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M Cantz

Showing results (31-40 of 72) with videos related to

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Biochemical and Biophysical Research Communications|March 30, 1994
Role of plasma membrane ganglioside sialidase of human neuroblastoma cells in growth control and differentiationJ Kopitz, C von Reitzenstein, C Mühl, et al.
Glycobiology|April 1, 1996
Selective ganglioside desialylation in the plasma membrane of human neuroblastoma cellsJ Kopitz, C von Reitzenstein, K Sinz, et al.
The Journal of Biological Chemistry|September 10, 1972
The Hunter corrective factor. Purification and preliminary characterizationM Cantz, A Chrambach, G Bach, et al.
European Journal of Biochemistry|February 13, 2001
Differential functional relevance of a plasma membrane ganglioside sialidase in cholinergic and adrenergic neuroblastoma cell linesC von Reitzenstein, J Kopitz, V Schuhmann, et al.
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.
Lancet (London, England)|November 2, 1974
Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiencyJ Spranger, J Gehler, J F O'Brien, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1978
Increased urinary excretion of keratan sulfate in fucosidosisH Greiling, H W Stuhlsatz, 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.
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.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
Biochemical and Biophysical Research Communications|March 30, 1994
Role of plasma membrane ganglioside sialidase of human neuroblastoma cells in growth control and differentiationJ Kopitz, C von Reitzenstein, C Mühl, et al.
Glycobiology|April 1, 1996
Selective ganglioside desialylation in the plasma membrane of human neuroblastoma cellsJ Kopitz, C von Reitzenstein, K Sinz, et al.
The Journal of Biological Chemistry|September 10, 1972
The Hunter corrective factor. Purification and preliminary characterizationM Cantz, A Chrambach, G Bach, et al.
European Journal of Biochemistry|February 13, 2001
Differential functional relevance of a plasma membrane ganglioside sialidase in cholinergic and adrenergic neuroblastoma cell linesC von Reitzenstein, J Kopitz, V Schuhmann, et al.
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.
Lancet (London, England)|November 2, 1974
Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiencyJ Spranger, J Gehler, J F O'Brien, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1978
Increased urinary excretion of keratan sulfate in fucosidosisH Greiling, H W Stuhlsatz, 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.
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.
Pageof 8