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Zmynd17 controls muscle mitochondrial quality and whole-body metabolism.
Fujita R, Yoshioka K, Seko D, Suematsu T, Mitsuhashi S, Senoo N, Miura S, Nishino I, Ono Y. Fujita R, et al. Among authors: nishino i. FASEB J. 2018 Sep;32(9):5012-5025. doi: 10.1096/fj.201701264R. Epub 2018 Apr 13. FASEB J. 2018. PMID: 29913553
., Seko, D., Suematsu, T., Mitsuhashi, S., Senoo, N., Miura, S., Nishino, I., Ono, Y. Zmynd17 controls muscle mitochondrial quality and whole-body metabolism....
., Seko, D., Suematsu, T., Mitsuhashi, S., Senoo, N., Miura, S., Nishino, I., Ono, Y. Zmynd17 controls muscle mitochondrial qu …
Skeletal muscle FOXO1 (FKHR) transgenic mice have less skeletal muscle mass, down-regulated Type I (slow twitch/red muscle) fiber genes, and impaired glycemic control.
Kamei Y, Miura S, Suzuki M, Kai Y, Mizukami J, Taniguchi T, Mochida K, Hata T, Matsuda J, Aburatani H, Nishino I, Ezaki O. Kamei Y, et al. Among authors: nishino i. J Biol Chem. 2004 Sep 24;279(39):41114-23. doi: 10.1074/jbc.M400674200. Epub 2004 Jul 21. J Biol Chem. 2004. PMID: 15272020 Free article.
Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification.
Arai A, Mitsuhashi S, Saito Y, Komaki H, Sakuma H, Nakagawa E, Sugai K, Sasaki M, Robertson SP, Nishimura G, Yamamoto T, Nonaka I, Nishino I. Arai A, et al. Among authors: nishino i. Neuromuscul Disord. 2009 Jul;19(7):485-8. doi: 10.1016/j.nmd.2009.06.366. Epub 2009 Jun 23. Neuromuscul Disord. 2009. PMID: 19553121
Distal myopathy in multi-minicore disease.
Mitsuhashi S, Nonaka I, Wu S, Moreno CA, Shalaby S, Hayashi YK, Noguchi S, Nishino I. Mitsuhashi S, et al. Among authors: nishino i. Intern Med. 2009;48(19):1759-62. doi: 10.2169/internalmedicine.48.2425. Epub 2009 Oct 1. Intern Med. 2009. PMID: 19797833 Free article.
The cathepsin L gene is a direct target of FOXO1 in skeletal muscle.
Yamazaki Y, Kamei Y, Sugita S, Akaike F, Kanai S, Miura S, Hirata Y, Troen BR, Kitamura T, Nishino I, Suganami T, Ezaki O, Ogawa Y. Yamazaki Y, et al. Among authors: nishino i. Biochem J. 2010 Mar 15;427(1):171-8. doi: 10.1042/BJ20091346. Biochem J. 2010. PMID: 20088826
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis.
Mitsuhashi S, Ohkuma A, Talim B, Karahashi M, Koumura T, Aoyama C, Kurihara M, Quinlivan R, Sewry C, Mitsuhashi H, Goto K, Koksal B, Kale G, Ikeda K, Taguchi R, Noguchi S, Hayashi YK, Nonaka I, Sher RB, Sugimoto H, Nakagawa Y, Cox GA, Topaloglu H, Nishino I. Mitsuhashi S, et al. Among authors: nishino i. Am J Hum Genet. 2011 Jun 10;88(6):845-851. doi: 10.1016/j.ajhg.2011.05.010. Am J Hum Genet. 2011. PMID: 21665002 Free PMC article.
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.
Mitsuhashi S, Hatakeyama H, Karahashi M, Koumura T, Nonaka I, Hayashi YK, Noguchi S, Sher RB, Nakagawa Y, Manfredi G, Goto Y, Cox GA, Nishino I. Mitsuhashi S, et al. Among authors: nishino i. Hum Mol Genet. 2011 Oct 1;20(19):3841-51. doi: 10.1093/hmg/ddr305. Epub 2011 Jul 12. Hum Mol Genet. 2011. PMID: 21750112 Free PMC article.
750 results