Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maiko Okamoto"'
Autor:
Masahito Nosé, Atsuki Shinbori, Yoshizumi Miyoshi, Tomoaki Hori, Tsukasa Ohira, Junko Hashiba, Chizuko Naoe, Rui Gakiya, Maiko Okamoto, Takeshi Sagara, Takaaki Aoki, Shigeki Matsubara, Ichiro Takahashi, Hidekazu Hayashi, Kazunari Yamada, Yasuyuki Minamiyama, Yoshimasa Tanaka, Shuji Abe, Satoru UeNo, Shun Imajo, Yasuo Saito, Takuya Ashikita, Yuko Hori, Toshiyuki Shimizu, Nanako Okamura, Kaoru Hirano, Lee Bargatze
Publikováno v:
Data Science Journal, Vol 23, Pp 40-40 (2024)
This paper outlines our practice to enhance the findability and searchability of research data through metadata conversion from the Space Physics Archive Search and Extract (SPASE) schema to a more generic schema, the Japan Consortium for Open Access
Externí odkaz:
https://doaj.org/article/be33d75c0a0348a4888d5a736816cdc1
Autor:
Nobuhisa Takase, Manabu Shigeoka, Yoshihiro Kakeji, Himiko Kodaira, Masayoshi Hosono, Hiroshi Yokozaki, Yu-ichiro Koma, Nobuhide Higashino, Mari Nishio, Maiko Okamoto
Publikováno v:
Laboratory Investigation. 99:777-792
Esophageal squamous cell carcinoma (ESCC) is a highly aggressive tumor with frequent recurrence even after curative resection. The tumor microenvironment, which consists of non-cancer cells, such as cancer-associated fibroblasts (CAFs) and tumor-asso
Publikováno v:
Regulatory Toxicology and Pharmacology. 113:104617
Read-across based on only structural similarity is considered to have a risk of error in chemical risk assessment. Under these circumstances, considering biological similarity based on adverse outcome pathways using in vitro omics technologies is exp
Publikováno v:
Limnology. 11:167-170
Seasonal dynamics of the fish parasite Neoplagioporus ayu (Digenea; Opecoelidae; Plagioporinae) in its definitive host, the ayu Plecoglossus altivelis, in the Chikugo River, Kyushu, Japan, was examined. Natural ayu are amphidromous. In the upper Chik
Publikováno v:
Chemicalpharmaceutical bulletin. 51(6)
Diffusion coefficients (D) of parabens and steroids in water and 1-octanol were determined by using the chromatographic broadening method at 37 degrees C, and the relationships between the D values and the physicochemical properties of the drugs were