Ohe K - Search Results

1

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.

Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Li Y, Ogaki K, Ando M, Yoshino H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda T, Mizuno Y, Uchiyama Y, Ohno K, Hattori N. Funayama M, et al. Among authors: ohe k. Lancet Neurol. 2015 Mar;14(3):274-82. doi: 10.1016/S1474-4422(14)70266-2. Epub 2015 Feb 4. Lancet Neurol. 2015. PMID: 25662902

2

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.

3

HnRNP L and hnRNP LL antagonistically modulate PTB-mediated splicing suppression of CHRNA1 pre-mRNA.

Rahman MA, Masuda A, Ohe K, Ito M, Hutchinson DO, Mayeda A, Engel AG, Ohno K. Rahman MA, et al. Among authors: ohe k. Sci Rep. 2013 Oct 14;3:2931. doi: 10.1038/srep02931. Sci Rep. 2013. PMID: 24121633 Free PMC article.

4

Competitive regulation of alternative splicing and alternative polyadenylation by hnRNP H and CstF64 determines acetylcholinesterase isoforms.

Nazim M, Masuda A, Rahman MA, Nasrin F, Takeda JI, Ohe K, Ohkawara B, Ito M, Ohno K. Nazim M, et al. Among authors: ohe k. Nucleic Acids Res. 2017 Feb 17;45(3):1455-1468. doi: 10.1093/nar/gkw823. Nucleic Acids Res. 2017. PMID: 28180311 Free PMC article.

5

New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism.

Yanase T, Takayanagi R, Oba K, Nishi Y, Ohe K, Nawata H. Yanase T, et al. Among authors: ohe k. J Clin Endocrinol Metab. 1996 Feb;81(2):530-5. doi: 10.1210/jcem.81.2.8636263. J Clin Endocrinol Metab. 1996. PMID: 8636263

6

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.

7

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.

8

[Oncogenic HMGA1a protein causes sporadic Alzheimer's disease-associated aberrant splicing].

Mayeda A, Manabe T, Ohe K. Mayeda A, et al. Among authors: ohe k. Tanpakushitsu Kakusan Koso. 2009 Dec;54(16 Suppl):2245-50. Tanpakushitsu Kakusan Koso. 2009. PMID: 21089648 Review. Japanese. No abstract available.

9

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.

10

HMGA1a induces alternative splicing of estrogen receptor alpha in MCF-7 human breast cancer cells.

Ohe K, Miyajima S, Abe I, Tanaka T, Hamaguchi Y, Harada Y, Horita Y, Beppu Y, Ito F, Yamasaki T, Terai H, Mori M, Murata Y, Tanabe M, Ashida K, Kobayashi K, Enjoji M, Yanase T, Harada N, Utsumi T, Mayeda A. Ohe K, et al. J Steroid Biochem Mol Biol. 2018 Sep;182:21-26. doi: 10.1016/j.jsbmb.2018.04.007. Epub 2018 Apr 17. J Steroid Biochem Mol Biol. 2018. PMID: 29678492

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