M A Kroos - JoVE Visualize

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The Journal of Biological Chemistry|May 2, 1997

Endogenous type II cGMP-dependent protein kinase exists as a dimer in membranes and can Be functionally distinguished from the type I isoformsA B Vaandrager, M Edixhoven, A G Bot, et al.

Biochemical and Biophysical Research Communications|September 30, 1994

Deletion of exon 18 is a frequent mutation in glycogen storage disease type IIM Van der Kraan, M A Kroos, M Joosse, 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.

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.

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.

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.

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.

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Showing results (21-30 of 42) with videos related to

Sort By:

Pageof 5

The Journal of Biological Chemistry|May 2, 1997

Endogenous type II cGMP-dependent protein kinase exists as a dimer in membranes and can Be functionally distinguished from the type I isoformsA B Vaandrager, M Edixhoven, A G Bot, et al.

Biochemical and Biophysical Research Communications|September 30, 1994

Deletion of exon 18 is a frequent mutation in glycogen storage disease type IIM Van der Kraan, M A Kroos, M Joosse, 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.

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.

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.

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.

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.

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