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M van Sande

Showing results (41-50 of 55) with videos related to

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Biochimica Et Biophysica Acta|April 23, 1990
Purification and characterization of a new arginine carboxypeptidase in human serumD Hendriks, W Wang, S Scharpé, et al.
Monographs in Human Genetics|January 1, 1972
Congenital hypophosphatasia. Report on two cases with special reference to phosphoethanolamine excretionH G Terheggen, C Schildberg, W Schürer, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1970
[Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]H G Terheggen, A Schwenk, A Lowenthal, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Post synthetic modification of CK-MM by kininase IM van Sande, D Hendriks, J Soons, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1988
Identification of the carboxypeptidase responsible for the post-synthetic modification of creatine kinase in human serumD Hendriks, J Soons, S Scharpé, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1970
[Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]H G Terheggen, A Schwenk, A Lowenthal, et al.
Journal De Genetique Humaine|March 1, 1972
Familial hyperargininemiaH G Terheggen, F Lavinha, J P Colombo, et al.
Biochimie|January 1, 1991
Proteases and their inhibitors: today and tomorrowS Scharpe, I De Meester, D Hendriks, et al.
Biochemical Society Transactions|August 1, 1990
Dipeptidyl peptidase IV in human lymphocytes: molecular propertiesI de Meester, G Vanhoof, S Scharpé, et al.
Urologia Internationalis|January 1, 1985
Tripeptidyl carboxypeptidase activity of angiotensin-converting enzyme in human tissues of the urogenital tractM van Sande, J Inokuchi, A Nagamatsu, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Biochimica Et Biophysica Acta|April 23, 1990
Purification and characterization of a new arginine carboxypeptidase in human serumD Hendriks, W Wang, S Scharpé, et al.
Monographs in Human Genetics|January 1, 1972
Congenital hypophosphatasia. Report on two cases with special reference to phosphoethanolamine excretionH G Terheggen, C Schildberg, W Schürer, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1970
[Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]H G Terheggen, A Schwenk, A Lowenthal, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Post synthetic modification of CK-MM by kininase IM van Sande, D Hendriks, J Soons, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1988
Identification of the carboxypeptidase responsible for the post-synthetic modification of creatine kinase in human serumD Hendriks, J Soons, S Scharpé, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1970
[Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]H G Terheggen, A Schwenk, A Lowenthal, et al.
Journal De Genetique Humaine|March 1, 1972
Familial hyperargininemiaH G Terheggen, F Lavinha, J P Colombo, et al.
Biochimie|January 1, 1991
Proteases and their inhibitors: today and tomorrowS Scharpe, I De Meester, D Hendriks, et al.
Biochemical Society Transactions|August 1, 1990
Dipeptidyl peptidase IV in human lymphocytes: molecular propertiesI de Meester, G Vanhoof, S Scharpé, et al.
Urologia Internationalis|January 1, 1985
Tripeptidyl carboxypeptidase activity of angiotensin-converting enzyme in human tissues of the urogenital tractM van Sande, J Inokuchi, A Nagamatsu, et al.
Pageof 6