Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Akira Wakui"'
Autor:
Nobuteru Kikkawa, Keisuke Aiba, Yasushi Mitachi, Kazuo Shirouzu, Minoru Kurihara, Akira Wakui, Noboru Horikoshi, Yuh Sakata, Atsushi Sato
Publikováno v:
Anti-Cancer Drugs. 10:741-748
Raltitrexed (Tomudex), a novel folate-based inhibitor of thymidylate synthase, has demonstrated anti-tumour efficacy comparable with 5-fluorouracil and leucovorin in patients with advanced colorectal cancer (CRC). This phase II study was conducted to
Publikováno v:
Japanese Journal of Phytopathology. 62:69-74
北海道,北見地方にはインゲンマメ根腐病(病原菌Fusarium solani f. sp. phaseoli)の発病抑止土壌(北見土壌)が存在する。この土壌では同菌大型分生子の発芽が強く阻害され,これには土壌の化学的
Autor:
Akira Wakui, H. Takahashi, Kazuo Kubota, Kazunori Sato, Hiroshi Fukuda, Roko Kubota, Ren Iwata, Takehiko Fujiwara, Hiroshi Sugiyama, Tatsuo Ido, Masao Tada
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 34:741-746
A rapid synthesis of Nω-[18F]fluoroacetylserotonin (Nω-[18F]fluoroacetyl-5-hydroxytryptamine) starting from [18F]fluoride and ethyl p-toluensulfonyloxyacetate is described. The total time required for its synthesis is ca. 90 min. The radiochemical
Autor:
Roko Kubota, Kazunori Sato, Hiroshi Fukuda, Hiroshi Sugiyama, Kazuo Kubota, Akira Wakui, H. Takahashi, Tachio Sato, Masao Tada, Yoshinao Abe, Tatsuo Ido, Ren Iwata, C. Pascali, Takehiko Fujiwara
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 33:601-606
An efficient synthesis of [fluoroacetyl-18F]fluoromelatonin (Nω-[18F]Fluoroacetyl-5-methoxytryptamine) starting from [18F]fluoride and ethyl p-toluensulfonyloxyacetate is described. The total time required for its synthesis is ca. 90 min. The radioc
Autor:
Masami Hirano, Akira Wakui, Ikurou Kimura, Ota K, Tamotsu Matsuda, Yutaka Ariyoshi, Makoto Ogawa, Takashi Yoshida, Masao Oguro, Yutaka Yoshida
Publikováno v:
Cancer Chemotherapy and Pharmacology. 31:445-448
Liblomycin (NK313) is a bleomycin analog that has proved to be associated with less pulmonary toxicity and with more potent antitumor activity than bleomycin in animal tumors. In a phase I study, pulmonary toxicity was not observed, whereas myelosupp
Autor:
Tohru Takahashi, Haruhiko Sato, Akira Wakui, Ryunosuke Kanamaru, Masahiko Hoshi, Megumi Nakamura
Publikováno v:
The Tohoku Journal of Experimental Medicine. 167:27-37
NAKAMURA, M., TAKAHASHI, T., SATO, H., HOSHI, M., WAKUI, A. and KANAMARU, R. Histopathological Evaluation on the Effect of Induced Hypertension Chemotherapy Presurgically Performed in Patients with Advanced Carcinoma of the Stomach. Tohoku J. Exp. Me
Autor:
Yoshinao Abe, Tachio Sato, Akira Wakui, H. Takahashi, Masao Tada, Atsushi Oikawa, Tatsuo Yamaguchi, Ren Iwata, Kazunori Sato, Hiroshi Fukuda, Kazuo Kubota, Tatsuo Ido, Hiroshi Sugiyama, Takehiko Fujiwara
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 29:949-955
Rapid chemical syntheses of [carbonyl- 11C]melatonin and N-[carbonyl- 11C]acetylserotonin starting from [11C]carbon dioxide are described. The radiochemical yield (based on [carbonyl-11C]-acetic acid), purity, and the specific activity (end of bombar
Autor:
Tetsuro Nishihira, Chikashi Ishioka, Akira Wakui, Ryunosuke Kanamaru, Toshiaki Sato, Konishi Y, Hiroyuki Shibata, Akira Ishikawa
Publikováno v:
Cancer. 67:2560-2564
The expression of human glutathione S-transferase-pi (GST-pi) in resected primary esophageal tumors and in matching normal esophageal mucosa from 25 patients undergoing radical surgery was measured by RNA blot hybridization. The RNA transcript levels
Autor:
Yoshinao Abe, Tatsuo Ido, Tachio Sato, Hiroshi Sugiyama, Ren Iwata, Tatsuo Yamaguchi, Akira Wakui, H. Takahashi, Atsushi Oikawa, Kazunori Sato, Kazuo Kubota, Masao Tada, Takehiko Fujiwara, Kiichi Ishiwata
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 29:485-490
A rapid chemical synthesis of 2-[carbonyl-11C]acetamido-2-deoxy-D-glucopyranose (N-[carbonyl-11C]acetyl-D-glucosamine) starting from [11C]carbon dioxide is described. The total time required for the synthesis, the radiochemical yield, and purity of t
Publikováno v:
The Tohoku Journal of Experimental Medicine. 163:279-288
Intravenously or intraperitoneally administered Chromomycin A3 (CHRM), an anticancer drug, augmented natural killer (NK) activity of both spleen cells and peritoneal exudate cells in BALB/c mice. When CHRM was administered intravenously, NK activity