Okazawa H - Search Results

1

Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.

Honda S, Hayashi S, Imoto I, Toyama J, Okazawa H, Nakagawa E, Goto Y, Inazawa J. Honda S, et al. Among authors: okazawa h. J Hum Genet. 2010 Sep;55(9):590-9. doi: 10.1038/jhg.2010.74. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613765

2

PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival.

Waragai M, Lammers CH, Takeuchi S, Imafuku I, Udagawa Y, Kanazawa I, Kawabata M, Mouradian MM, Okazawa H. Waragai M, et al. Among authors: okazawa h. Hum Mol Genet. 1999 Jun;8(6):977-87. doi: 10.1093/hmg/8.6.977. Hum Mol Genet. 1999. PMID: 10332029

3

A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family.

Takano K, Nakagawa E, Inoue K, Kamada F, Kure S, Goto Y; Japanese Mental Retardation Consortium. Takano K, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):479-84. doi: 10.1002/ajmg.b.30638. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18081026

4

Knock-down of PQBP1 impairs anxiety-related cognition in mouse.

Ito H, Yoshimura N, Kurosawa M, Ishii S, Nukina N, Okazawa H. Ito H, et al. Among authors: okazawa h. Hum Mol Genet. 2009 Nov 15;18(22):4239-54. doi: 10.1093/hmg/ddp378. Epub 2009 Aug 6. Hum Mol Genet. 2009. PMID: 19661183

5

Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.

Honda S, Satomura S, Hayashi S, Imoto I, Nakagawa E, Goto Y, Inazawa J; Japanese Mental Retardation Consortium. Honda S, et al. J Hum Genet. 2012 Jan;57(1):73-7. doi: 10.1038/jhg.2011.131. Epub 2011 Dec 1. J Hum Genet. 2012. PMID: 22129561

6

Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1.

Barclay SS, Tamura T, Ito H, Fujita K, Tagawa K, Shimamura T, Katsuta A, Shiwaku H, Sone M, Imoto S, Miyano S, Okazawa H. Barclay SS, et al. Among authors: okazawa h. Hum Mol Genet. 2014 Mar 1;23(5):1345-64. doi: 10.1093/hmg/ddt524. Epub 2013 Oct 31. Hum Mol Genet. 2014. PMID: 24179173

7

PQBP-1 transgenic mice show a late-onset motor neuron disease-like phenotype.

Okuda T, Hattori H, Takeuchi S, Shimizu J, Ueda H, Palvimo JJ, Kanazawa I, Kawano H, Nakagawa M, Okazawa H. Okuda T, et al. Among authors: okazawa h. Hum Mol Genet. 2003 Apr 1;12(7):711-25. doi: 10.1093/hmg/ddg084. Hum Mol Genet. 2003. PMID: 12651867

8

Nematode homologue of PQBP1, a mental retardation causative gene, is involved in lipid metabolism.

Takahashi K, Yoshina S, Masashi M, Ito W, Inoue T, Shiwaku H, Arai H, Mitani S, Okazawa H. Takahashi K, et al. Among authors: okazawa h. PLoS One. 2009;4(1):e4104. doi: 10.1371/journal.pone.0004104. Epub 2009 Jan 1. PLoS One. 2009. PMID: 19119319 Free PMC article.

9

Ataxin-7 associates with microtubules and stabilizes the cytoskeletal network.

Nakamura Y, Tagawa K, Oka T, Sasabe T, Ito H, Shiwaku H, La Spada AR, Okazawa H. Nakamura Y, et al. Among authors: okazawa h. Hum Mol Genet. 2012 Mar 1;21(5):1099-110. doi: 10.1093/hmg/ddr539. Epub 2011 Nov 18. Hum Mol Genet. 2012. PMID: 22100762 Free PMC article.

10

Comprehensive phosphoproteome analysis unravels the core signaling network that initiates the earliest synapse pathology in preclinical Alzheimer's disease brain.

Tagawa K, Homma H, Saito A, Fujita K, Chen X, Imoto S, Oka T, Ito H, Motoki K, Yoshida C, Hatsuta H, Murayama S, Iwatsubo T, Miyano S, Okazawa H. Tagawa K, et al. Among authors: okazawa h. Hum Mol Genet. 2015 Jan 15;24(2):540-58. doi: 10.1093/hmg/ddu475. Epub 2014 Sep 17. Hum Mol Genet. 2015. PMID: 25231903

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