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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1982
Molecular defect in combined beta-galactosidase and neuraminidase deficiency in manA D'Azzo, A Hoogeveen, A J Reuser, et al.Genes & Development|December 15, 1996
Characterization of human lysosomal neuraminidase defines the molecular basis of the metabolic storage disorder sialidosisE Bonten, A van der Spoel, M Fornerod, et al.Journal of Lipid Research|February 3, 2005
Substrate reduction reduces gangliosides in postnatal cerebrum-brainstem and cerebellum in GM1 gangliosidosis miceJ L Kasperzyk, A d'Azzo, F M Platt, et al.Human Genetics|November 1, 1988
The presence of a reduced amount of 32-kd "protective" protein is a distinct biochemical finding in late infantile galactosialidosisP Strisciuglio, G Parenti, C Giudice, et al.Clinical Genetics|November 1, 1984
Non-progressive psychomotor retardation in a child with severe deficiency of arylsulphatase A activityC Danesino, A D'Azzo, M Aricò, et al.The Journal of Biological Chemistry|August 5, 1991
Human lysosomal protective protein has cathepsin A-like activity distinct from its protective functionN J Galjart, H Morreau, R Willemsen, et al.The EMBO Journal|December 1, 1991
A mutation in a mild form of galactosialidosis impairs dimerization of the protective protein and renders it unstableX Y Zhou, N J Galjart, R Willemsen, et al.The Journal of Biological Chemistry|November 3, 1995
Lysosomal protective protein/cathepsin A. Role of the "linker" domain in catalytic activationE J Bonten, N J Galjart, R Willemsen, et al.The Journal of Biological Chemistry|September 5, 1992
Human lysosomal protective protein. Glycosylation, intracellular transport, and association with beta-galactosidase in the endoplasmic reticulumH Morreau, N J Galjart, R Willemsen, et al.The Journal of Biological Chemistry|September 10, 1984
Faulty association of alpha- and beta-subunits in some forms of beta-hexosaminidase A deficiencyA d'Azzo, R L Proia, E H Kolodny, et al.Pageof 6