M A Kroos - JoVE Visualize

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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.

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.

Annals of Human Genetics|May 1, 1989

An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type IIA T Van der Ploeg, M A Kroos, D M Swallow, et al.

Clinical Genetics|July 11, 1998

Glycogen storage disease type II: identification of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase geneM A Kroos, D van Leenen, J Verbiest, et al.

Biochimica Et Biophysica Acta|November 20, 1987

Cell-free translation of human lysosomal alpha-glucosidase: evidence for reduced precursor synthesis in an adult patient with glycogenosis type IIG T van der Horst, E H Hoefsloot, M A Kroos, et al.

Human Mutation|January 1, 1993

Two mutations affecting the transport and maturation of lysosomal alpha-glucosidase in an adult case of glycogen storage disease type IIM M Hermans, M A Kroos, E de Graaff, et al.

The Journal of Biological Chemistry|January 25, 1993

Structural and functional changes of lysosomal acid alpha-glucosidase during intracellular transport and maturationH A Wisselaar, M A Kroos, M M Hermans, et al.

The Journal of Biological Chemistry|July 25, 1991

Human lysosomal alpha-glucosidase. Characterization of the catalytic siteM M Hermans, M A Kroos, J van Beeumen, et al.

The Biochemical Journal|February 1, 1993

Human lysosomal alpha-glucosidase: functional characterization of the glycosylation sitesM M Hermans, H A Wisselaar, M A Kroos, et al.

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Showing results (1-10 of 42) with videos related to

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Pageof 5

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.

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.

Annals of Human Genetics|May 1, 1989

An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type IIA T Van der Ploeg, M A Kroos, D M Swallow, et al.

Clinical Genetics|July 11, 1998

Glycogen storage disease type II: identification of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase geneM A Kroos, D van Leenen, J Verbiest, et al.

Biochimica Et Biophysica Acta|November 20, 1987

Cell-free translation of human lysosomal alpha-glucosidase: evidence for reduced precursor synthesis in an adult patient with glycogenosis type IIG T van der Horst, E H Hoefsloot, M A Kroos, et al.

Human Mutation|January 1, 1993

Two mutations affecting the transport and maturation of lysosomal alpha-glucosidase in an adult case of glycogen storage disease type IIM M Hermans, M A Kroos, E de Graaff, et al.

The Journal of Biological Chemistry|January 25, 1993

Structural and functional changes of lysosomal acid alpha-glucosidase during intracellular transport and maturationH A Wisselaar, M A Kroos, M M Hermans, et al.

The Journal of Biological Chemistry|July 25, 1991

Human lysosomal alpha-glucosidase. Characterization of the catalytic siteM M Hermans, M A Kroos, J van Beeumen, et al.

The Biochemical Journal|February 1, 1993

Human lysosomal alpha-glucosidase: functional characterization of the glycosylation sitesM M Hermans, H A Wisselaar, M A Kroos, et al.

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