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Tsumura Research Institute For Pharmacology | 論文
- Absolute Configuration of L-Methionine Sulfoximine as a Toxic Principle in Cnestis palala (LOUR.) MERR.
- Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix.
- Effects of Gomisin A on the Promotor Action and Serum Bile Acid Concentration in Hepatocarcinogenesis Induced by 3'-Methyl-4-dimethylamino-azobenzene
- Inhibition by Gomisin A, a Lignan Compound, of Hepatocarcinogenesis by 3'-Methyl-4-dimethylaminoazobenzene in Rats
- Anti-CD3 induces bi-phasic apoptosis in murine intestinal epithelial cells : possible involvement of the Fas/Fas ligand system in different T cell compartments
- PHARMACOLOGICAL STUDIES ON GINGER. III. EFFECT OF THE SPINAL DESTRUCTION ON (6)-SHOGAOL-INDUCED PRESSOR RESPONSE IN RATS
- PHARMACOLOGICAL STUDIES ON GINGER. II. PRESSOR ACTION OF (6)-SHOGAOL IN ANESTHETIZED RATS, OR HINDQUARTERS, TAIL AND MESENTERIC VASCULAR BEDS OF RATS
- PHARMACOLOGICAL STUDIES ON GINGER. I. PHARMACOLOGICAL ACTIONS OF PUNGENT CONSTITUENTS, (6)-GINGEROL AND (6)-SHOGAOL
- VOMITING INDUCTION BY IPECAC SYRUP IN DOGS AND FERRETS
- PHARMACOLOGICAL STUDIES ON IRIDOID COMPOUNDS. II. RELATIONSHIP BETWEEN STRUCTURES AND CHOLERETIC ACTIONS OF IRIDOID COMPOUNDS
- PRACTICAL SYNTHESIS AND PHARMACOLOGY OF d, 1-DIBENZOCYCLOOCTADIENE LIGNANS
- PHARMACOLOGICAL STUDIES ON IRIDOID COMPOUNDS. III. THE CHOLERETIC MECHANISM OF IRIDOID COMPOUNDS
- CHEMICALLY INDUCED FRAGMENTATION OF MURINE ERYTHROCYTES
- EFFECTS OF LIGNAN COMPONENTS FROM SCHIZANDRA FRUITS ON EXPERIMENTAL LIVER INJURIES
- PROTECTIVE EFFECTS OF JUZENTAIHOTO, DRIED DECOCTUM OF 10 CHINESE HERBS MIXTURE, UPON THE ADVERSE EFFECTS OF MITOMYCIN C IN MICE
- The Contents of Urinary and Plasma Catecholamine Conjugate in SHR and SHRSP
- Effects of gomisin A on liver functions in hepatotoxic chemicals-treated rats.
- Effects of Gomisin A on Hepatocarcinogenesis by 3'-Methyl-4-dimethylaminoazobenzene in Rats.
- An analysis of the depressant effect of indomethacin on contractions of isolated and perfused rat hearts.
- Selective suppression of schedule-induced ethanol drinking by antialcoholic drugs in rats.