A J Reuser - JoVE Visualize

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Biochemical and Biophysical Research Communications|March 29, 1991

Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiencyP Hu, A J Reuser, H C Janse, et al.

European Journal of Biochemistry|March 15, 1984

Use of a monoclonal antibody to distinguish between precursor and mature forms of human lysosomal alpha-glucosidaseR P Oude Elferink, A Strijland, I Surya, et al.

European Journal of Human Genetics : EJHG|January 10, 2002

Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.

Pediatric Research|October 1, 1990

Rat heart perfusion as model system for enzyme replacement therapy in glycogenosis type IIA T van der Ploeg, A M van der Kraaij, R Willemsen, et al.

Clinical Genetics|June 1, 1996

Homozygous deletion of exon 18 leads to degradation of the lysosomal alpha-glucosidase precursor and to the infantile form of glycogen storage disease type IIM G Ausems, M A Kroos, M Van der Kraan, et al.

Journal of Neurology|January 1, 1987

Ultrastructural localization of glucocerebrosidase in cultured Gaucher's disease fibroblasts by immunocytochemistryR Willemsen, J M van Dongen, E I Ginns, et al.

Experimental Cell Research|November 1, 1984

Uptake and stability of human and bovine acid alpha-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patientsA J Reuser, M A Kroos, N J Ponne, et al.

Biochimica Et Biophysica Acta|August 14, 1996

Expression of cDNA-encoded human acid alpha-glucosidase in milk of transgenic miceA G Bijvoet, M A Kroos, F R Pieper, et al.

Molecular and Chemical Neuropathology|February 1, 1995

A biochemical and ultrastructural evaluation of the type 2 Gaucher mouseR Willemsen, V Tybulewicz, E Sidransky, et al.

Pediatric Research|July 1, 1995

Prenatal diagnosis of glycogen storage disease type II: enzyme assay or mutation analysis?W J Kleijer, M van der Kraan, M A Kroos, et al.

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Showing results (71-80 of 98) with videos related to

Sort By:

Pageof 10

Biochemical and Biophysical Research Communications|March 29, 1991

Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiencyP Hu, A J Reuser, H C Janse, et al.

European Journal of Biochemistry|March 15, 1984

Use of a monoclonal antibody to distinguish between precursor and mature forms of human lysosomal alpha-glucosidaseR P Oude Elferink, A Strijland, I Surya, et al.

European Journal of Human Genetics : EJHG|January 10, 2002

Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.

Pediatric Research|October 1, 1990

Rat heart perfusion as model system for enzyme replacement therapy in glycogenosis type IIA T van der Ploeg, A M van der Kraaij, R Willemsen, et al.

Clinical Genetics|June 1, 1996

Homozygous deletion of exon 18 leads to degradation of the lysosomal alpha-glucosidase precursor and to the infantile form of glycogen storage disease type IIM G Ausems, M A Kroos, M Van der Kraan, et al.

Journal of Neurology|January 1, 1987

Ultrastructural localization of glucocerebrosidase in cultured Gaucher's disease fibroblasts by immunocytochemistryR Willemsen, J M van Dongen, E I Ginns, et al.

Experimental Cell Research|November 1, 1984

Uptake and stability of human and bovine acid alpha-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patientsA J Reuser, M A Kroos, N J Ponne, et al.

Biochimica Et Biophysica Acta|August 14, 1996

Expression of cDNA-encoded human acid alpha-glucosidase in milk of transgenic miceA G Bijvoet, M A Kroos, F R Pieper, et al.

Molecular and Chemical Neuropathology|February 1, 1995

A biochemical and ultrastructural evaluation of the type 2 Gaucher mouseR Willemsen, V Tybulewicz, E Sidransky, et al.

Pediatric Research|July 1, 1995

Prenatal diagnosis of glycogen storage disease type II: enzyme assay or mutation analysis?W J Kleijer, M van der Kraan, M A Kroos, et al.

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