemical and immunologic properties of the purified low and high uptake formsE H Schuchman, N A Guzman, G Takada, et al.

The Journal of Biological Chemistry|August 2, 1996

Zn2+-stimulated sphingomyelinase is secreted by many cell types and is a product of the acid sphingomyelinase geneS L Schissel, E H Schuchman, K J Williams, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984

Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.

Genomics|February 1, 1992

Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1)E H Schuchman, O Levran, L V Pereira, et al.

The Journal of Experimental Medicine|April 4, 1998

Acidic sphingomyelinase (ASM) is necessary for fas-induced GD3 ganglioside accumulation and efficient apoptosis of lymphoid cellsR De Maria, M R Rippo, E H Schuchman, et al.

American Journal of Human Genetics|April 1, 1992

Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneityW D Jin, C E Jackson, R J Desnick, et al.

Enzyme|January 1, 1989

Characterization of the defective beta-glucuronidase activity in canine mucopolysaccharidosis type VIIE H Schuchman, T K Toroyan, M E Haskins, et al.

The Journal of Biological Chemistry|May 5, 1991

Human acid sphingomyelinase. Isolation, nucleotide sequence and expression of the full-length and alternatively spliced cDNAsE H Schuchman, M Suchi, T Takahashi, et al.

The Journal of Biological Chemistry|June 25, 1992

Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic formsT Takahashi, M Suchi, R J Desnick, 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.

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Showing results (21-30 of 71) with videos related to

Sort By:

Pageof 8

Enzyme|January 1, 1984

Human alpha-L-iduronidase. II. Comparative biochemical and immunologic properties of the purified low and high uptake formsE H Schuchman, N A Guzman, G Takada, et al.

The Journal of Biological Chemistry|August 2, 1996

Zn2+-stimulated sphingomyelinase is secreted by many cell types and is a product of the acid sphingomyelinase geneS L Schissel, E H Schuchman, K J Williams, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984

Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.

Genomics|February 1, 1992

Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1)E H Schuchman, O Levran, L V Pereira, et al.

The Journal of Experimental Medicine|April 4, 1998

Acidic sphingomyelinase (ASM) is necessary for fas-induced GD3 ganglioside accumulation and efficient apoptosis of lymphoid cellsR De Maria, M R Rippo, E H Schuchman, et al.

American Journal of Human Genetics|April 1, 1992

Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneityW D Jin, C E Jackson, R J Desnick, et al.

Enzyme|January 1, 1989

Characterization of the defective beta-glucuronidase activity in canine mucopolysaccharidosis type VIIE H Schuchman, T K Toroyan, M E Haskins, et al.

The Journal of Biological Chemistry|May 5, 1991

Human acid sphingomyelinase. Isolation, nucleotide sequence and expression of the full-length and alternatively spliced cDNAsE H Schuchman, M Suchi, T Takahashi, et al.

The Journal of Biological Chemistry|June 25, 1992

Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic formsT Takahashi, M Suchi, R J Desnick, 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.

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