Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kazuo, Kizawa"'
Autor:
Yasuni Nakanuma, Mitsue Yasoshima, Shinichi Furubo, Yasunori Sato, Kenichi Harada, Takahiro Sanzen, Kazuo Kizawa, Satoru Ozaki
Publikováno v:
The Journal of Pathology. 217:442-451
Congenital hepatic fibrosis (CHF) and Caroli's disease are though to result from ductal plate malformation, and the basal laminar components play important roles in biliary differentiation during development. To clarify the involvement of basal lamin
Autor:
Takayuki Matsuno, Yusuke Nozaki, Takahiro Sanzen, Rie Fukui, T. Kozaki, Eiko Furubo, Kazuo Kizawa
Publikováno v:
The Journal of Toxicological Sciences. 34:S73-S81
The main aim of the present study is to determine the optimal administration period of cisplatin with regards to its toxic effects on ovarian morphology in the repeated-dose toxicity study. Cisplatin was administered to female SD rats intraperitoneal
Publikováno v:
Journal of Infection and Chemotherapy. 9:144-150
The therapeutic efficacy of amphotericin B (AmB), imipenem/cilastatin (IPM/CS), pazufloxacin (PZFX) mesilate, and combinations of these, was evaluated using an experimental pulmonary superinfection model in mice caused by Pseudomonas aeruginosa and A
Publikováno v:
Journal of Toxicologic Pathology. 15:69-72
Cardiac rhabdomyoma was found as an incidental finding in a 6-month-old male beagle dog on microscopic examination. The lesions took a spongy appearance and were located in the subepicardial area of the juncion of the left ventricular wall and the in
Publikováno v:
The Journal of Toxicological Sciences. 25:187-194
The toxicity of Enoxacin (ENX), a fluoroquinolone antibacterial agent, on the testis and epididymis was studied in rats. ENX was administered to 5 male rats orally once daily for 2 weeks at the dose level of 3000 mg/kg/day. ENX-treated rats showed a
Autor:
Kumiko Isse, Satoru Ozaki, Motoko Sasaki, Mitsue Yasoshima, Yasuni Nakanuma, Takahiro Sanzen, Shinichi Furubo, Yasunori Sato, Kenichi Harada, Kazuo Kizawa
The polycystic kidney (PCK) rat represents a liver and kidney cyst pathology corresponding to Caroli's disease with congenital hepatic fibrosis and autosomal recessive polycystic kidney disease. We previously reported that an epidermal growth factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cd343ef78d0bbb6390e99dbeee3f6e8
https://europepmc.org/articles/PMC1698840/
https://europepmc.org/articles/PMC1698840/
Autor:
Takahiro Sanzen, Yasuni Nakanuma, Kenichi Harada, Mitsue Yasoshima, Kazuo Kizawa, Masahiko Ishibashi, Shinichi Furubo, Yasunori Sato, Satoru Ozaki
Publikováno v:
The American journal of pathology. 166(1)
Polycystic kidney (PCK) rats exhibit a multiorgan cyst pathology similar to human autosomal recessive polycystic kidney disease, and are proposed as an animal model of Caroli’s disease with congenital hepatic fibrosis (CHF). This study investigated
Autor:
Kazuo, Kizawa, Miyono, Miyazaki, Mineko, Nagasawa, Naoko, Ogake, Akio, Nagai, Takahiro, Sanzen, Yasuhito, Kawamura
Publikováno v:
The Japanese journal of antibiotics. 56(1)
The protective effect of pazufloxacin (PZFX) mesilate, a parenteral quinolone antimicrobial agent, on arbekacin (ABK)-induced nephrotoxicity was evaluated with 8-week-old male Sprague-Dawley rats. Animals were injected with ABK at a dose of 32 mg/kg
Autor:
Teiichi Morita, Kazuo Kizawa, Yasuhito Kawamura, Hiroyuki Fukumoto, Shinichi Furubo, Takahiro Sanzen, Miyono Miyazaki, Hiroyoshi Hayakawa, Akio Nagai
Publikováno v:
The Journal of toxicological sciences. 27(3)
The articular toxicity of garenoxacin (formerly T-3811 or BMS-284756) was experimentally examined utilizing juvenile beagle dogs. Garenoxacin and two other reference quinolones were administered at intravenous dosages of 30 and 60 mg/kg. Each group c
Autor:
Shinzaburo Minami, Ritsuko Hori, Yozo Todo, Hirokazu Narita, Yasuo Watanabe, Masako Shimakura, Masahiro Takahata, Kazuo Kizawa
Publikováno v:
Antimicrobial agents and chemotherapy. 45(1)
T-3811, the free base of T-3811ME (BMS-284756), a new des-F(6)-quinolone, showed a potent in vitro activity (MIC at which 90% of the isolates tested are inhibited [MIC 90 ], 0.0313 μg/ml) against Mycoplasma pneumoniae . The MIC 90 of T-3811 was 4-fo