Nishio H - Search Results

1

Minimal residual disease monitoring in neuroblastoma patients based on the expression of a set of real-time RT-PCR markers in tumor-initiating cells.

Hartomo TB, Kozaki A, Hasegawa D, Van Huyen Pham T, Yamamoto N, Saitoh A, Ishida T, Kawasaki K, Kosaka Y, Ohashi H, Yamamoto T, Morikawa S, Hirase S, Kubokawa I, Mori T, Yanai T, Hayakawa A, Takeshima Y, Iijima K, Matsuo M, Nishio H, Nishimura N. Hartomo TB, et al. Among authors: nishio h. Oncol Rep. 2013 Apr;29(4):1629-36. doi: 10.3892/or.2013.2286. Epub 2013 Feb 12. Oncol Rep. 2013. PMID: 23417100

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

Mutation in alpha 5(IV) collagen chain gene in nonfamilial hematuria.

Kitagawa K, Nakanishi K, Iijima K, Nishio H, Sado Y, Sano K, Nakamura H, Yoshikawa N. Kitagawa K, et al. Among authors: nishio h. J Am Soc Nephrol. 1995 Aug;6(2):264-8. doi: 10.1681/ASN.V62264. J Am Soc Nephrol. 1995. PMID: 7579094

4

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

5

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 …

6

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

7

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.

8

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

9

A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.

Hagiwara Y, Nishio H, Kitoh Y, Takeshima Y, Narita N, Wada H, Yokoyama M, Nakamura H, Matsuo M. Hagiwara Y, et al. Among authors: nishio h. Am J Hum Genet. 1994 Jan;54(1):53-61. Am J Hum Genet. 1994. PMID: 8279470 Free PMC article.

10

A Japanese boy with myalgia and cramps has a novel in-frame deletion of the dystrophin gene.

Ishigaki C, Patria SY, Nishio H, Yabe M, Matsuo M. Ishigaki C, et al. Among authors: nishio h. Neurology. 1996 May;46(5):1347-50. doi: 10.1212/wnl.46.5.1347. Neurology. 1996. PMID: 8628480

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