Kunio Hori
Olympus Corporation
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Publication
Featured researches published by Kunio Hori.
Cancer Cell | 2016
Shinichi Yachida; Laura D. Wood; Masami Suzuki; Erina Takai; Yasushi Totoki; Mamoru Kato; Claudio Luchini; Yasuhito Arai; Hiromi Nakamura; Natsuko Hama; Asmaa Elzawahry; Fumie Hosoda; Tomoki Shirota; Nobuhiko Morimoto; Kunio Hori; Jun Funazaki; Hikaru Tanaka; Chigusa Morizane; Takuji Okusaka; Satoshi Nara; Kazuaki Shimada; Nobuyoshi Hiraoka; Hirokazu Taniguchi; Ryota Higuchi; Minoru Oshima; Keiichi Okano; Seiko Hirono; Masamichi Mizuma; Koji Arihiro; Masakazu Yamamoto
Ampullary carcinomas are highly malignant neoplasms that can have either intestinal or pancreatobiliary differentiation. To characterize somatic alterations in ampullary carcinomas, we performed whole-exome sequencing and DNA copy-number analysis on 60 ampullary carcinomas resected from clinically well-characterized Japanese and American patients. We next selected 92 genes and performed targeted sequencing to validate significantly mutated genes in an additional 112 cancers. The prevalence of driver gene mutations in carcinomas with the intestinal phenotype is different from those with the pancreatobiliary phenotype. We identified a characteristic significantly mutated driver gene (ELF3) as well as previously known driver genes (TP53, KRAS, APC, and others). Functional studies demonstrated that ELF3 silencing in normal human epithelial cells enhances their motility and invasion.
Proceedings of SPIE | 2014
Mitsushiro Yamaguchi; Tetsuya Tanabe; Hidetaka Nakata; Takuya Hanashi; Kazutaka Nishikawa; Kunio Hori; Seiji Kondo
A new, simple technique for single molecule fluorescence detection has been developed and detection limit of less than 100 aM fluorophores has been demonstrated. The technique, similarly to Fluorescence Correlation Spectroscopy (FCS) and other related techniques, uses confocal optics, but differs in that it detects individual molecules crossing the inside of a scanning confocal volume without using statistical techniques as applied in FCS or similar methods. The scanning speed of the confocal volume is higher than the Brownian motion speed of the molecules. Thus, the time evolution of the light intensity data reflects the confocal volume intensity profile, which clearly shows the crossing of single molecules. The estimated total scanning volume enables the concentration or the density of molecules to be obtained. In addition, information related to the rotational and translational diffusion of the molecule was obtained for the purpose of identifying different molecules. It was shown that utilizing the plural characteristic properties of molecules passing through a confocal volume makes possible the discrimination of different molecules. The proposed technique is based on the simple principle of counting molecules one by one using a scanning confocal volume, and is hereafter referred to as Scanning Single-Molecule Counting (SSMC).
Archive | 2011
Mitsushiro Yamaguchi; Seiji Kondo; Tetsuya Tanabe; Kunio Hori
Archive | 2011
Tetsuya Tanabe; Hidetaka Nakata; Takuya Hanashi; Kunio Hori; Kazutaka Nishikawa
Archive | 2010
Kunio Hori; Hidetaka Nakata; Sayoko Kobayashi
Archive | 2001
Kunio Hori; Sachiko Karaki; Tokio Kano; Yuji Takamiya
Archive | 2013
Kunio Hori; Kenzo Fujimoto
Archive | 2013
Tetsuya Tanabe; Hidetaka Nakata; Takuya Hanashi; Kunio Hori; Kazutaka Nishikawa
Archive | 2001
Kunio Hori; Sachiko Karaki; Tokio Kano; Yuji Takamiya
Ieej Transactions on Sensors and Micromachines | 1999
Seiji Kondo; Nobuhiko Morimoto; Kunio Hori; Etsuo Shinohara; Kyoichi Kano