Zobrazeno 1 - 6
of 6
pro vyhledávání: '"11"'
Publikováno v:
The Journal of Toxicological Sciences. 32:565-570
The purpose of the present investigation is to evaluate the restraining effects of protecting jackets attached from the pre-mating period and thereafter up to completion of the fetal organogenesis in rabbits. Forty (40) Kbl:NZW mated rabbits 6 to 10
Autor:
Shuichi Kai, Eiko Hiraiwa, Kayo Sakakura, Kohji Kuroyanagi, Hiroshi Kondoh, Hirotaka Chikazawa, Norimichi Hattori, Katsumi Ishikawa, Shigeo Kawano, Toshihito Kadota, Hisashi Kohmura, Norimitsu Takahashi, Shigeru Koizumi
Publikováno v:
The Journal of Toxicological Sciences. 19:69-91
Paclitaxel, an antineoplastic agent, was administered intravenously to pregnant Crj: CD (SD) rats daily at dose levels of 0 (saline and vehicle), 0.15, 0.3 and 0.6 mg/kg from day 7 to day 17 of gestation. Results were as follows: 1. The ossification
Publikováno v:
The Journal of Toxicological Sciences. 18:1-17
A teratogenicity study was carried out in Sprague-Dawley rats subcutaneously injected recombinant Granulocyte-Macrophage Colony Stimulating Factors (LBD-005), the growth of stem cell and the development of the hematopoietic cell, at dose levels of 25
Publikováno v:
The Journal of Toxicological Sciences. 10:203-226
A teratogenicity study was carried out in S1c: SD rats orally administered Hydroxypropylmethylcellulose acetate succinate (HPMCAS), a useful pharmaceutical excipient, at dose levels of 625, 1,250 and 2,500 mg/kg/day for a period of 11 days from day 7
Publikováno v:
The Journal of Toxicological Sciences. 9:109-126
A teratogenicity study on bromperidol, a neuroleptic, was carried out in Wistar-Imamichi rats. Bromperidol was administered orally at the dose levels of 0.2, 1.5 and 10.0 mg/kg/day for 11 days from day 7 to day 17 of gestation. About two-thirds of pr
Autor:
Tsuneyoshi Tanabe, Masako Sakanoue, Satoru Kamada, Noriko Higashida, K Simpo, Masaya Takeuchi
Publikováno v:
The Journal of Toxicological Sciences. 8:101-122
A teratogenicity study was carried out in Crj: CD (SD) rats orally administered ranitidine hydrochloride, a histamine H2-receptor antagonist, at dose levels of 50, 200 and 800 mg/kg/day as base weight for a period of 11 days from day 7 to day 17 of g