M. Yoshida

发表

Heterogeneity of dystrophin-associated proteins.

H. Yamamoto, Y. Mizuno, Y. Hagiwara, 1993, Journal of biochemistry.

Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.

H. Hama, T. Sasaoka, S. Noguchi, 1999, Human molecular genetics.

Proteinase-sensitive sites on isolated rabbit dystrophin.

E. Ozawa, M. Yoshida, T. Shimizu, 1992, Journal of biochemistry.

Developmental expression of sarcoglycan gene products in cultured myocytes.

S. Noguchi, E. Ozawa, Mikiharu Yoshida, 1999, Biochemical and biophysical research communications.

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.

J. Vance, L. Middleton, I. Nonaka, 1995, Science.

The Frequency of Patients With 50-kd Dystrophin-Associated Glycoprotein (50DAG or adhalin) Deficiency in a Muscular Dystrophy Patient Population in Japan

I. Nonaka, Y. Hayashi, K. Arahata, 1995, Neurology.

Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.

L. Kunkel, E. McNally, E. Ozawa, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Dystrophin-associated proteins in muscular dystrophy.

S. Noguchi, E. Ozawa, Y. Mizuno, 1995, Human molecular genetics.

From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy

S. Noguchi, E. Ozawa, Y. Mizuno, 1998, Muscle & nerve.

Glycoprotein complex anchoring dystrophin to sarcolemma.

E. Ozawa, M. Yoshida, 1990, Journal of biochemistry.

Formation of sarcoglycan complex with differentiation in cultured myocytes.

S. Noguchi, E. Ozawa, M. Imamura, 2000, European journal of biochemistry.

Sarcoglycan complex is selectively lost in dystrophic hamster muscle.

I. Nonaka, H. Yamamoto, S. Noguchi, 1995, The American journal of pathology.

Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice- prone region of the dystrophin COOH terminus

E. Ozawa, M. Yoshida, A. Suzuki, 1995, The Journal of cell biology.

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin.

Kensuke Hayashi, E. Ozawa, Y. Mizuno, 1994, European journal of biochemistry.

Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy.

H. Hama, T. Sasaoka, S. Noguchi, 2000, Human molecular genetics.

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.

L. Kunkel, S. Selig, M. Anderson, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside.

H. Yamamoto, S. Noguchi, Y. Mizuno, 1994, European journal of biochemistry.

Distribution of dystrophin isoforms and dystrophin-associated proteins 43DAG (A3a) and 50DAG (A2) in various monkey tissues.

H. Yamamoto, Y. Mizuno, S. Hirai, 1993, Journal of biochemistry.

A dystrophin-associated glycoprotein, A3a (one of 43DAG doublets), is retained in Duchenne muscular dystrophy muscle.

I. Nonaka, E. Ozawa, Y. Mizuno, 1993, Journal of biochemistry.

Detection of dystrophin on two-dimensional gel electrophoresis.

H. Sugiura, T. Shimizu, T. Hirabayashi, 1989, Biochemical and biophysical research communications.

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.

I. Nonaka, Y. Hayashi, H. Yamamoto, 1994, Biochemical and biophysical research communications.

Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart

M. Shigekawa, Y. Iwata, Y. Mizuno, 1993, FEBS letters.

Expression of dystrophin-associated protein 35DAG (A4) and 50DAG (A2) is confined to striated muscles.

I. Nonaka, H. Yamamoto, Y. Mizuno, 1994, Journal of biochemistry.