N. Takiyama

发表

Gaucher's disease: studies of gene transfer to haematopoietic cells.

W. Swaney, A. Bahnson, J. Barranger, 1997, Bailliere's clinical haematology.

Four-digit allele genotyping of the HLA-A and HLA-B genes in Japanese patients with Behcet's disease by a PCR-SSOP-Luminex method.

Jerzy K. Kulski, H. Inoko, S. Ohno, 2006, Tissue antigens.

Comparison of methods for retroviral mediated transfer of glucocerebrosidase gene to CD34+ hematopoietic progenitor cells

W. Swaney, A. Bahnson, J. Barranger, 1998, European journal of haematology.

Retrovirus-mediated transfer of human alpha-galactosidase A gene to human CD34+ hematopoietic progenitor cells.

H. Sakuraba, R. Kase, J. Dunigan, 1999, Human gene therapy.

Acid carboxypeptidase deficiency in galactosialidosis

Yoshiyuki Suzuki, A. Oshima, Y. Nagao, 1991, Japanese Journal of Human Genetics.

Characterization of an anti-beta-galactosidase antibody recognizing a precursor but not a mature enzyme in solution.

A. Oshima, Y. Suzuki, H. Sakuraba, 1993, Biochemical and biophysical research communications.

Molecular form and subcellular distribution of acid β-galactosidase in fibroblasts from patients with GM1 gangliosidosis, Morquio B disease and galactosialidosis

Hitoshi Sakuraba, Yoshiyuki Suzuki, H. Sakuraba, 1997, Brain and Development.

Development of Gene Therapy for Gaucher Disease

W. Swaney, A. Bahnson, J. Barranger, 2002 .

Enzyme reactor for urinary acylcarnitines assay by reversed-phase high-performance liquid chromatography.

Mamoru Takahashi, H. Misaki, Kojiro Matsumoto, 1993, Clinica chimica acta; international journal of clinical chemistry.

Galactosialidosis: simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities.

A. Oshima, Y. Suzuki, H. Sakuraba, 1990, Biochemical and biophysical research communications.

Galactosialidosis : clinical and molecular analysis of 19 Japanese patients

A. Oshima, Y. Suzuki, T. Kobayashi, 1991 .