Arai Y - Search Results

1

Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.

Ichikawa M, Arai Y, Haruta M, Furukawa S, Ariga T, Kajii T, Kaneko Y. Ichikawa M, et al. Among authors: arai y. Genes Chromosomes Cancer. 2013 Mar;52(3):274-86. doi: 10.1002/gcc.22027. Epub 2012 Dec 8. Genes Chromosomes Cancer. 2013. PMID: 23225212

2

Identification of chromosome arm 9p as the most frequent target of homozygous deletions in lung cancer.

Sato M, Takahashi K, Nagayama K, Arai Y, Ito N, Okada M, Minna JD, Yokota J, Kohno T. Sato M, et al. Among authors: arai y. Genes Chromosomes Cancer. 2005 Dec;44(4):405-14. doi: 10.1002/gcc.20253. Genes Chromosomes Cancer. 2005. PMID: 16114034

3

Homozygous deletion scanning of the lung cancer genome at a 100-kb resolution.

Nagayama K, Kohno T, Sato M, Arai Y, Minna JD, Yokota J. Nagayama K, et al. Among authors: arai y. Genes Chromosomes Cancer. 2007 Nov;46(11):1000-10. doi: 10.1002/gcc.20485. Genes Chromosomes Cancer. 2007. PMID: 17674361

4

Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities.

Haruta M, Arai Y, Sugawara W, Watanabe N, Honda S, Ohshima J, Soejima H, Nakadate H, Okita H, Hata J, Fukuzawa M, Kaneko Y. Haruta M, et al. Among authors: arai y. Genes Chromosomes Cancer. 2008 Aug;47(8):712-27. doi: 10.1002/gcc.20572. Genes Chromosomes Cancer. 2008. PMID: 18464243

5

Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes.

Furukawa S, Haruta M, Arai Y, Honda S, Ohshima J, Sugawara W, Kageyama Y, Higashi Y, Nishida K, Tsunematsu Y, Nakadate H, Ishii M, Kaneko Y. Furukawa S, et al. Among authors: arai y. Cancer Sci. 2009 Apr;100(4):698-708. doi: 10.1111/j.1349-7006.2009.01102.x. Epub 2009 Feb 24. Cancer Sci. 2009. PMID: 19245437 Free PMC article.

6

Alteration of enhancer of polycomb 1 at 10p11.2 is one of the genetic events leading to development of adult T-cell leukemia/lymphoma.

Nakahata S, Saito Y, Hamasaki M, Hidaka T, Arai Y, Taki T, Taniwaki M, Morishita K. Nakahata S, et al. Among authors: arai y. Genes Chromosomes Cancer. 2009 Sep;48(9):768-76. doi: 10.1002/gcc.20681. Genes Chromosomes Cancer. 2009. PMID: 19484761

7

Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor.

Ohshima J, Haruta M, Arai Y, Kasai F, Fujiwara Y, Ariga T, Okita H, Fukuzawa M, Hata J, Horie H, Kaneko Y. Ohshima J, et al. Among authors: arai y. Genes Chromosomes Cancer. 2009 Dec;48(12):1037-50. doi: 10.1002/gcc.20705. Genes Chromosomes Cancer. 2009. PMID: 19760604

8

Genome-wide analysis of allelic imbalances reveals 4q deletions as a poor prognostic factor and MDM4 amplification at 1q32.1 in hepatoblastoma.

Arai Y, Honda S, Haruta M, Kasai F, Fujiwara Y, Ohshima J, Sasaki F, Nakagawara A, Horie H, Yamaoka H, Hiyama E, Kaneko Y. Arai Y, et al. Genes Chromosomes Cancer. 2010 Jul;49(7):596-609. doi: 10.1002/gcc.20770. Genes Chromosomes Cancer. 2010. PMID: 20461752

9

Association of germline or somatic TP53 missense mutation with oncogene amplification in tumors developed in patients with Li-Fraumeni or Li-Fraumeni-like syndrome.

Sugawara W, Arai Y, Kasai F, Fujiwara Y, Haruta M, Hosaka R, Nishida K, Kurosumi M, Kobayashi Y, Akagi K, Kaneko Y. Sugawara W, et al. Among authors: arai y. Genes Chromosomes Cancer. 2011 Jul;50(7):535-45. doi: 10.1002/gcc.20878. Epub 2011 Apr 11. Genes Chromosomes Cancer. 2011. PMID: 21484931

10

Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children.

Haruta M, Arai Y, Watanabe N, Fujiwara Y, Honda S, Ohshima J, Kasai F, Nakadate H, Horie H, Okita H, Hata J, Fukuzawa M, Kaneko Y. Haruta M, et al. Among authors: arai y. Cancer Sci. 2012 Jun;103(6):1129-35. doi: 10.1111/j.1349-7006.2012.02269.x. Epub 2012 Apr 19. Cancer Sci. 2012. PMID: 22409817 Free PMC article.

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