T. Shimizu

发表

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin.

I. Kanazawa, S. Kusunoki, K. Matsumura, 1997, The Journal of biological chemistry.

Conformational changes in mutant lysozymes detected with monoclonal antibody

A. Kato, T. Shimizu, S. Saga, 1995, FEBS letters.

A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

K. Matsumura, F. Saito, H. Tomimitsu, 2004, Neuromuscular Disorders.

Localization of C-protein isoforms in chicken skeletal muscle: ultrastructural detection using monoclonal antibodies

J. Dennis, F. Reinach, D. Fischman, 1984, The Journal of cell biology.

Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity.

Y. Sunada, K. Matsumura, S. Arata, 2001, Human molecular genetics.

Heterogeneity of type 1 skeletal muscle fibers revealed by monoclonal antibody to slow myosin

S. Shafiq, D. Fischman, Teruo Shimizu, 1984, Muscle & nerve.

Cross‐reactivity of an antineurofilament antibody with a troponin‐T isoform

H. Kawahara, K. Kohama, Toshitaka Nakamura, 1989, Muscle & nerve.

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33

I. Kanazawa, Y. Nakamura, I. Nonaka, 1993, Nature Genetics.

Three‐dimensional MR imaging of brain surface anomalies in fukuyama‐type congenital muscular dystrophy

I. Kanazawa, K. Matsumura, Y. Sunada, 1995, Muscle & nerve.

Expression of dystroglycan and laminin-2 in peripheral nerve under axonal degeneration and regeneration

Y. Sunada, K. Matsumura, T. Masaki, 2000, Acta Neuropathologica.

Axial arrangement of the myosin rod in vertebrate thick filaments: immunoelectron microscopy with a monoclonal antibody to light meromyosin

J. Dennis, D. Fischman, T. Masaki, 1985, The Journal of cell biology.

Analysis of the metal-induced conformational change in myosin with a monoclonal antibody to light chain two.

F. Reinach, D. Fischman, T. Masaki, 1985, Journal of molecular biology.

Processing of beta-dystroglycan by matrix metalloproteinase disrupts the link between the extracellular matrix and cell membrane via the dystroglycan complex.

K. Matsumura, F. Saito, R. Maekawa, 2001, Human molecular genetics.

The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation.

Y. Sunada, K. Matsumura, F. Saito, 1997, Histology and histopathology.

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

K. Campbell, S. Roberds, M. Nakagawa, 1994, The Journal of clinical investigation.

Expression of dystroglycan complex in satellite cells of dorsal root ganglia

K. Matsumura, A. Hirata, T. Masaki, 2001, Acta Neuropathologica.

Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?

Y. Sunada, K. Matsumura, F. Saito, 1999, Cellular and molecular biology.

Molecular cloning and expression dynamics of UNC-45B upon heat shock in the muscle of yellowtail

Yi-Li Gao, K. Osatomi, Asami Yoshida, 2021 .

Inhibition of proteolytic activity of calcium activated neutral protease by leupeptin and antipain.

T. Toyo-Oka, T. Shimizu, T. Masaki, 1978, Biochemical and biophysical research communications.