Sakai N - Search Results

1

Comparison of two families with and without ataxia harboring novel variants in PRKCG.

Tada Y, Kume K, Noguchi S, Sekiya T, Nishinaka K, Ishiguchi H, Koh J, Emori S, Nakayama Y, Kurashige T, Izumi Y, Ito H, Sakai N, Kawakami H. Tada Y, et al. Among authors: sakai n. J Hum Genet. 2022 Oct;67(10):595-599. doi: 10.1038/s10038-022-01057-6. Epub 2022 Jun 28. J Hum Genet. 2022. PMID: 35760954

2

Correction: Comparison of two families with and without ataxia harboring novel variants in PRKCG.

Tada Y, Kume K, Noguchi S, Sekiya T, Nishinaka K, Ishiguchi H, Koh J, Emori S, Nakayama Y, Kurashige T, Izumi Y, Ito H, Sakai N, Kawakami H. Tada Y, et al. Among authors: sakai n. J Hum Genet. 2022 Oct;67(10):621. doi: 10.1038/s10038-022-01064-7. J Hum Genet. 2022. PMID: 35794208 No abstract available.

3

Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.

Hiramoto K, Kawakami H, Inoue K, Seki T, Maruyama H, Morino H, Matsumoto M, Kurisu K, Sakai N. Hiramoto K, et al. Among authors: sakai n. Mov Disord. 2006 Sep;21(9):1355-60. doi: 10.1002/mds.20970. Mov Disord. 2006. PMID: 16763984

4

Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death.

Seki T, Adachi N, Ono Y, Mochizuki H, Hiramoto K, Amano T, Matsubayashi H, Matsumoto M, Kawakami H, Saito N, Sakai N. Seki T, et al. Among authors: sakai n. J Biol Chem. 2005 Aug 12;280(32):29096-106. doi: 10.1074/jbc.M501716200. Epub 2005 Jun 17. J Biol Chem. 2005. PMID: 15964845 Free article.

5

Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein.

Takahashi H, Adachi N, Shirafuji T, Danno S, Ueyama T, Vendruscolo M, Shuvaev AN, Sugimoto T, Seki T, Hamada D, Irie K, Hirai H, Sakai N, Saito N. Takahashi H, et al. Among authors: sakai n. Hum Mol Genet. 2015 Jan 15;24(2):525-39. doi: 10.1093/hmg/ddu472. Epub 2014 Sep 12. Hum Mol Genet. 2015. PMID: 25217572

6

Spinocerebellar ataxia type 14 caused by a nonsense mutation in the PRKCG gene.

Shirafuji T, Shimazaki H, Miyagi T, Ueyama T, Adachi N, Tanaka S, Hide I, Saito N, Sakai N. Shirafuji T, et al. Among authors: sakai n. Mol Cell Neurosci. 2019 Jul;98:46-53. doi: 10.1016/j.mcn.2019.05.005. Epub 2019 May 31. Mol Cell Neurosci. 2019. PMID: 31158466

7

Characterization of intracellular calcium mobilization induced by remimazolam, a newly approved intravenous anesthetic.

Urabe T, Miyoshi H, Narasaki S, Yanase Y, Uchida K, Noguchi S, Hide M, Tsutsumi YM, Sakai N. Urabe T, et al. Among authors: sakai n. PLoS One. 2022 Feb 1;17(2):e0263395. doi: 10.1371/journal.pone.0263395. eCollection 2022. PLoS One. 2022. PMID: 35104283 Free PMC article.

8

Elucidation of the molecular mechanism and exploration of novel therapeutics for spinocerebellar ataxia caused by mutant protein kinase Cγ.

Seki T, Adachi N, Abe-Seki N, Shimahara T, Takahashi H, Yamamoto K, Saito N, Sakai N. Seki T, et al. Among authors: sakai n. J Pharmacol Sci. 2011;116(3):239-47. doi: 10.1254/jphs.11r04cp. Epub 2011 Jun 10. J Pharmacol Sci. 2011. PMID: 21666345 Free article. Review.

9

Mutant γPKC that causes spinocerebellar ataxia type 14 upregulates Hsp70, which protects cells from the mutant's cytotoxicity.

Ogawa K, Seki T, Onji T, Adachi N, Tanaka S, Hide I, Saito N, Sakai N. Ogawa K, et al. Among authors: sakai n. Biochem Biophys Res Commun. 2013 Oct 11;440(1):25-30. doi: 10.1016/j.bbrc.2013.09.013. Epub 2013 Sep 8. Biochem Biophys Res Commun. 2013. PMID: 24021284

10

Mutant gammaPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells.

Seki T, Shimahara T, Yamamoto K, Abe N, Amano T, Adachi N, Takahashi H, Kashiwagi K, Saito N, Sakai N. Seki T, et al. Among authors: sakai n. Neurobiol Dis. 2009 Feb;33(2):260-73. doi: 10.1016/j.nbd.2008.10.013. Epub 2008 Nov 8. Neurobiol Dis. 2009. PMID: 19041943

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