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Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|February 1, 1982
Phosphorylation of lysosomal enzymes in fibroblasts. Marked deficiency of N-acetylglucosamine-1-phosphotransferase in fibroblasts of patients with mucolipidosis IIIA Waheed, A Hasilik, M Cantz, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1973
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfataseG Bach, F Eisenberg, M Cantz, et al.European Journal of Cell Biology|May 1, 1997
Effects of cell surface ganglioside sialidase inhibition on growth control and differentiation of human neuroblastoma cellsJ Kopitz, C Mühl, V Ehemann, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristicsJ Gehler, A C Sewell, C Becker, et al.Helvetica Paediatrica Acta|January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian familyJ Gehler, A C Sewell, C Becker, et al.Pediatric Research|March 1, 1984
Partial deficiency of glycoprotein neuraminidase in some patients with Morquio disease type AJ Glössl, H Kresse, K Mendla, et al.The Biochemical Journal|May 15, 1989
Ganglioside GM3 sialidase activity in fibroblasts of normal individuals and of patients with sialidosis and mucolipidosis IV. Subcellular distribution and and some propertiesM Lieser, E Harms, H Kern, et al.Klinische Wochenschrift|August 17, 1981
The mucopolysaccharidoses: biochemistry and clinical symptomsH Kresse, M Cantz, K von Figura, et al.Padiatrie Und Padologie|January 1, 1983
[Chemotactic activity of fibroblasts in mucopolysaccharidoses]A Albini, B Pontz, H Mensing, et al.The Biochemical Journal|February 15, 1988
Defective lysosomal release of glycoprotein-derived sialic acid in fibroblasts from patients with sialic acid storage diseaseK Mendla, J Baumkötter, C Rosenau, et al.Pageof 7