Ichizo Nishino - Dissemin

Papers authored by Ichizo Nishino

This paper was not found in any repository, but could be made available legally by the author.

2014 Koichi Ojima, Yasuko Ono, Shoji Hata, Satoru Noguchi, Ichizo Nishino

, Hiroyuki Sorimachi

Muscle-specific calpain-3 is phosphorylated in its unique insertion region for enrichment in a myofibril fraction

Upload

Yukari Endo, Satoru Noguchi, Yuji Hara, Yukiko K. Hayashi, Kazushi Motomura, Satoko Miyatake, Nobuyuki Murakami, Satsuki Tanaka, Sumimasa Yamashita, Rika Kizu, Masahiro Bamba, Yu-Ichi Goto, Naomichi Matsumoto, Ikuya Nonaka, Ichizo Nishino

Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca2+ channels

Upload

Shigeaki Suzuki, Takahiro Yonekawa, Masataka Kuwana, Yukiko K. Hayashi, Yuka Okazaki, Yasushi Kawaguchi, Norihiro Suzuki, Ichizo Nishino

Clinical and histological findings associated with autoantibodies detected by RNA immunoprecipitation in inflammatory myopathies

Upload

Shin-Ichi Uchiyama

, Ichizo Nishino

, Tatsuro Izumi

The muscle findings in a pediatric patient with live attenuated oral polio vaccine-related flaccid monoplegia

Upload

Jantima Tanboon, Yukiko K. Hayashi, Ichizo Nishino

, Tumtip Sangruchi

Kyphoscoliosis and easy fatigability in a 14-year-old boy

Upload

Hirotomo Saitsu, Jun Tohyama, Tom Walsh, Mitsuhiro Kato, Yu Kobayashi, Ming Lee, Yoshinori Tsurusaki, Noriko Miyake, Yu-Ichi Goto, Ichizo Nishino

, Akira Ohtake, Mary-Claire King, Naomichi Matsumoto

A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation

Upload

Takayuki Fujii, Shintaro Hayashi, Nobutoshi Kawamura, Masa-Aki Higuchi, Jun Tsugawa, Yasumasa Ohyagi, Yukiko K. Hayashi

, Ichizo Nishino

, Jun-Ichi Kira

A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles

Upload

Takahiro Yonekawa, May Christine V. Malicdan, Anna Cho, Yukiko K. Hayashi, Ikuya Nonaka, Toshiki Mine, Takeshi Yamamoto, Ichizo Nishino

, Satoru Noguchi

Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice

Upload

Ichizo Nishino

, Nuria Carrillo-Carrasco

, Zohar Argov

GNE myopathy: current update and future therapy

Upload

Satoko Miyatake, Eriko Koshimizu, Yukiko K. Hayashi, Kazushi Miya, Masaaki Shiina, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Kazuhiro Ogata, Ichizo Nishino

, Naomichi Matsumoto

Deep sequencing detects very-low-grade somatic mosaicism in the unaffected mother of siblings with nemaline myopathy

Upload

T. Yonekawa, I. Nishino

Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s)

Upload

Luciano Merlini, Ichizo Nishino

201st ENMC International Workshop: Autophagy in muscular dystrophies – Translational approach, 1–3 November 2013, Bussum, The Netherlands

Upload

Madoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, Naohiro Yonemoto, Yoko Kobayashi, Yukiko K. Hayashi, Satoru Noguchi, Ichizo Nishino

, Miho Murata

GNE myopathy: A prospective natural history study of disease progression

Upload

Sachiko Kajino, Kayo Ishihara, Kanako Goto, Keiko Ishigaki, Satoru Noguchi, Ikuya Nonaka, Makiko Osawa, Ichizo Nishino

, Yukiko K. Hayashi

Congenital fiber type disproportion myopathy caused by LMNA mutations

Upload

Marjan Huizing, Nuria Carrillo-Carrasco, May Christine V. Malicdan, Satoru Noguchi, William A. Gahl, Stella Mitrani-Rosenbaum, Zohar Argov, Ichizo Nishino

GNE myopathy: New name and new mutation nomenclature

Upload

A. Uezumi, S. Fukada, N. Yamamoto, M. Ikemoto-Uezumi, M. Nakatani, M. Morita, A. Yamaguchi, H. Yamada, I. Nishino

, Y. Hamada, K. Tsuchida

Identification and characterization of PDGFRα+ mesenchymal progenitors in human skeletal muscle

Upload

This paper is made freely available by the publisher.

Tomoko Sugiura, Yasushi Kawaguchi, Kanako Goto, Yukiko Hayashi, Takahisa Gono, Takefumi Furuya, Ichizo Nishino

, Hisashi Yamanaka

Association between a C8orf13–BLK Polymorphism and Polymyositis/Dermatomyositis in the Japanese Population: An Additive Effect with STAT4 on Disease Susceptibility

Download from doi.org

Raj Poovindran Anada, Kum Thong Wong, May Christine Malicdan, Khean Jin Goh, Yukiko Hayashi, Ichizo Nishino

, Satoru Noguchi

Absence of beta-amyloid deposition in the central nervous system of a transgenic mouse model of distal myopathy with rimmed vacuoles

Upload

Masahide Goto, Hirofumi Komaki, Takashi Saito, Yoshiaki Saito, Eiji Nakagawa, Kenji Sugai, Masayuki Sasaki, Ichizo Nishino

, Yu-Ichi Goto

MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene

Upload

Takahiro Nakayama, Harumasa Nakamura, Yasushi Oya, Takashi Kimura, Ichiro Imahuku, Kinji Ohno, Ichizo Nishino

, Koji Abe, Tohru Matsuura

Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2

Upload

Missing publications? Search for publications with a matching author name.

Researcher

Statistics

Refine

Papers authored by Ichizo Nishino