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Reduced astrocytic reactivity in human brains and midbrain organoids with PRKN mutations.
Kano M, Takanashi M, Oyama G, Yoritaka A, Hatano T, Shiba-Fukushima K, Nagai M, Nishiyama K, Hasegawa K, Inoshita T, Ishikawa KI, Akamatsu W, Imai Y, Bolognin S, Schwamborn JC, Hattori N. Kano M, et al. Among authors: takanashi m. NPJ Parkinsons Dis. 2020 Nov 13;6(1):33. doi: 10.1038/s41531-020-00137-8. NPJ Parkinsons Dis. 2020. PMID: 33298969 Free PMC article.
Expanding the clinical phenotype of SNCA duplication carriers.
Nishioka K, Ross OA, Ishii K, Kachergus JM, Ishiwata K, Kitagawa M, Kono S, Obi T, Mizoguchi K, Inoue Y, Imai H, Takanashi M, Mizuno Y, Farrer MJ, Hattori N. Nishioka K, et al. Among authors: takanashi m. Mov Disord. 2009 Sep 15;24(12):1811-9. doi: 10.1002/mds.22682. Mov Disord. 2009. PMID: 19562770
The effect of Ndrg2 expression on astroglial activation.
Takeichi T, Takarada-Iemata M, Hashida K, Sudo H, Okuda T, Kokame K, Hatano T, Takanashi M, Funabe S, Hattori N, Kitamura O, Kitao Y, Hori O. Takeichi T, et al. Among authors: takanashi m. Neurochem Int. 2011 Aug;59(1):21-7. doi: 10.1016/j.neuint.2011.03.019. Epub 2011 Jun 13. Neurochem Int. 2011. PMID: 21672576
[Neurodegenerative diseases].
Takanashi M, Hattori N. Takanashi M, et al. Nihon Rinsho. 2012 Jan;70(1):94-8. Nihon Rinsho. 2012. PMID: 22413500 Review. Japanese.
Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS.
Ogaki K, Li Y, Takanashi M, Ishikawa K, Kobayashi T, Nonaka T, Hasegawa M, Kishi M, Yoshino H, Funayama M, Tsukamoto T, Shioya K, Yokochi M, Imai H, Sasaki R, Kokubo Y, Kuzuhara S, Motoi Y, Tomiyama H, Hattori N. Ogaki K, et al. Among authors: takanashi m. Parkinsonism Relat Disord. 2013 Jan;19(1):15-20. doi: 10.1016/j.parkreldis.2012.06.019. Epub 2012 Jul 18. Parkinsonism Relat Disord. 2013. PMID: 22818528
412 results