Miyashita A - Search Results

1

Sample-size properties of a case-control association analysis of multistage SNP studies for identifying disease susceptibility genes.

Kitamura N, Akazawa K, Toyabe SI, Miyashita A, Kuwano R, Nakamura J. Kitamura N, et al. Among authors: miyashita a. J Hum Genet. 2008;53(5):390-400. doi: 10.1007/s10038-008-0258-2. Epub 2008 Feb 21. J Hum Genet. 2008. PMID: 18288444

2

A gene trap strategy for identifying the gene expressed in the embryonic nervous system.

Shirai M, Miyashita A, Ishii N, Itoh Y, Satokata I, Watanabe YG, Kuwano R. Shirai M, et al. Among authors: miyashita a. Zoolog Sci. 1996 Apr;13(2):277-83. doi: 10.2108/zsj.13.277. Zoolog Sci. 1996. PMID: 8766926

3

Molecular cloning of a novel 130-kDa cytoplasmic protein, Ankhzn, containing Ankyrin repeats hooked to a zinc finger motif.

Ito K, Ishii N, Miyashita A, Tominaga K, Kuriyama H, Maruyama H, Shirai M, Naito M, Arakawa M, Kuwano R. Ito K, et al. Among authors: miyashita a. Biochem Biophys Res Commun. 1999 Apr 2;257(1):206-13. doi: 10.1006/bbrc.1999.0430. Biochem Biophys Res Commun. 1999. PMID: 10092534

4

Five different genes, Eif4a1, Cd68, Supl15h, Sox15 and Fxr2h, are clustered in a 40 kb region of mouse chromosome 11.

Miyashita A, Shimizu N, Endo N, Hanyuu T, Ishii N, Ito K, Itoh Y, Shirai M, Nakajima T, Odani S, Kuwano R. Miyashita A, et al. Gene. 1999 Sep 3;237(1):53-60. doi: 10.1016/s0378-1119(99)00301-7. Gene. 1999. PMID: 10524236

5

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S. Hara K, et al. Among authors: miyashita a. Neurology. 2004 Feb 24;62(4):648-51. doi: 10.1212/01.wnl.0000110190.08412.25. Neurology. 2004. PMID: 14981189

6

A rare case of hypohidrotic ectodermal dysplasia caused by compound heterozygous mutations in the EDAR gene.

Shimomura Y, Sato N, Miyashita A, Hashimoto T, Ito M, Kuwano R. Shimomura Y, et al. Among authors: miyashita a. J Invest Dermatol. 2004 Oct;123(4):649-55. doi: 10.1111/j.0022-202X.2004.23405.x. J Invest Dermatol. 2004. PMID: 15373768 Free article.

7

A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease.

Ishikawa A, Piao YS, Miyashita A, Kuwano R, Onodera O, Ohtake H, Suzuki M, Nishizawa M, Takahashi H. Ishikawa A, et al. Among authors: miyashita a. Ann Neurol. 2005 Mar;57(3):429-34. doi: 10.1002/ana.20393. Ann Neurol. 2005. PMID: 15732120

8

Dynamin-binding protein gene on chromosome 10q is associated with late-onset Alzheimer's disease.

Kuwano R, Miyashita A, Arai H, Asada T, Imagawa M, Shoji M, Higuchi S, Urakami K, Kakita A, Takahashi H, Tsukie T, Toyabe S, Akazawa K, Kanazawa I, Ihara Y; Japanese Genetic Study Consortium for Alzeheimer's Disease. Kuwano R, et al. Among authors: miyashita a. Hum Mol Genet. 2006 Jul 1;15(13):2170-82. doi: 10.1093/hmg/ddl142. Epub 2006 Jun 1. Hum Mol Genet. 2006. PMID: 16740596

9

Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3.

Shimohata T, Hara K, Sanpei K, Nunomura J, Maeda T, Kawachi I, Kanazawa M, Kasuga K, Miyashita A, Kuwano R, Hirota K, Tsuji S, Onodera O, Nishizawa M, Honma Y. Shimohata T, et al. Among authors: miyashita a. Brain. 2007 Sep;130(Pt 9):2302-9. doi: 10.1093/brain/awm036. Epub 2007 Apr 2. Brain. 2007. PMID: 17405764

10

Genetic association of CTNNA3 with late-onset Alzheimer's disease in females.

Miyashita A, Arai H, Asada T, Imagawa M, Matsubara E, Shoji M, Higuchi S, Urakami K, Kakita A, Takahashi H, Toyabe S, Akazawa K, Kanazawa I, Ihara Y, Kuwano R; Japanese Genetic Study Consortium for Alzeheimer's Disease. Miyashita A, et al. Hum Mol Genet. 2007 Dec 1;16(23):2854-69. doi: 10.1093/hmg/ddm244. Epub 2007 Aug 30. Hum Mol Genet. 2007. PMID: 17761686

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