Zobrazeno 1 - 10
of 126
pro vyhledávání: '"U, Takeda"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
U, Takeda
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 25
Since May in 1994, we have started to take care of terminally-ill patients at home to support patients who want to die at home and their family. Many patients in the terminal stage become stable temporarily from being back home, and their family are
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 22
We had given the service to the patients who desired home care. And now we made inquiries about 16 cases died at home. They were satisfied with our service and death at home. But in regard to the question "If you die at home, Are you satisfied?¿, ha
Autor:
M, Yokota, U, Takeda, M, Odaki, H, Sasaki, T, Niizato, H, Kawaoto, H, Watanabe, N, Ishiwatari, H, Hayasaka, T, Koeda
Publikováno v:
The Japanese journal of antibiotics. 37(8)
Miocamycin (MOM) is a derivative of midecamycin and is metabolized into 4 main metabolites of Mb1, Mb2, Mb6 and Mb12. It is also known that LD50 values of Mb6 were 4,150 mg/kg in male mice and 4,000 mg/kg in female mice but LD0 values in male and fem
Autor:
M, Yokota, U, Takeda, M, Odaki, H, Sasaki, T, Niizato, H, Kawaoto, H, Watanabe, N, Ishiwatari, H, Hayasaka, T, Koeda
Publikováno v:
The Japanese journal of antibiotics. 37(8)
Miocamycin (MOM) is a derivative of midecamycin, a macrolide antibiotic and is metabolized into 4 main metabolites of Mb1, Mb2, Mb6 and Mb12. At previous study, the acute and subacute toxicity of Mb1 and acute toxicity of Mb2 were performed that thos
Autor:
M, Yokota, U, Takeda, M, Odaki, H, Sasaki, T, Niizato, H, Kawaoto, H, Watanabe, T, Itoh, N, Ishiwatari, T, Koeda
Publikováno v:
The Japanese journal of antibiotics. 37(7)
Miokamycin (MOM) is a derivative of midecamycin, a macrolide antibiotic isolated from a culture broth of Streptomyces mycarofaciens. The objective of this study was to determine the chronic toxicity of MOM in male and female rats (Wistar, SPF, 5-week
Autor:
M, Yokota, U, Takeda, M, Odaki, H, Sasaki, T, Niizato, H, Kawaoto, H, Watanabe, N, Ishiwatari, H, Hayasaka, T, Koeda
Publikováno v:
The Japanese journal of antibiotics. 37(8)
Miocamycin (MOM) is a derivative of midecamycin and is metabolized into 4 main metabolites of Mb1, Mb2, Mb6 and Mb12. In the previous study, LD0 values of Mb12 in male and female rats were estimated more than 5,000 mg/kg. The object of this study was
Autor:
R W, James, P F, Wadsworth, H, Chesterman, S A, Ball, S K, Majeed, R, Heywood, A E, Street, T, Koeda, U, Takeda, H, Sasaki
Publikováno v:
The Japanese journal of antibiotics. 33(8)
Dibekacin sulphate (DKB), a new aminoglycoside antibiotic developed on the theory of bacterial resistance, was given by intravenous injection to groups of female Beagle dogs at dosages of 2.5, 5.0, 10.0 or 25.0 mg/kg/day for 13 weeks. Physiological s
Publikováno v:
The Japanese journal of antibiotics. 37(8)
We evaluated acute toxicity and estimated LD50 values of Mb12, one of the main metabolites of MOM, in male and female mice after single oral administration. Observations were continued for 1 week after treatment. The LD50 values were calculated accor