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Journal of Inherited Metabolic Disease|July 10, 1999
Intracellular degradation of fluorescent glycolipids by lysosomal enzymes and their activatorsL Madar-Shapiro, M Pasmanik-Chor, T Dinur, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 29, 1996
Intracellular degradation of sulforhodamine-GM1: use for a fluorescence-based characterization of GM2-gangliosidosis variants in fibroblasts and white blood cellsV Agmon, R Khosravi, S Marchesini, et al.
Progress in Clinical and Biological Research|January 1, 1982
Gaucher disease: a membranous enzymopathyR J Desnick, G A Grabowski, T Dinur, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Human acid beta-glucosidase: isolation and amino acid sequence of a peptide containing the catalytic siteT Dinur, K M Osiecki, G Legler, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1992
Retroviral-mediated transfer of the human acid sphingomyelinase cDNA: correction of the metabolic defect in cultured Niemann-Pick disease cellsM Suchi, T Dinur, R J Desnick, et al.
The Journal of Biological Chemistry|June 25, 1986
Human acid beta-glucosidase. Use of conduritol B epoxide derivatives to investigate the catalytically active normal and Gaucher disease enzymesG A Grabowski, K Osiecki-Newman, T Dinur, et al.
The Biochemical Journal|January 23, 1999
Importance of splicing for prosaposin sortingL Madar-Shapiro, M Pasmanik-Chor, A M Vaccaro, et al.
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