Imoto I - Search Results

1

GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines.

Yu W, Inoue J, Imoto I, Matsuo Y, Karpas A, Inazawa J. Yu W, et al. Among authors: imoto i. J Hum Genet. 2003;48(6):331-335. doi: 10.1007/s10038-003-0026-2. Epub 2003 Apr 29. J Hum Genet. 2003. PMID: 12721791

2

PPM1D is a potential target for 17q gain in neuroblastoma.

Saito-Ohara F, Imoto I, Inoue J, Hosoi H, Nakagawara A, Sugimoto T, Inazawa J. Saito-Ohara F, et al. Among authors: imoto i. Cancer Res. 2003 Apr 15;63(8):1876-83. Cancer Res. 2003. PMID: 12702577

3

Overexpression of PDZK1 within the 1q12-q22 amplicon is likely to be associated with drug-resistance phenotype in multiple myeloma.

Inoue J, Otsuki T, Hirasawa A, Imoto I, Matsuo Y, Shimizu S, Taniwaki M, Inazawa J. Inoue J, et al. Among authors: imoto i. Am J Pathol. 2004 Jul;165(1):71-81. doi: 10.1016/S0002-9440(10)63276-2. Am J Pathol. 2004. PMID: 15215163 Free PMC article.

4

Frequent silencing of DBC1 is by genetic or epigenetic mechanisms in non-small cell lung cancers.

Izumi H, Inoue J, Yokoi S, Hosoda H, Shibata T, Sunamori M, Hirohashi S, Inazawa J, Imoto I. Izumi H, et al. Among authors: imoto i. Hum Mol Genet. 2005 Apr 15;14(8):997-1007. doi: 10.1093/hmg/ddi092. Epub 2005 Mar 3. Hum Mol Genet. 2005. PMID: 15746151

5

Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.

Hayashi S, Kurosawa K, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: imoto i. Am J Med Genet A. 2005 Nov 15;139(1):32-6. doi: 10.1002/ajmg.a.30982. Am J Med Genet A. 2005. PMID: 16222686

6

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: imoto i. J Hum Genet. 2007;52(5):397-405. doi: 10.1007/s10038-007-0127-4. Epub 2007 Apr 4. J Hum Genet. 2007. PMID: 17406783

7

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: imoto i. 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

8

Novel targets for the 18p11.3 amplification frequently observed in esophageal squamous cell carcinomas.

Nakakuki K, Imoto I, Pimkhaokham A, Fukuda Y, Shimada Y, Imamura M, Amagasa T, Inazawa J. Nakakuki K, et al. Among authors: imoto i. Carcinogenesis. 2002 Jan;23(1):19-24. doi: 10.1093/carcin/23.1.19. Carcinogenesis. 2002. PMID: 11756219

9

TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas.

Yasui K, Arii S, Zhao C, Imoto I, Ueda M, Nagai H, Emi M, Inazawa J. Yasui K, et al. Among authors: imoto i. Hepatology. 2002 Jun;35(6):1476-84. doi: 10.1053/jhep.2002.33683. Hepatology. 2002. PMID: 12029633

10

The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation.

Saito-Ohara F, Fukuda Y, Ito M, Agarwala KL, Hayashi M, Matsuo M, Imoto I, Yamakawa K, Nakamura Y, Inazawa J. Saito-Ohara F, et al. Among authors: imoto i. Am J Hum Genet. 2002 Sep;71(3):637-45. doi: 10.1086/342208. Epub 2002 Jul 23. Am J Hum Genet. 2002. PMID: 12145744 Free PMC article.

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