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Proteolytic ectodomain shedding of muscle-specific tyrosine kinase in myasthenia gravis.
Mori S, Suzuki S, Konishi T, Kawaguchi N, Kishi M, Kuwabara S, Ishizuchi K, Zhou H, Shibasaki F, Tsumoto H, Omura T, Miura Y, Mori S, Higashihara M, Murayama S, Shigemoto K. Mori S, et al. Exp Neurol. 2023 Mar;361:114300. doi: 10.1016/j.expneurol.2022.114300. Epub 2022 Dec 13. Exp Neurol. 2023. PMID: 36525997 Free article.
Association of the formiminotransferase N-terminal sub-domain containing gene and thrombospondin, type 1, domain-containing 7A gene with the prevalence of vertebral fracture in 2427 consecutive autopsy cases.
Zhou H, Mori S, Kou I, Fuku N, Naka Mieno M, Honma N, Arai T, Sawabe M, Tanaka M, Ikegawa S, Ito H. Zhou H, et al. Among authors: mori s. J Hum Genet. 2013 Feb;58(2):109-12. doi: 10.1038/jhg.2012.145. Epub 2013 Jan 10. J Hum Genet. 2013. PMID: 23303384
A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population.
Zhou H, Mori S, Tanaka M, Sawabe M, Arai T, Muramatsu M, Mieno MN, Shinkai S, Yamada Y, Miyachi M, Murakami H, Sanada K, Ito H. Zhou H, et al. Among authors: mori s. J Bone Miner Metab. 2015 Nov;33(6):694-700. doi: 10.1007/s00774-014-0636-0. Epub 2015 Jan 31. J Bone Miner Metab. 2015. PMID: 25637295
Genetic risk score based on the prevalence of vertebral fracture in Japanese women with osteoporosis.
Zhou H, Mori S, Ishizaki T, Takahashi A, Matsuda K, Koretsune Y, Minami S, Higashiyama M, Imai S, Yoshimori K, Doita M, Yamada A, Nagayama S, Kaneko K, Asai S, Shiono M, Kubo M, Ito H. Zhou H, et al. Among authors: mori s. Bone Rep. 2016 Jul 12;5:168-172. doi: 10.1016/j.bonr.2016.07.001. eCollection 2016 Dec. Bone Rep. 2016. PMID: 28580384 Free PMC article.
5,249 results