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Publication
Featured researches published by K. Imanishi.
Cancer | 1992
Hiroyasu Lishi; Masaharu Tatsuta; Shusaku Tsutsui; K. Imanishi; Tom Otani; Shigeru Okuda; Shingo Ishiguro; Haruo Taniguchi
From January 1987 to December 1990, five cases of early depressed cancer of the large intestine were seen. Endo‐scopically, almost all of these tumors were located in the proximal colon and looked like a reddish depression (similar to the sucker of an octopus). Histologically, all of these cancers were well differentiated and tended to reach deeper layers at an early stage. Four (80%) of these cancers were not associated with adenoma and were thought to have arisen de novo. Cancer 1992; 69:2406‐2410.
Cancer Letters | 2000
Masaru Murata; Kyoko Iwao; Yasuo Miyoshi; Yutaka Nagasawa; Michihiro Yabu; Seiichi Himeno; K. Imanishi; Masahiko Ohsawa; Hisashi Wada; Shusei Tominaga; Takashi Shimano; Tetsuro Kobayashi; Yusuke Nakamura
beta-Catenin has been identified as an oncogene in several tumors including colorectal cancers. beta-Catenin gene is activated by interstitial deletions involving exon 3 in colorectal carcinomas of Japanese population, in contrast to amino acid substitutions detected among Caucasian population. The aim of this study was to examine the type and frequency of beta-catenin gene mutation during early stages of colorectal tumorigenesis. We screened 100 colorectal adenomas for somatic mutations in the beta-catenin gene by single-strand conformation polymorphism method, as well as polymerase chain reaction amplification. In cases with mutations, sequencing analyses and immunohistochemical staining were also performed. Somatic interstitial deletions of 272-413 bp, each of which included all parts of exon 3, were detected in three tumors. However, no adenoma carried missense mutations. We confirmed accumulation of aberrant beta-catenin protein in cytoplasm and nuclei of adenoma cells by immunohistochemical analysis. Our results suggested that activation of the beta-catenin gene by interstitial deletions involving exon 3 might be less frequent compared with frequent alterations of adenomatous polyposis coli (APC) gene, but could be an early event in colorectal tumorigenesis equivalent to APC gene alterations in the Japanese population.
International Journal of Cancer | 1990
Ryosuke Murakami; Hideaki Tsukuma; Shinobu Kanamori; K. Imanishi; Toru Otani; Katsumi Nakanishi; Isaburo Fujimoto; Akira Oshima
Archive | 2007
William L. Ellsworth; Stephen H. Hickman; Mark D. Zoback; K. Imanishi; Clifford H. Thurber; Steven W. Roecker
Digestive Endoscopy | 1990
Seishiro Mimura; Makoto Ichii; K. Imanishi; Masaharu Tatsuta; Torn Otani; Shigeru Okuda
Archive | 2006
Naoshige Uchida; William L. Ellsworth; Tetsuro Matsuzawa; K. Imanishi; Takashi Okada; Akira Hasegawa
Archive | 2008
Satoshi Itaba; Naoto Koizumi; Maiko Takahashi; Naoyuki Matsumoto; Ryu Ohtani; Yoneyoshi Kitagawa; K. Imanishi; N. Takeda
Archive | 2004
Tsuyoshi Takeda; Yuji Kuwahara; Tadanori Mizuno; K. Imanishi; Takashi Okada; Kazufumi Ito; H. Garrett Wada; Yoshikatsu Haryu
THE JOURNAL OF JAPAN SOCIETY FOR LASER SURGERY AND MEDICINE | 1987
Seishiro Mimura; Makoto Ichii; K. Imanishi; Toru Otani; Shigeru Okuda
Archive | 2010
William L. Ellsworth; K. Imanishi