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K Sandhoff

Showing results (251-260 of 256) with videos related to

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Genomics|December 28, 1999
The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expressionC M Li, J H Park, X He, et al.
The Journal of Biological Chemistry|March 14, 2000
Purification and characterization of a magnesium-dependent neutral sphingomyelinase from bovine brainK Bernardo, O Krut, K Wiegmann, et al.
The Journal of Biological Chemistry|January 3, 2001
Mice expressing only monosialoganglioside GM3 exhibit lethal audiogenic seizuresH Kawai, M L Allende, R Wada, et al.
Human Molecular Genetics|June 18, 2005
A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay-Sachs diseaseS Martino, P Marconi, B Tancini, et al.
Nature Genetics|November 1, 1996
Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosisK Sango, M P McDonald, J N Crawley, et al.
The Journal of Clinical Investigation|February 18, 1999
A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorderY Liu, R Wada, H Kawai, et al.
Pageof 26

Showing results (251-260 of 256) with videos related to

Sort By:
Pageof 26
You have reached the last page of results.This site can display upto 256 results.
Genomics|December 28, 1999
The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expressionC M Li, J H Park, X He, et al.
The Journal of Biological Chemistry|March 14, 2000
Purification and characterization of a magnesium-dependent neutral sphingomyelinase from bovine brainK Bernardo, O Krut, K Wiegmann, et al.
The Journal of Biological Chemistry|January 3, 2001
Mice expressing only monosialoganglioside GM3 exhibit lethal audiogenic seizuresH Kawai, M L Allende, R Wada, et al.
Human Molecular Genetics|June 18, 2005
A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay-Sachs diseaseS Martino, P Marconi, B Tancini, et al.
Nature Genetics|November 1, 1996
Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosisK Sango, M P McDonald, J N Crawley, et al.
The Journal of Clinical Investigation|February 18, 1999
A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorderY Liu, R Wada, H Kawai, et al.
Pageof 26