Ohsawa R - Search Results

1

Roles of bHLH genes in neural stem cell differentiation.

Kageyama R, Ohtsuka T, Hatakeyama J, Ohsawa R. Kageyama R, et al. Among authors: ohsawa r. Exp Cell Res. 2005 Jun 10;306(2):343-8. doi: 10.1016/j.yexcr.2005.03.015. Epub 2005 Apr 13. Exp Cell Res. 2005. PMID: 15925590 Review.

2

Mash1 and Math3 are required for development of branchiomotor neurons and maintenance of neural progenitors.

Ohsawa R, Ohtsuka T, Kageyama R. Ohsawa R, et al. J Neurosci. 2005 Jun 22;25(25):5857-65. doi: 10.1523/JNEUROSCI.4621-04.2005. J Neurosci. 2005. PMID: 15976074 Free PMC article.

3

Hes1 and Hes5 control the progenitor pool, intermediate lobe specification, and posterior lobe formation in the pituitary development.

Kita A, Imayoshi I, Hojo M, Kitagawa M, Kokubu H, Ohsawa R, Ohtsuka T, Kageyama R, Hashimoto N. Kita A, et al. Among authors: ohsawa r. Mol Endocrinol. 2007 Jun;21(6):1458-66. doi: 10.1210/me.2007-0039. Epub 2007 Apr 10. Mol Endocrinol. 2007. PMID: 17426285

4

Regulation of retinal cell fate specification by multiple transcription factors.

Ohsawa R, Kageyama R. Ohsawa R, et al. Brain Res. 2008 Feb 4;1192:90-8. doi: 10.1016/j.brainres.2007.04.014. Epub 2007 Apr 11. Brain Res. 2008. PMID: 17488643 Review.

5

Sustained Notch signaling in progenitors is required for sequential emergence of distinct cell lineages during organogenesis.

Zhu X, Zhang J, Tollkuhn J, Ohsawa R, Bresnick EH, Guillemot F, Kageyama R, Rosenfeld MG. Zhu X, et al. Among authors: ohsawa r. Genes Dev. 2006 Oct 1;20(19):2739-53. doi: 10.1101/gad.1444706. Genes Dev. 2006. PMID: 17015435 Free PMC article.

6

A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia.

Morino H, Matsuda Y, Muguruma K, Miyamoto R, Ohsawa R, Ohtake T, Otobe R, Watanabe M, Maruyama H, Hashimoto K, Kawakami H. Morino H, et al. Among authors: ohsawa r. Mol Brain. 2015 Dec 29;8:89. doi: 10.1186/s13041-015-0180-4. Mol Brain. 2015. PMID: 26715324 Free PMC article.

7

Optineurin regulates osteoblastogenesis through STAT1.

Mizuno N, Iwata T, Ohsawa R, Ouhara K, Matsuda S, Kajiya M, Matsuda Y, Kume K, Tada Y, Morino H, Yoshimoto T, Ueki Y, Mihara K, Sotomaru Y, Takeda K, Munenaga S, Fujita T, Kawaguchi H, Shiba H, Kawakami H, Kurihara H. Mizuno N, et al. Among authors: ohsawa r. Biochem Biophys Res Commun. 2020 May 14;525(4):889-894. doi: 10.1016/j.bbrc.2020.03.028. Epub 2020 Mar 12. Biochem Biophys Res Commun. 2020. PMID: 32171527

8

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.

Tada Y, Kume K, Matsuda Y, Kurashige T, Kanaya Y, Ohsawa R, Morino H, Tabu H, Kaneko S, Suenaga T, Kakizuka A, Kawakami H. Tada Y, et al. Among authors: ohsawa r. J Hum Genet. 2020 Apr;65(4):363-369. doi: 10.1038/s10038-019-0717-y. Epub 2020 Jan 7. J Hum Genet. 2020. PMID: 31907387 Clinical Trial.

9

Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia.

Matsuda Y, Morino H, Miyamoto R, Kurashige T, Kume K, Mizuno N, Kanaya Y, Tada Y, Ohsawa R, Yokota K, Shimozawa N, Maruyama H, Kawakami H. Matsuda Y, et al. Among authors: ohsawa r. Neurol Genet. 2020 Jan 16;6(1):e396. doi: 10.1212/NXG.0000000000000396. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042923 Free PMC article.

10

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.

Kume K, Morino H, Miyamoto R, Matsuda Y, Ohsawa R, Kanaya Y, Tada Y, Kurashige T, Kawakami H. Kume K, et al. Among authors: ohsawa r. BMC Med Genet. 2020 Mar 31;21(1):68. doi: 10.1186/s12881-020-01002-4. BMC Med Genet. 2020. PMID: 32234020 Free PMC article.

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