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American Journal of Human Genetics|March 1, 1978
Biochemical, immunological, and cell genetic studies in glycogenosis type IIA J Reuser, J F Koster, A Hoogeveen, et al.Clinical Genetics|August 1, 1984
Combined sialidase (neuraminidase) and beta-galactosidase deficiency. Clinical, morphological and enzymological observations in a patientM C Loonen, A J Reuser, P Visser, et al.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.Annales De Biologie Clinique|January 1, 1994
Lysosomal storage diseases: cellular pathology, clinical and genetic heterogeneity, therapyA J Reuser, M A Kroos, W J Visser, et al.Biochemical and Biophysical Research Communications|January 13, 1998
Mutation detection in glycogen storage-disease type II by RT-PCR and automated sequencingM M Hermans, D van Leenen, M A Kroos, et al.The Biochemical Journal|February 15, 1996
Lysosomal alpha-glucosidase: cell-specific processing and altered maturation in HT-29 colon cancer cellsC Francí, G Egea, R Arribas, et al.The Biochemical Journal|December 1, 1990
Characterization of the human lysosomal alpha-glucosidase geneL H Hoefsloot, M Hoogeveen-Westerveld, A J Reuser, et al.The Journal of Biological Chemistry|July 15, 1985
Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type IIA J Reuser, M Kroos, R P Oude Elferink, et al.Human Genetics|December 23, 1977
Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybridsH L Hoeksema, A J Reuser, A T Hoogeveen, et al.Human Genetics|January 1, 1985
Cotransfer of syntenic human genes into mouse cells using isolated metaphase chromosomes or cellular DNAA J de Jonge, S de Smit, M A Kroos, et al.Pageof 10