Ichizo Nishino - Dissemin

Papers authored by Ichizo Nishino

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2008 Chie Matsuda, Kimihiko Kameyama, Atsushi Suzuki, Wataru Mishima, Satoshi Yamaji, Harumasa Okamoto, Ichizo Nishino

, Yukiko K. Hayashi

Affixin activates Rac1 via βPIX in C2C12 myoblast

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Takahiro Tanabe, Makoto Fukusaki, Yoshiaki Terao, Kazunori Yamashita, Koji Sumikawa, Keiko Mukaida, Carlos A. Ibarra, Ichizo Nishino

Malignant hyperthermia susceptibility diagnosed with a family-specific ryanodine receptor gene type 1 mutation

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T. Tuñón, D. Guerrero, A. Urchaga, I. Nishino

, T. Ayuso, Y. Matsuda, M. C. Caballero, J. Berjón, M. A. Imizcoz

Danon disease: A novel Lamp-2 gene mutation in a family with four affected members

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M. Astejada, M. C. Malicdan, I. Nishino

Muscular Dystrophies

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Minoru Oishi, Kenji Miki, Akihiko Morita, Kazumi Fujioka, Shigeki Aoki, Ichizo Nishino

, Ikuya Nonaka, Yu-Ichi Goto, Tomohiko Mizutani

Mitochondrial Encephalomyopathy Associated with Diabetes Mellitus, Cataract, and Corpus Callosum Atrophy

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Satomi Okahashi, Go Ogawa, Mikiya Suzuki, Katsuhisa Ogata, Ichizo Nishino

, Mitsuru Kawai

Asymptomatic Sporadic Dysferlinopathy Presenting with Elevation of Serum Creatine Kinase. Typical Distribution of Muscle Involvement Shown by MRI but not by CT

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This paper is made freely available by the publisher.

Ichizo Nishino

, Chieko Fujimura-Kiyono, GaborZ Racz

Myotubular/centronuclear myopathy and central core disease

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2007 I. Eisenberg, A. Eran, I. Nishino

, M. Moggio, C. Lamperti, A. A. Amato, H. G. Lidov, P. B. Kang, K. N. North, S. Mitrani-Rosenbaum, K. M. Flanigan, L. A. Neely, D. Whitney, A. H. Beggs, I. S. Kohane and 1 other authors

Distinctive patterns of microRNA expression in primary muscular disorders

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G. Kawahara, M. Okada, N. Morone, C. A. Ibarra, I. Nonaka, S. Noguchi, Y. K. Hayashi, I. Nishino

Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease

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M. Okada, G. Kawahara, S. Noguchi, K. Sugie, K. Murayama, I. Nonaka, Y. K. Hayashi, I. Nishino

Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan

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J. Aoki, T. Yasuno, H. Sugie, H. Kido, I. Nishino

, Y. Shigematsu, M. Kanazawa, M. Takayanagi, M. Kumami, K. Endo, H. Kaneoka, M. Yamaguchi, T. Fukuda, T. Yamamoto

A Japanese Adult Form of Cpt Ii Deficiency Associated With a Homozygous F383y Mutation

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E. Matsubara, A. Tsuchiya, N. Minami, I. Nishino

, M. A. Pappolla, M. Shoji, K. Abe

A unique case of limb-girdle muscular dystrophy type 2A carrying novel compound heterozygous mutations in the human CAPN3 gene

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Shigehisa Ura, Yukiko K. Hayashi, Kanako Goto, Mina Nolasco Astejada, Terumi Murakami, Masako Nagato, Shigeru Ohta, Yasuhisa Daimon, Hidehiro Takekawa, Koichi Hirata, Ikuya Nonaka, Satoru Noguchi, Ichizo Nishino

Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations

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M. C. V. Malicdan, S. Noguchi, I. Nonaka, Y. K. Hayashi, I. Nishino

A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

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M. C. V. Malicdan, S. Noguchi, I. Nonaka, Y. K. Hayashi, I. Nishino

A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

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I. Sato, S. Wu, M. C. A. Ibarra, Y. K. Hayashi, H. Fujita, M. Tojo, S. J. Oh, I. Nonaka, S. Noguchi, I. Nishino

Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation

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Yi-Ching Lin, Terumi Murakami, Yukiko K. Hayashi, Ichizo Nishino

, Ikuya Nonaka, Chung-Yee Yuo, Yuh-Jyh Jong

A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2I

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Yoko Keira, Satoru Noguchi, Rumi Kurokawa, Masako Fujita, Narihiro Minami, Yukiko K. Hayashi, Takashi Kato, Ichizo Nishino

Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling

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Yuriko Nezu, Yoshihiro Kino, Noboru Sasagawa, Ichizo Nishino

, Shoichi Ishiura

Expression of MBNL and CELF mRNA transcripts in muscles with myotonic dystrophy

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Maki Ohsawa, Teerin Liewluck, Katuhisa Ogata, Takahiro Iizuka, Yukiko Hayashi, Ikuya Nonaka, Masayuki Sasaki, Ichizo Nishino

Familial reducing body myopathy

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Papers authored by Ichizo Nishino