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Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A.
Tagawa K, Taya C, Hayashi Y, Nakagawa M, Ono Y, Fukuda R, Karasuyama H, Toyama-Sorimachi N, Katsui Y, Hata S, Ishiura S, Nonaka I, Seyama Y, Arahata K, Yonekawa H, Sorimachi H, Suzuki K. Tagawa K, et al. Hum Mol Genet. 2000 May 22;9(9):1393-402. doi: 10.1093/hmg/9.9.1393. Hum Mol Genet. 2000. PMID: 10814721
Dynamic distribution of muscle-specific calpain in mice has a key role in physical-stress adaptation and is impaired in muscular dystrophy.
Ojima K, Kawabata Y, Nakao H, Nakao K, Doi N, Kitamura F, Ono Y, Hata S, Suzuki H, Kawahara H, Bogomolovas J, Witt C, Ottenheijm C, Labeit S, Granzier H, Toyama-Sorimachi N, Sorimachi M, Suzuki K, Maeda T, Abe K, Aiba A, Sorimachi H. Ojima K, et al. J Clin Invest. 2010 Aug;120(8):2672-83. doi: 10.1172/JCI40658. Epub 2010 Jul 1. J Clin Invest. 2010. PMID: 20592470 Free PMC article.
Collaboration between a cis-interacting natural killer cell receptor and membrane sphingolipid is critical for the phagocyte function.
Karyu H, Niki T, Sorimachi Y, Hata S, Shimabukuro-Demoto S, Hirabayashi T, Mukai K, Kasahara K, Takubo K, Goda N, Honke K, Taguchi T, Sorimachi H, Toyama-Sorimachi N. Karyu H, et al. Among authors: toyama sorimachi n. Front Immunol. 2024 Apr 24;15:1401294. doi: 10.3389/fimmu.2024.1401294. eCollection 2024. Front Immunol. 2024. PMID: 38720899 Free PMC article.
80 results