Ohe K - Search Results

1

Rectifier of aberrant mRNA splicing recovers tRNA modification in familial dysautonomia.

Yoshida M, Kataoka N, Miyauchi K, Ohe K, Iida K, Yoshida S, Nojima T, Okuno Y, Onogi H, Usui T, Takeuchi A, Hosoya T, Suzuki T, Hagiwara M. Yoshida M, et al. Among authors: ohe k. Proc Natl Acad Sci U S A. 2015 Mar 3;112(9):2764-9. doi: 10.1073/pnas.1415525112. Epub 2015 Feb 9. Proc Natl Acad Sci U S A. 2015. PMID: 25675486 Free PMC article.

2

RBM24 promotes U1 snRNP recognition of the mutated 5' splice site in the IKBKAP gene of familial dysautonomia.

Ohe K, Yoshida M, Nakano-Kobayashi A, Hosokawa M, Sako Y, Sakuma M, Okuno Y, Usui T, Ninomiya K, Nojima T, Kataoka N, Hagiwara M. Ohe K, et al. RNA. 2017 Sep;23(9):1393-1403. doi: 10.1261/rna.059428.116. Epub 2017 Jun 7. RNA. 2017. PMID: 28592461 Free PMC article.

3

Development of an orally available inhibitor of CLK1 for skipping a mutated dystrophin exon in Duchenne muscular dystrophy.

Sako Y, Ninomiya K, Okuno Y, Toyomoto M, Nishida A, Koike Y, Ohe K, Kii I, Yoshida S, Hashimoto N, Hosoya T, Matsuo M, Hagiwara M. Sako Y, et al. Among authors: ohe k. Sci Rep. 2017 May 30;7:46126. doi: 10.1038/srep46126. Sci Rep. 2017. PMID: 28555643 Free PMC article.

4

Modulation of alternative splicing with chemical compounds in new therapeutics for human diseases.

Ohe K, Hagiwara M. Ohe K, et al. ACS Chem Biol. 2015 Apr 17;10(4):914-24. doi: 10.1021/cb500697f. Epub 2015 Jan 20. ACS Chem Biol. 2015. PMID: 25560473 Review.

5

A direct role of SRY and SOX proteins in pre-mRNA splicing.

Ohe K, Lalli E, Sassone-Corsi P. Ohe K, et al. Proc Natl Acad Sci U S A. 2002 Feb 5;99(3):1146-51. doi: 10.1073/pnas.022645899. Epub 2002 Jan 29. Proc Natl Acad Sci U S A. 2002. PMID: 11818535 Free PMC article.

6

HnRNP C, YB-1 and hnRNP L coordinately enhance skipping of human MUSK exon 10 to generate a Wnt-insensitive MuSK isoform.

Nasrin F, Rahman MA, Masuda A, Ohe K, Takeda J, Ohno K. Nasrin F, et al. Among authors: ohe k. Sci Rep. 2014 Oct 30;4:6841. doi: 10.1038/srep06841. Sci Rep. 2014. PMID: 25354590 Free PMC article.

7

HMGA1a is involved in specific splice site regulation of human immunodeficiency virus type 1.

Tsuruno C, Ohe K, Kuramitsu M, Kohma T, Takahama Y, Hamaguchi Y, Hamaguchi I, Okuma K. Tsuruno C, et al. Among authors: ohe k. Biochem Biophys Res Commun. 2011 Mar 25;406(4):512-7. doi: 10.1016/j.bbrc.2011.02.059. Epub 2011 Feb 15. Biochem Biophys Res Commun. 2011. PMID: 21329653

8

HMGA1a: sequence-specific RNA-binding factor causing sporadic Alzheimer's disease-linked exon skipping of presenilin-2 pre-mRNA.

Manabe T, Ohe K, Katayama T, Matsuzaki S, Yanagita T, Okuda H, Bando Y, Imaizumi K, Reeves R, Tohyama M, Mayeda A. Manabe T, et al. Among authors: ohe k. Genes Cells. 2007 Oct;12(10):1179-91. doi: 10.1111/j.1365-2443.2007.01123.x. Genes Cells. 2007. PMID: 17903177 Free article.

9

HMGA1a trapping of U1 snRNP at an authentic 5' splice site induces aberrant exon skipping in sporadic Alzheimer's disease.

Ohe K, Mayeda A. Ohe K, et al. Mol Cell Biol. 2010 May;30(9):2220-8. doi: 10.1128/MCB.00114-10. Epub 2010 Mar 1. Mol Cell Biol. 2010. PMID: 20194618 Free PMC article.

10

Nested introns in an intron: evidence of multi-step splicing in a large intron of the human dystrophin pre-mRNA.

Suzuki H, Kameyama T, Ohe K, Tsukahara T, Mayeda A. Suzuki H, et al. Among authors: ohe k. FEBS Lett. 2013 Mar 18;587(6):555-61. doi: 10.1016/j.febslet.2013.01.057. Epub 2013 Feb 5. FEBS Lett. 2013. PMID: 23395799 Free article.

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