Araki T - Search Results

1

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.

2

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.

3

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.

4

TDP-43 transports ribosomal protein mRNA to regulate axonal local translation in neuronal axons.

Nagano S, Jinno J, Abdelhamid RF, Jin Y, Shibata M, Watanabe S, Hirokawa S, Nishizawa M, Sakimura K, Onodera O, Okada H, Okada T, Saito Y, Takahashi-Fujigasaki J, Murayama S, Wakatsuki S, Mochizuki H, Araki T. Nagano S, et al. Among authors: araki t. Acta Neuropathol. 2020 Nov;140(5):695-713. doi: 10.1007/s00401-020-02205-y. Epub 2020 Aug 16. Acta Neuropathol. 2020. PMID: 32803350

5

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.

6

Regulation of neuronal/axonal degeneration by ZNRF1 ubiquitin ligase.

Araki T, Wakatsuki S. Araki T, et al. Neurosci Res. 2019 Feb;139:21-25. doi: 10.1016/j.neures.2018.07.008. Epub 2018 Aug 15. Neurosci Res. 2019. PMID: 30118738 Review.

7

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.

8

Axonal Transport and Local Translation of mRNA in Neurodegenerative Diseases.

Nagano S, Araki T. Nagano S, et al. Among authors: araki t. Front Mol Neurosci. 2021 Jun 14;14:697973. doi: 10.3389/fnmol.2021.697973. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34194300 Free PMC article. Review.

9

Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3.

Tateno M, Kato S, Sakurai T, Nukina N, Takahashi R, Araki T. Tateno M, et al. Among authors: araki t. Hum Mol Genet. 2009 Mar 1;18(5):942-55. doi: 10.1093/hmg/ddn422. Epub 2008 Dec 16. Hum Mol Genet. 2009. PMID: 19088126 Free PMC article.

10

Wallerian degeneration slow mouse neurons are protected against cell death caused by mechanisms involving mitochondrial electron transport dysfunction.

Tokunaga S, Araki T. Tokunaga S, et al. Among authors: araki t. J Neurosci Res. 2012 Mar;90(3):664-71. doi: 10.1002/jnr.22792. Epub 2011 Dec 20. J Neurosci Res. 2012. PMID: 22183770

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