Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Toshiwo Andoh"'
Autor:
Hiroshi Mizunuma, Satoshi Suzuki, Chiyo Oukouchi, Kensuke Kumamoto, Yoshiko Matsumoto, Toshiwo Andoh, Manabu Iwadate, Shinichi Suzuki, Seiichi Takenoshita
Publikováno v:
Annals of Cancer Research and Therapy. 26:77-81
Publikováno v:
Progress in Nonhistone Protein Research ISBN: 9781351076067
Progress in Nonhistone Protein Research
Progress in Nonhistone Protein Research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f659bec76b50ef4e243eb38030a8aa8
https://doi.org/10.1201/9781351076067-8
https://doi.org/10.1201/9781351076067-8
Autor:
Norio Takahashi, Yasushi Okazaki, Igor V. Kurochkin, Toshiwo Andoh, Aliaksandr A. Yarmishyn, Hiroyoshi Iseki, Hideaki Shimada, Akihiko Takeda, Isamu Koyama
Publikováno v:
Cancer Science. 101:1361-1366
The aberrant activation of Wnt signaling is a key process in colorectal tumorigenesis. Canonical Wnt signaling controls transcription of target genes via beta-catenin and T-cell factor/lymphoid enhancer factor family transcription factor complex. Arm
Autor:
Banri Yamanoha, Atsushi Numata, Toshiwo Andoh, Takao Yamori, Masahito Shinomi, Tetsuo Sugahara, Izumi Yamashita, Noriko Sasaki-Takahashi, Miyako Yanagihara, Seiko Yamamoto, Masashi Hayashida
Publikováno v:
Cancer Science. 96:816-824
DNA topoisomerases (topo) I and II are molecular targets of several potent anticancer agents. Thus, inhibitors of these enzymes are potential candidates or model compounds for anticancer drugs. Leptosins (Leps) F and C, indole derivatives, were isola
Publikováno v:
Biochemical and Biophysical Research Communications. 301:798-803
BAG-1 was originally identified as a binding partner of anti-apoptotic factor Bcl-2 [Takayama et al., Cell 80 (1995) 279-284]. Exogenous expression of BAG-1 was reported to confer cells resistance to several stresses [Chen et al., Oncogene 21 (2002)
Autor:
Naoko Yamagaki, Chika Iwamoto, Yoshimasa Uehara, Atsushi Numata, Toshiwo Andoh, Ken Umemura, Takeshi Yamada, Takao Yamori, Takako Yamanouchi, Katsuhiko Minoura
Publikováno v:
Tetrahedron. 58:479-487
Leptosins M ( 4 ), M1 ( 5 ) N ( 6 ) and N1 ( 7 ) have been isolated from a strain of Leptosphaeria sp. originally separated from the marine alga Sargassum tortile. Their absolute stereostructures have been elucidated by spectral analyses and some che
Autor:
Shinichi Takayama, Toshiwo Andoh, John C. Reed, Junko Takahashi, Noriko Takahashi, Reiko Sasaki
Publikováno v:
Biochemical and Biophysical Research Communications. 286:807-814
BAG-1M, one of the isoforms of BAG-1, was reported to bind to DNA and stimulate general transcription when cells were stressed by heat shock (Zeiner, M., et al., Proc. Natl. Acad. Sci. USA 96, 10194-10199, 1999). Here we show that BAG-1M binds and en
Autor:
Kae Yanase, Tomoko Oh-hara, Toshiwo Andoh, Yoshikazu Sugimoto, Takashi Tsuruo, Satomi Tsukahara
Publikováno v:
Japanese Journal of Cancer Research : Gann
In previous studies, we established two camptothecin (CPT)-resistant sublines, HT-29 / CPT and St-4 / CPT, from the human colon cancer cell line HT-29 and the human stomach cancer cell line St-4, respectively. Cellular contents of DNA topoisomerase I
Autor:
Ken Kodama, Akira Togayachi, Shoko Nishihara, Hisashi Narimatsu, Masahiko Higashiyama, Yuzuru Ikehara, Hiroko Iwasaki, Toshiwo Andoh, Takashi Kudo, Shoji Nakamori
Publikováno v:
International Journal of Cancer. 83:70-79
Sialyl Lewis a and x antigens are well-known tumor-associated antigens expressed in many cancer tissues. The expression of the genes encoding 5 alpha1,3fucosyltransferases, which are able to synthesize the sialyl Lewis antigens, was examined in norma
Autor:
Seiichi Sato, Ryusuke Nakagawa, Yasuyo Suga, Ken Umemura, Toshiwo Andoh, Toshihiko Yoshimura, Takashi Tsuji
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 9:2653-2656
A series of methoxycarbonyl group modified nidulalin A analogs were synthesized to improve stability against esterases. The amide derivatives showed cytotoxic activity along with inhibitory activity against DNA topoisomerase II. Among the analogs, am