Zobrazeno 1 - 10
of 32
pro vyhledávání: '"John G, Page"'
Publikováno v:
Basic & Clinical Pharmacology & Toxicology. 106:511-522
4-[3-(2-Nitro-1-imidazolyl)-propylamino]-7-chloroquinoline hydrochloride (NLCQ-1), a 2-nitroimidazole-based hypoxia-selective cytotoxin has been shown to target hypoxic regions of solid tumours. The present study is one of several pre-clinical toxico
Publikováno v:
Basic & Clinical Pharmacology & Toxicology. 106:497-504
In pre-clinical studies, 4-[3-(2-nitro-1-imidazolyl)-propylamino]-7-chloroquinoline hydrochloride (NLCQ-1, NSC 709257) is a weak DNA-intercalating, hypoxia-selective cytotoxin with a promising profile as an adjuvant to radio/chemotherapy and it is ab
Autor:
Karen Schweikart, John G. Page, Patricia E. Noker, David H. Munn, Joel M. Reid, Sarah A. Buhrow, Joseph E. Tomaszewski, Lee Jia, Matthew M. Ames
Publikováno v:
Food and Chemical Toxicology. 46:203-211
1-methyl-d-tryptophan (D-1MT) reverses the immunosuppressive effect of indoleamine 2,3-dioxygenase (IDO), and it is currently being developed both as a vaccine adjuvant and as an immunotherapeutic agent for combination with chemotherapy. The present
Publikováno v:
Toxicology and Applied Pharmacology. 211:115-123
Indole-3-carbinol (I-3-C) and 3,3'-diindolylmethane (DIM) have been shown to reduce the incidence and multiplicity of cancers in laboratory animal models. Based on the observation that I-3-C induced hepatocyte hypertrophy when administered orally for
Autor:
Katsumi Kurokawa, Shin J. Oh, Charles D. Hébert, Yun Zhang, Karen Schweikart, John G. Page, Diogo Fraxino de Almeida
Publikováno v:
Clinical Neurophysiology. 115:1677-1682
Objective In rats the available techniques for evaluation of sensory nerve conduction are limited. We report a new method of sensory nerve conduction of the plantar nerve using needle electrodes as the recording electrodes behind the medial malleolus
Publikováno v:
The Journal of Clinical Pharmacology. 38:166-171
A 56-day pharmacokinetic study of zonisamide was conducted in 24 healthy volunteers. Steady state was achieved in 29 days including two dose escalations, and in an average of 15 days from the last dose adjustment. Twice-daily administration of 200 mg
Autor:
Joseph E. Tomaszewski, Martin J. Murphy, Richard D. May, Blaire Osborn, Connie L. Erickson-Miller, Ralph E. Parchment, John G. Page
Publikováno v:
Cancer Chemotherapy and Pharmacology. 39:467-472
Purpose: 20(S)-Camptothecin (CAM), topotecan (TPT, active ingredient in Hycamtin) and 9-amino-20(S)-camptothecin (9AC) are topoisomerase I inhibitors that cause similar dose-limiting toxicities to rapidly renewing tissues, such as hematopoietic tissu
Autor:
JAMES A. CROWELL, JOHN G. PAGE, LARRY E. RODMAN, JAMES E. HEATH, EDWIN I. GOLDENTHAL, LEROY B. HALL, GARY J. KELLOFF
Publikováno v:
Toxicological Sciences. 35:9-21
Publikováno v:
Annals of the New York Academy of Sciences. 801:205-216
Acute administration of high doses of ibogaine (IBG) to the male rat results in degeneration of Purkinje cells and reactive gliosis in the cerebellar vermis. We examined whether acute and chronic administration of IBG to male and female rats results
Publikováno v:
Basicclinical pharmacologytoxicology. 106(6)
4-[3-(2-Nitro-1-imidazolyl)-propylamino]-7-chloroquinoline hydrochloride (NLCQ-1), a 2-nitroimidazole-based hypoxia-selective cytotoxin has been shown to target hypoxic regions of solid tumours. The present study is one of several pre-clinical toxico