Nishio H - Search Results

1

Rab15 expression correlates with retinoic acid-induced differentiation of neuroblastoma cells.

Nishimura N, Van Huyen Pham T, Hartomo TB, Lee MJ, Hasegawa D, Takeda H, Kawasaki K, Kosaka Y, Yamamoto T, Morikawa S, Yamamoto N, Kubokawa I, Mori T, Yanai T, Hayakawa A, Takeshima Y, Nishio H, Matsuo M. Nishimura N, et al. Among authors: nishio h. Oncol Rep. 2011 Jul;26(1):145-51. doi: 10.3892/or.2011.1255. Epub 2011 Apr 12. Oncol Rep. 2011. PMID: 21491086

2

Partial deletion of a dystrophin gene leads to exon skipping and to loss of an intra-exon hairpin structure from the predicted mRNA precursor.

Matsuo M, Nishio H, Kitoh Y, Francke U, Nakamura H. Matsuo M, et al. Among authors: nishio h. Biochem Biophys Res Commun. 1992 Jan 31;182(2):495-500. doi: 10.1016/0006-291x(92)91759-j. Biochem Biophys Res Commun. 1992. PMID: 1734864

3

Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.

Matsuo M, Masumura T, Nishio H, Nakajima T, Kitoh Y, Takumi T, Koga J, Nakamura H. Matsuo M, et al. Among authors: nishio h. J Clin Invest. 1991 Jun;87(6):2127-31. doi: 10.1172/JCI115244. J Clin Invest. 1991. PMID: 2040695 Free PMC article.

4

Glucose, free fatty acid and ketone body metabolism in Duchenne muscular dystrophy.

Nishio H, Wada H, Matsuo T, Horikawa H, Takahashi K, Nakajima T, Matsuo M, Nakamura H. Nishio H, et al. Brain Dev. 1990;12(4):390-402. doi: 10.1016/s0387-7604(12)80071-4. Brain Dev. 1990. PMID: 2240459

5

A very small frame-shifting deletion within exon 19 of the Duchenne muscular dystrophy gene.

Matsuo M, Masumura T, Nakajima T, Kitoh Y, Takumi T, Nishio H, Koga J, Nakamura H. Matsuo M, et al. Among authors: nishio h. Biochem Biophys Res Commun. 1990 Jul 31;170(2):963-7. doi: 10.1016/0006-291x(90)92185-3. Biochem Biophys Res Commun. 1990. PMID: 2383276

6

Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.

Kitoh Y, Matsuo M, Nishio H, Nakamura H. Kitoh Y, et al. Among authors: nishio h. Kobe J Med Sci. 1994 Apr;40(2):39-48. Kobe J Med Sci. 1994. PMID: 7823533

7

Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe.

Takeshima Y, Nishio H, Sakamoto H, Nakamura H, Matsuo M. Takeshima Y, et al. Among authors: nishio h. J Clin Invest. 1995 Feb;95(2):515-20. doi: 10.1172/JCI117693. J Clin Invest. 1995. PMID: 7860733 Free PMC article.

Molecular analysis of dystrophin Kobe showed that exon 19 of the dystrophin gene bearing 52-bp deletion was skipped during splicing, although the known consensus sequences at the 5' and 3' splice sites of exon 19 were maintained (Matsuo, M., T. Masumura, H. Nishio, …

Molecular analysis of dystrophin Kobe showed that exon 19 of the dystrophin gene bearing 52-bp deletion was skipped during splicing, althoug …

8

Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype.

Takeshima Y, Nishio H, Narita N, Wada H, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Takeshima Y, et al. Among authors: nishio h. Neurology. 1994 Sep;44(9):1648-51. doi: 10.1212/wnl.44.9.1648. Neurology. 1994. PMID: 7936290

9

Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.

Nishio H, Takeshima Y, Narita N, Yanagawa H, Suzuki Y, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Nishio H, et al. J Clin Invest. 1994 Sep;94(3):1037-42. doi: 10.1172/JCI117417. J Clin Invest. 1994. PMID: 8083345 Free PMC article.

10

Brain- and muscle-type promoters of the dystrophin gene are selected in peripheral lymphocytes and Epstein Barr virus-transformed lymphoblastoid [correction of lymphoplastoid] cells.

Nishio H, Matsuo M, Kitoh Y, Narita N, Shimmoto M, Suzuki Y, Nakamura H. Nishio H, et al. J Neurol. 1993 Dec;241(2):81-6. doi: 10.1007/BF00869768. J Neurol. 1993. PMID: 8138829

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