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The Biochemical Journal|December 1, 1990
Expression and routeing of human lysosomal alpha-glucosidase in transiently transfected mammalian cellsL H Hoefsloot, R Willemsen, M A Kroos, et al.Nature|June 24, 1993
Characterization and localization of the FMR-1 gene product associated with fragile X syndromeC Verheij, C E Bakker, E de Graaff, et al.Human Molecular Genetics|May 1, 1995
Characterization of FMR1 proteins isolated from different tissuesC Verheij, E de Graaff, C E Bakker, et al.Muscle & Nerve. Supplement|January 1, 1995
Glycogenosis type II (acid maltase deficiency)A J Reuser, M A Kroos, M M Hermans, et al.Human Molecular Genetics|December 1, 1994
The effect of a single base pair deletion (delta T525) and a C1634T missense mutation (pro545leu) on the expression of lysosomal alpha-glucosidase in patients with glycogen storage disease type IIM M Hermans, E De Graaff, M A Kroos, et al.JIMD Reports|November 26, 2013
Newborn screening for hunter disease: a small-scale feasibility studyG J G Ruijter, D A Goudriaan, A M Boer, et al.Biochemical and Biophysical Research Communications|February 15, 1993
Biochemical genetics of glycogenosis type II in Brahman cattleH A Wisselaar, M M Hermans, W J Visser, et al.European Journal of Human Genetics : EJHG|September 14, 1999
Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counsellingM G Ausems, J Verbiest, M P Hermans, et al.European Journal of Biochemistry|August 15, 1983
Monoclonal antibodies against human beta-glucocerebrosidaseR A Barneveld, F P Tegelaers, E I Ginns, et al.Human Molecular Genetics|September 16, 1998
Recombinant human acid alpha-glucosidase: high level production in mouse milk, biochemical characteristics, correction of enzyme deficiency in GSDII KO miceA G Bijvoet, M A Kroos, F R Pieper, et al.Pageof 10