A. Tanaka

发表

Characterization of full‐length cDNAs and the gene coding for the human GM2 activator protein

K. Sandhoff, M. Schröder, Kunihiko Suzuki, 1991, FEBS letters.

GM2-Gangliosidosis BI Variant: Analysis of I-Hexosaminidase a Gene Abnormalities in Seven Patients

K. Sandhoff, E. Kolodny, A. Brown, 2006 .

A new point mutation within exon 5 of β‐hexosaminidase α gene in a Japanese infant with Tay‐Sachs disease

Yoshiyuki Suzuki, E. Nanba, K. Ohno, 1990 .

GM2-Gangliosidosis B I Variant: Analysis of 1-Hexosaminidase a Gene Mutations in I I Patients from a Defined Region in Portugal

Sá, M. G. Ribeiro, M. R. Santos, 2006 .

A new point mutation in the beta-hexosaminidase alpha subunit gene responsible for infantile Tay-Sachs disease in a non-Jewish Caucasian patient (a Kpn mutant).

K. Suzuki, H. Punnett, A. Tanaka, 1990, American journal of human genetics.

Immunofluorescence staining and immunological studies of arylsulphatase a of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts

G. Isshiki, M. Furusawa, T. Matsumoto, 1983, Journal of Inherited Metabolic Disease.

Western blotting analysis of the β‐hexosaminidase α‐ and β‐subunits in cultured fibroblasts from cases of various forms of GM2 gangliosidosis

A. Tsuji, E. Uyama, H. Sakuraba, 2002, Acta neurologica Scandinavica.

Genetic cause of a juvenile form of tay‐sachs disease in a lebanese child

R. Boustany, K. Suzuki, Kunihiko Suzuki, 1991, Annals of neurology.

Determination of urinary lysozyme for potential detection of tubular dysfunction in diabetic nephropathy.

K. Shima, M. Hirota, M. Fukuda, 1986, Clinical chemistry.

Two mutations remote from an exon/intron junction in the β-hexosaminidase β-subunit gene affect 3’-splice site selection and cause Sandhoff disease

G. Isshiki, H. Sakuraba, N. Wakamatsu, 1998, Human Genetics.

GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene mutations in 11 patients from a defined region in Portugal.

M. Ribeiro, K. Suzuki, M. S. Sá Miranda, 1991, American journal of human genetics.

GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene abnormalities in seven patients.

A. Brown, K. Sandhoff, K. Suzuki, 1990, American journal of human genetics.

GM2-gangliosidosis B1 variant: A wide geographic and ethnic distribution of the specific β-hexosaminidase α chain mutation originally identified in a puerto rican patient*

K. Ohno, Kunihiko Suzuki, A. Tanaka, 1988 .

Molecular genetics of Tay-Sachs disease in Japan

G. Isshiki, K. Suzuki, H. Murakami, 1994, Journal of Inherited Metabolic Disease.

Complementation studies with clinical and biochemical characterizations of a new variant of multiple sulphatase deficiency

M. Ishii, G. Isshiki, M. Nishida, 1987, Journal of Inherited Metabolic Disease.

Variation of lysosomal enzyme activity with gestational age in chorionic villi

G. Isshiki, M. Fukuda, A. Tanaka, 1990, Journal of Inherited Metabolic Disease.

Copper-binding proteins in the liver and kidney from the patients with Menkes' kinky hair disease.

M. Hirose, G. Isshiki, Y. Kojima, 1983, Tohoku journal of experimental medicine.

Two mutations remote from an exon/intron junction in the beta-hexosaminidase beta-subunit gene affect 3'-splice site selection and cause Sandhoff disease.

G. Isshiki, H. Sakuraba, N. Wakamatsu, 1998, Human Genetics.

A New Point Mutation in the 0-Hexosaminidase a Subunit Gene Responsible for Infantile Tay-Sachs Disease in a Non-Jewish Caucasian Patient (a Kpn Mutant)

A. Tanaka, Hope H. Punnettt, Kunihiko Suzuki, 2006 .

Expression of the beta-hexosaminidase alpha subunit gene with the four-base insertion of infantile Jewish Tay-Sachs disease.

E. Nanba, J. Nishimoto, A. Tanaka, 1991, The Journal of biological chemistry.

GM2-gangliosidosis B1 variant: a wide geographic and ethnic distribution of the specific beta-hexosaminidase alpha chain mutation originally identified in a Puerto Rican patient.

K. Ohno, A. Tanaka, K. Suzuki, 1988, Biochemical and biophysical research communications.