Araki T - Search Results

1

Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability.

Ueki J, Nakamori M, Nakamura M, Nishikawa M, Yoshida Y, Tanaka A, Morizane A, Kamon M, Araki T, Takahashi MP, Watanabe A, Inagaki N, Sakurai H. Ueki J, et al. Among authors: araki t. Sci Rep. 2017 Feb 13;7:42522. doi: 10.1038/srep42522. Sci Rep. 2017. PMID: 28211918 Free PMC article.

2

Glutamate signals through mGluR2 to control Schwann cell differentiation and proliferation.

Saitoh F, Wakatsuki S, Tokunaga S, Fujieda H, Araki T. Saitoh F, et al. Among authors: araki t. Sci Rep. 2016 Jul 19;6:29856. doi: 10.1038/srep29856. Sci Rep. 2016. PMID: 27432639 Free PMC article.

3

Taxanes and platinum derivatives impair Schwann cells via distinct mechanisms.

Imai S, Koyanagi M, Azimi Z, Nakazato Y, Matsumoto M, Ogihara T, Yonezawa A, Omura T, Nakagawa S, Wakatsuki S, Araki T, Kaneko S, Nakagawa T, Matsubara K. Imai S, et al. Among authors: araki t. Sci Rep. 2017 Jul 20;7(1):5947. doi: 10.1038/s41598-017-05784-1. Sci Rep. 2017. PMID: 28729624 Free PMC article.

4

Genetic inhibition of CRMP2 phosphorylation at serine 522 promotes axonal regeneration after optic nerve injury.

Kondo S, Takahashi K, Kinoshita Y, Nagai J, Wakatsuki S, Araki T, Goshima Y, Ohshima T. Kondo S, et al. Among authors: araki t. Sci Rep. 2019 May 10;9(1):7188. doi: 10.1038/s41598-019-43658-w. Sci Rep. 2019. PMID: 31076621 Free PMC article.

5

Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells.

Huang K, Masuda A, Chen G, Bushra S, Kamon M, Araki T, Kinoshita M, Ohkawara B, Ito M, Ohno K. Huang K, et al. Among authors: araki t. Sci Rep. 2020 Feb 13;10(1):2558. doi: 10.1038/s41598-020-59517-y. Sci Rep. 2020. PMID: 32054946 Free PMC article.

6

Generation of a transgene-free iPSC line and genetically modified line from a facioscapulohumeral muscular dystrophy type 2 (FSHD2) patient with SMCHD1 p.Lys607Ter mutation.

Sasaki-Honda M, Kagita A, Jonouchi T, Araki T, Hotta A, Sakurai H. Sasaki-Honda M, et al. Among authors: araki t. Stem Cell Res. 2020 Jun 24;47:101884. doi: 10.1016/j.scr.2020.101884. Online ahead of print. Stem Cell Res. 2020. PMID: 32711388 Free article.

7

Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1.

Nakamori M, Shimizu H, Ogawa K, Hasuike Y, Nakajima T, Sakurai H, Araki T, Okada Y, Kakita A, Mochizuki H. Nakamori M, et al. Among authors: araki t. Brain Commun. 2022 Jun 10;4(3):fcac154. doi: 10.1093/braincomms/fcac154. eCollection 2022. Brain Commun. 2022. PMID: 35770133 Free PMC article.

8

A mutation in DOK7 in congenital myasthenic syndrome forms aggresome in cultured cells, and reduces DOK7 expression and MuSK phosphorylation in patient-derived iPS cells.

Zhang S, Ohkawara B, Ito M, Huang Z, Zhao F, Nakata T, Takeuchi T, Sakurai H, Komaki H, Kamon M, Araki T, Ohno K. Zhang S, et al. Among authors: araki t. Hum Mol Genet. 2023 Apr 20;32(9):1511-1523. doi: 10.1093/hmg/ddac306. Hum Mol Genet. 2023. PMID: 36579833 Free PMC article.

9

Identification of ZNF850 as a novel CTG repeat expansion-related gene in myotonic dystrophy type 1 patient-derived iPSCs.

Kamon M, Wakatsuki S, Nakamori M, Takahashi MP, Mori-Yoshimura M, Komaki H, Araki T. Kamon M, et al. Among authors: araki t. Hum Mol Genet. 2024 Dec 16:ddae186. doi: 10.1093/hmg/ddae186. Online ahead of print. Hum Mol Genet. 2024. PMID: 39679849

10

Critical role of CRAG, a splicing variant of centaurin-γ3/AGAP3, in ELK1-dependent SRF activation at PML bodies.

Nagashima S, Takeda K, Shiiba I, Higashi M, Fukuda T, Tokuyama T, Matsushita N, Nagano S, Araki T, Kaneko M, Shioi G, Inatome R, Yanagi S. Nagashima S, et al. Among authors: araki t. Sci Rep. 2019 Dec 27;9(1):20107. doi: 10.1038/s41598-019-56559-9. Sci Rep. 2019. PMID: 31882856 Free PMC article.

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