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The Journal of Biological Chemistry|July 14, 2001
Human acid ceramidase: processing, glycosylation, and lysosomal targetingK Ferlinz, G Kopal, K Bernardo, et al.Genomics|December 28, 1999
Molecular cloning and characterization of a human cDNA and gene encoding a novel acid ceramidase-like proteinS B Hong, C M Li, H J Rhee, et al.Nature Genetics|July 1, 1995
Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick diseaseK Horinouchi, S Erlich, D P Perl, et al.Genomics|July 8, 1998
Cloning and characterization of the full-length cDNA and genomic sequences encoding murine acid ceramidaseC M Li, S B Hong, G Kopal, et al.The Journal of Experimental Medicine|January 7, 1998
Lipopolysaccharide induces disseminated endothelial apoptosis requiring ceramide generationA Haimovitz-Friedman, C Cordon-Cardo, S Bayoumy, et al.Cell|July 26, 1996
Acid sphingomyelinase-deficient human lymphoblasts and mice are defective in radiation-induced apoptosisP Santana, L A Peña, A Haimovitz-Friedman, et al.The Journal of Biological Chemistry|December 20, 1996
Molecular cloning and characterization of a full-length complementary DNA encoding human acid ceramidase. Identification Of the first molecular lesion causing Farber diseaseJ Koch, S Gärtner, C M Li, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
Restoration of normal lysosomal function in mucopolysaccharidosis type VII cells by retroviral vector-mediated gene transferJ H Wolfe, E H Schuchman, L E Stramm, et al.The Journal of Biological Chemistry|March 18, 2000
Role of acidic sphingomyelinase in Fas/CD95-mediated cell deathT Lin, L Genestier, M J Pinkoski, et al.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.Pageof 8