S Fukuda|K Sukegawa|S Tomatsu|T Orii - JoVE Visualize

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Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995

[Mucopolysaccharidoses]S Fukuda, K Sukegawa, S Tomatsu, et al.

Nihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1993

[Mucopolysaccharidosis type VII: characterization of exonic point mutations and molecular heterogeneity]T Orii, S Tomatsu, S Fukuda, et al.

Journal of Biochemistry|November 1, 1991

Purification and partial characterization of alpha-N-acetylglucosaminidase from human liverT Sasaki, K Sukegawa, M Masue, et al.

Human Genetics|January 1, 1990

Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.

The Journal of Biological Chemistry|September 23, 1994

Overexpression rescues the mutant phenotype of L176F mutation causing beta-glucuronidase deficiency mucopolysaccharidosis in two Mennonite siblingsB M Wu, S Tomatsu, S Fukuda, et al.

Rinsho Byori. the Japanese Journal of Clinical Pathology|September 1, 1990

[Molecular basis of mucopolysaccaridosis type VII (beta-glucuronidase deficiency)]S Tomatsu, S Fukuda, K Sukegawa, et al.

Genomics|June 1, 1993

Mucopolysaccharidosis IV A: assignment of the human N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene to chromosome 16q24M Masuno, S Tomatsu, Y Nakashima, et al.

Cell Structure and Function|April 1, 1992

Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)H Okamoto, K Sukegawa, S Tomatsu, et al.

Human Mutation|January 1, 1996

Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsA Yamagishi, S Tomatsu, S Fukuda, et al.

Gene|May 14, 1990

Molecular basis of mucopolysaccharidosis type VII: replacement of Ala619 in beta-glucuronidase with ValS Tomatsu, K Sukegawa, Y Ikedo, et al.

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Pageof 104

Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995

[Mucopolysaccharidoses]S Fukuda, K Sukegawa, S Tomatsu, et al.

Nihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1993

[Mucopolysaccharidosis type VII: characterization of exonic point mutations and molecular heterogeneity]T Orii, S Tomatsu, S Fukuda, et al.

Journal of Biochemistry|November 1, 1991

Purification and partial characterization of alpha-N-acetylglucosaminidase from human liverT Sasaki, K Sukegawa, M Masue, et al.

Human Genetics|January 1, 1990

Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.

The Journal of Biological Chemistry|September 23, 1994

Overexpression rescues the mutant phenotype of L176F mutation causing beta-glucuronidase deficiency mucopolysaccharidosis in two Mennonite siblingsB M Wu, S Tomatsu, S Fukuda, et al.

Rinsho Byori. the Japanese Journal of Clinical Pathology|September 1, 1990

[Molecular basis of mucopolysaccaridosis type VII (beta-glucuronidase deficiency)]S Tomatsu, S Fukuda, K Sukegawa, et al.

Genomics|June 1, 1993

Mucopolysaccharidosis IV A: assignment of the human N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene to chromosome 16q24M Masuno, S Tomatsu, Y Nakashima, et al.

Cell Structure and Function|April 1, 1992

Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)H Okamoto, K Sukegawa, S Tomatsu, et al.

Human Mutation|January 1, 1996

Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsA Yamagishi, S Tomatsu, S Fukuda, et al.

Gene|May 14, 1990

Molecular basis of mucopolysaccharidosis type VII: replacement of Ala619 in beta-glucuronidase with ValS Tomatsu, K Sukegawa, Y Ikedo, et al.

Pageof 104