Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fumio Nishikaku"'
Autor:
Fumio Nishikaku, Toshihiro Noguchi, Akemi Baba, Yasuyuki Tsutsumishita, Mitsuharu Hanada, Nobuyoshi Chiba, Takashi Yamaoka
Publikováno v:
Cancer Chemotherapy and Pharmacology
Background Miriplatin (formerly SM-11355), a novel lipophilic platinum complex developed to treat hepatocellular carcinoma, is administered into the hepatic artery using an oily lymphographic agent (Lipiodol Ultra-Fluide®) as a carrier. We clarified
Autor:
Fumio Nishikaku, Yoshihiko Koga
Publikováno v:
Immunopharmacology. 25:65-74
The antiarthritic activity of a novel thiazole derivative, SM-8849, was compared with that of indomethacin and D-penicillamine, in mice with collagen-induced arthritis. SM-8849 reduced the incidence and severity of disease in collagen-immunized mice,
Autor:
Katsumi Eguchi, Tomoki Origuchi, Hiroaki Ida, Fumiko Tanaka, Kazuhiko Arima, Makoto Kamachi, Koichiro Aratake, A. Nozomi Iwanaga, Taiichiro Miyashita, Huang Mingguo, Yasumori Izumi, Atsushi Kawakami, Kiyoshi Migita, Koto Nakashima, Shuzo Tagashira, Seigou Abiru, Fumio Nishikaku, Mami Tamai
Publikováno v:
Biochemical and biophysical research communications. 312(2)
Akt is known to be activated in the rheumatoid synovial tissues. We examined here functional role of Akt during tumor necrosis factor-related apoptosis inducing ligand (TRAIL)-mediated apoptosis in rheumatoid synovial cells. Rheumatoid synovial cells
Publikováno v:
International journal of immunopharmacology. 16(2)
To evaluate the antiarthritic properties of a novel thiazole derivative, the drugs SM-8849, D-penicillamine and indomethacin were administered to pristane-injected DBA/1 mice. The mice were treated daily with the agents for 32 weeks, starting from th
Autor:
Fumio Nishikaku, Yoshihiko Koga
Publikováno v:
International journal of immunopharmacology. 13(5)
The effects of SM-8849 on the development of autoimmune disease in MRL/Mp-1pr/1pr mice were examined. SM-8849 improved survival as well as renal disease, restored the deficits in splenic cell responsiveness to stimulation by mitogens or conventional