Hirose S - Search Results

1

Developmental changes in brain activity of heterozygous Scn1a knockout rats.

Tahara M, Higurashi N, Hata J, Nishikawa M, Ito K, Hirose S, Kaneko T, Mashimo T, Sakuma T, Yamamoto T, Okano HJ. Tahara M, et al. Among authors: hirose s. Front Neurol. 2023 Mar 14;14:1125089. doi: 10.3389/fneur.2023.1125089. eCollection 2023. Front Neurol. 2023. PMID: 36998780 Free PMC article.

2

Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene.

Tanaka Y, Sone T, Higurashi N, Sakuma T, Suzuki S, Ishikawa M, Yamamoto T, Mitsui J, Tsuji H, Okano H, Hirose S. Tanaka Y, et al. Among authors: hirose s. Stem Cell Res. 2018 Apr;28:100-104. doi: 10.1016/j.scr.2018.01.036. Epub 2018 Feb 2. Stem Cell Res. 2018. PMID: 29453127 Free article.

3

On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation.

Shi X, Wang J, Kurahashi H, Ishii A, Higurashi N, Kaneko S, Hirose S. Shi X, et al. Among authors: hirose s. Brain Dev. 2012 Sep;34(8):617-9. doi: 10.1016/j.braindev.2011.11.005. Epub 2011 Dec 27. Brain Dev. 2012. PMID: 22206733

4

Establishment of a human induced stem cell line (FUi002-A) from Dravet syndrome patient carrying heterozygous R1525X mutation in SCN1A gene.

Tanaka Y, Higurashi N, Shirasu N, Yasunaga S, Moreira KM, Okano H, Hirose S. Tanaka Y, et al. Among authors: hirose s. Stem Cell Res. 2018 Aug;31:11-15. doi: 10.1016/j.scr.2018.06.008. Epub 2018 Jun 19. Stem Cell Res. 2018. PMID: 29981888 Free article.

5

Genetics and gene therapy in Dravet syndrome.

Higurashi N, Broccoli V, Hirose S. Higurashi N, et al. Among authors: hirose s. Epilepsy Behav. 2022 Jun;131(Pt B):108043. doi: 10.1016/j.yebeh.2021.108043. Epub 2021 May 28. Epilepsy Behav. 2022. PMID: 34053869 Review.

6

Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.

Wang JW, Shi XY, Kurahashi H, Hwang SK, Ishii A, Higurashi N, Kaneko S, Hirose S; Epilepsy Genetic Study Group Japan. Wang JW, et al. Among authors: hirose s. Epilepsy Res. 2012 Dec;102(3):195-200. doi: 10.1016/j.eplepsyres.2012.06.006. Epub 2012 Jul 20. Epilepsy Res. 2012. PMID: 23195492

7

Establishment of human induced pluripotent stem cells derived from skin cells of a patient with Dravet syndrome.

Kimura Y, Tanaka Y, Shirasu N, Yasunaga S, Higurashi N, Hirose S. Kimura Y, et al. Among authors: hirose s. Stem Cell Res. 2020 Jun 15;47:101857. doi: 10.1016/j.scr.2020.101857. Online ahead of print. Stem Cell Res. 2020. PMID: 32599563 Free article.

8

PCDH19 mutation in Japanese females with epilepsy.

Higurashi N, Shi X, Yasumoto S, Oguni H, Sakauchi M, Itomi K, Miyamoto A, Shiraishi H, Kato T, Makita Y, Hirose S. Higurashi N, et al. Among authors: hirose s. Epilepsy Res. 2012 Mar;99(1-2):28-37. doi: 10.1016/j.eplepsyres.2011.10.014. Epub 2011 Nov 1. Epilepsy Res. 2012. PMID: 22050978

9

A human Dravet syndrome model from patient induced pluripotent stem cells.

Higurashi N, Uchida T, Lossin C, Misumi Y, Okada Y, Akamatsu W, Imaizumi Y, Zhang B, Nabeshima K, Mori MX, Katsurabayashi S, Shirasaka Y, Okano H, Hirose S. Higurashi N, et al. Among authors: hirose s. Mol Brain. 2013 May 2;6:19. doi: 10.1186/1756-6606-6-19. Mol Brain. 2013. PMID: 23639079 Free PMC article.

10

Application of induced pluripotent stem cells in epilepsy.

Hirose S, Tanaka Y, Shibata M, Kimura Y, Ishikawa M, Higurashi N, Yamamoto T, Ichise E, Chiyonobu T, Ishii A. Hirose S, et al. Mol Cell Neurosci. 2020 Oct;108:103535. doi: 10.1016/j.mcn.2020.103535. Epub 2020 Aug 4. Mol Cell Neurosci. 2020. PMID: 32758699 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

2,057 results

Search Page