Watanabe N - Search Results

1

Biology of neuroblastomas that were found by mass screening at 6 months of age in Japan.

Kaneko Y, Kobayashi H, Watanabe N, Tomioka N, Nakagawara A. Kaneko Y, et al. Among authors: watanabe n. Pediatr Blood Cancer. 2006 Mar;46(3):285-91. doi: 10.1002/pbc.20496. Pediatr Blood Cancer. 2006. PMID: 16078225

2

Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma.

Sugawara W, Haruta M, Sasaki F, Watanabe N, Tsunematsu Y, Kikuta A, Kaneko Y. Sugawara W, et al. Among authors: watanabe n. Pediatr Blood Cancer. 2007 Sep;49(3):240-9. doi: 10.1002/pbc.21031. Pediatr Blood Cancer. 2007. PMID: 16937357

3

Methylation of the RASSF1A promoter is predictive of poor outcome among patients with Wilms tumor.

Ohshima J, Haruta M, Fujiwara Y, Watanabe N, Arai Y, Ariga T, Okita H, Koshinaga T, Oue T, Hinotsu S, Nakadate H, Horie H, Fukuzawa M, Kaneko Y. Ohshima J, et al. Among authors: watanabe n. Pediatr Blood Cancer. 2012 Sep;59(3):499-505. doi: 10.1002/pbc.24093. Epub 2012 Mar 27. Pediatr Blood Cancer. 2012. PMID: 22457227

4

Cryptic t(12;15)(p13;q26) producing the ETV6-NTRK3 fusion gene and no loss of IGF2 imprinting in congenital mesoblastic nephroma with trisomy 11: fluorescence in situ hybridization and IGF2 allelic expression analysis.

Watanabe N, Kobayashi H, Hirama T, Kikuta A, Koizumi S, Tsuru T, Kaneko Y. Watanabe N, et al. Cancer Genet Cytogenet. 2002 Jul 1;136(1):10-6. doi: 10.1016/s0165-4608(02)00529-0. Cancer Genet Cytogenet. 2002. PMID: 12165445

5

Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification, in neuroblastoma tumors.

Fukushi D, Watanabe N, Kasai F, Haruta M, Kikuchi A, Kikuta A, Kato K, Nakadate H, Tsunematsu Y, Kaneko Y. Fukushi D, et al. Among authors: watanabe n. Cancer Genet Cytogenet. 2009 Jan 1;188(1):32-41. doi: 10.1016/j.cancergencyto.2008.08.014. Cancer Genet Cytogenet. 2009. PMID: 19061778

6

Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type.

Watanabe N, Haruta M, Soejima H, Fukushi D, Yokomori K, Nakadate H, Okita H, Hata JI, Fukuzawa M, Kaneko Y. Watanabe N, et al. Genes Chromosomes Cancer. 2007 Oct;46(10):929-35. doi: 10.1002/gcc.20481. Genes Chromosomes Cancer. 2007. PMID: 17639583

7

Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor.

Watanabe N, Nakadate H, Haruta M, Sugawara W, Sasaki F, Tsunematsu Y, Kikuta A, Fukuzawa M, Okita H, Hata J, Soejima H, Kaneko Y. Watanabe N, et al. Genes Chromosomes Cancer. 2006 Jun;45(6):592-601. doi: 10.1002/gcc.20321. Genes Chromosomes Cancer. 2006. PMID: 16518847

8

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: watanabe n. 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.

9

Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.

Haruta M, Matsumoto Y, Izumi H, Watanabe N, Fukuzawa M, Matsuura S, Kaneko Y. Haruta M, et al. Among authors: watanabe n. Mol Carcinog. 2008 Sep;47(9):660-6. doi: 10.1002/mc.20412. Mol Carcinog. 2008. PMID: 18286482

10

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: watanabe n. Genes Chromosomes Cancer. 2008 Aug;47(8):712-27. doi: 10.1002/gcc.20572. Genes Chromosomes Cancer. 2008. PMID: 18464243

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