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M Cantz

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Biochemical and Biophysical Research Communications|June 5, 1970
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresisM Cantz, A Chrambach, E F Neufeld
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfataseJ F O'Brien, J Spranger, M Cantz
The Biochemical Journal|October 15, 1993
Protein catabolism in fibroblasts cultured from patients with mucolipidosis II and other lysosomal disordersJ Kopitz, A Arnold, T Meissner, et al.
European Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1994
[14C]Methylamine accumulation in cultured human skin fibroblasts--a biochemical test for lysosomal storage and lysosomal diseasesJ Kopitz, C Gerhard, P Höfler, et al.
Lancet (London, England)|November 4, 1978
Cardiac puncture of fetus with Hurler's disease avoiding abortion of unaffected co-twinA Aberg, F Mitelman, M Cantz, et al.
European Journal of Biochemistry|November 5, 1997
Partial characterization and enrichment of a membrane-bound sialidase specific for gangliosides from human brain tissueJ Kopitz, K Sinz, R Brossmer, et al.
Archives of Biochemistry and Biophysics|March 1, 1973
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblastsC W Hall, M Cantz, E F Neufeld
Biochemical and Biophysical Research Communications|May 15, 2001
The plasma membrane ganglioside sialidase cofractionates with markers of lipid raftsD Kalka, C von Reitzenstein, J Kopitz, et al.
European Journal of Biochemistry|February 1, 1982
Impaired phosphorylation of lysosomal enzymes in fibroblasts of patients with mucolipidosis IIIA Hasilik, A Waheed, M Cantz, et al.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
Biochemical and Biophysical Research Communications|June 5, 1970
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresisM Cantz, A Chrambach, E F Neufeld
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfataseJ F O'Brien, J Spranger, M Cantz
The Biochemical Journal|October 15, 1993
Protein catabolism in fibroblasts cultured from patients with mucolipidosis II and other lysosomal disordersJ Kopitz, A Arnold, T Meissner, et al.
European Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1994
[14C]Methylamine accumulation in cultured human skin fibroblasts--a biochemical test for lysosomal storage and lysosomal diseasesJ Kopitz, C Gerhard, P Höfler, et al.
Lancet (London, England)|November 4, 1978
Cardiac puncture of fetus with Hurler's disease avoiding abortion of unaffected co-twinA Aberg, F Mitelman, M Cantz, et al.
European Journal of Biochemistry|November 5, 1997
Partial characterization and enrichment of a membrane-bound sialidase specific for gangliosides from human brain tissueJ Kopitz, K Sinz, R Brossmer, et al.
Archives of Biochemistry and Biophysics|March 1, 1973
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblastsC W Hall, M Cantz, E F Neufeld
Biochemical and Biophysical Research Communications|May 15, 2001
The plasma membrane ganglioside sialidase cofractionates with markers of lipid raftsD Kalka, C von Reitzenstein, J Kopitz, et al.
European Journal of Biochemistry|February 1, 1982
Impaired phosphorylation of lysosomal enzymes in fibroblasts of patients with mucolipidosis IIIA Hasilik, A Waheed, M Cantz, et al.
Pageof 8