Koebis M - Search Results

1

Ishiura S, Oana K, Koebis M. Ishiura S, et al. Among authors: koebis m. Rinsho Shinkeigaku. 2013;53(11):1109-11. doi: 10.5692/clinicalneurol.53.1109. Rinsho Shinkeigaku. 2013. PMID: 24291894 Review. Japanese.

2

Alternative splicing of PDLIM3/ALP, for α-actinin-associated LIM protein 3, is aberrant in persons with myotonic dystrophy.

Ohsawa N, Koebis M, Suo S, Nishino I, Ishiura S. Ohsawa N, et al. Among authors: koebis m. Biochem Biophys Res Commun. 2011 May 27;409(1):64-9. doi: 10.1016/j.bbrc.2011.04.106. Epub 2011 Apr 28. Biochem Biophys Res Commun. 2011. PMID: 21549096

3

Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1.

Koebis M, Ohsawa N, Kino Y, Sasagawa N, Nishino I, Ishiura S. Koebis M, et al. Genes Cells. 2011 Sep;16(9):961-72. doi: 10.1111/j.1365-2443.2011.01542.x. Epub 2011 Jul 28. Genes Cells. 2011. PMID: 21794030 Free article.

4

Regulation of the alternative splicing of sarcoplasmic reticulum Ca²⁺-ATPase1 (SERCA1) by phorbol 12-myristate 13-acetate (PMA) via a PKC pathway.

Zhao Y, Koebis M, Suo S, Ohno S, Ishiura S. Zhao Y, et al. Among authors: koebis m. Biochem Biophys Res Commun. 2012 Jun 29;423(2):212-7. doi: 10.1016/j.bbrc.2012.05.033. Epub 2012 May 15. Biochem Biophys Res Commun. 2012. PMID: 22609207

5

Ultrasound-enhanced delivery of morpholino with Bubble liposomes ameliorates the myotonia of myotonic dystrophy model mice.

Koebis M, Kiyatake T, Yamaura H, Nagano K, Higashihara M, Sonoo M, Hayashi Y, Negishi Y, Endo-Takahashi Y, Yanagihara D, Matsuda R, Takahashi MP, Nishino I, Ishiura S. Koebis M, et al. Sci Rep. 2013;3:2242. doi: 10.1038/srep02242. Sci Rep. 2013. PMID: 23873129 Free PMC article.

6

A high-salinity solution with calcium chloride enables RNase-free, easy plasmid isolation within 55 minutes.

Sasagawa N, Koebis M, Yonemura Y, Mitsuhashi H, Ishiura S. Sasagawa N, et al. Among authors: koebis m. Biosci Trends. 2013 Dec;7(6):270-5. Biosci Trends. 2013. PMID: 24390365 Free article.

7

ABLIM1 splicing is abnormal in skeletal muscle of patients with DM1 and regulated by MBNL, CELF and PTBP1.

Ohsawa N, Koebis M, Mitsuhashi H, Nishino I, Ishiura S. Ohsawa N, et al. Among authors: koebis m. Genes Cells. 2015 Feb;20(2):121-34. doi: 10.1111/gtc.12201. Epub 2014 Nov 18. Genes Cells. 2015. PMID: 25403273 Free article.

8

Splicing of human chloride channel 1.

Nakamura T, Ohsawa-Yoshida N, Zhao Y, Koebis M, Oana K, Mitsuhashi H, Ishiura S. Nakamura T, et al. Among authors: koebis m. Biochem Biophys Rep. 2015 Nov 11;5:63-69. doi: 10.1016/j.bbrep.2015.11.006. eCollection 2016 Mar. Biochem Biophys Rep. 2015. PMID: 28955807 Free PMC article.

9

Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus.

Saito R, Koebis M, Nagai T, Shimizu K, Liao J, Wulaer B, Sugaya Y, Nagahama K, Uesaka N, Kushima I, Mori D, Maruyama K, Nakao K, Kurihara H, Yamada K, Kano M, Fukada Y, Ozaki N, Aiba A. Saito R, et al. Among authors: koebis m. Transl Psychiatry. 2020 Feb 5;10(1):35. doi: 10.1038/s41398-020-0723-z. Transl Psychiatry. 2020. PMID: 32066675 Free PMC article.

10

Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders.

Saito R, Miyoshi C, Koebis M, Kushima I, Nakao K, Mori D, Ozaki N, Funato H, Yanagisawa M, Aiba A. Saito R, et al. Among authors: koebis m. Mol Brain. 2021 Apr 12;14(1):68. doi: 10.1186/s13041-021-00778-7. Mol Brain. 2021. PMID: 33845872 Free PMC article.

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