Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Haig P. Bozigian"'
Autor:
Nicole D, Harriott, John P, Williams, Evan B, Smith, Haig P, Bozigian, Dimitri E, Grigoriadis
Publikováno v:
Progress in medicinal chemistry. 57(1)
The dopaminergic system plays a key role in the central nervous system, regulating executive function, arousal, reward, and motor control. Dysregulation of this critical monoaminergic system has been associated with diseases of the central nervous sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0bd6a8061f48be128165ea005bfbc385
https://pubmed.ncbi.nlm.nih.gov/29680151
https://pubmed.ncbi.nlm.nih.gov/29680151
Autor:
Robert L. Hall, Haig P. Bozigian, Lorrene Buckley Kedderis, Steadman D. Harrison, Robert L. Susick, James M. Kleeman, Thomas E. Palmer
Publikováno v:
Fundamental and Applied Toxicology. 25:201-217
Toxicity of the Protein Kinase C Inhibitor Safingol Administered Alone and in Combination with Chemotherapeutic Agents. Kedderis, L. B., Bozigian, H. P., Kleeman, J. M., Hall, R. L., Palmer, T. E., Harrison, S. D., Jr., and Susick, R. L., Jr. (1995).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6abb6f4f0c8326d89732e121c674194f
https://doi.org/10.1006/faat.1995.1056
https://doi.org/10.1006/faat.1995.1056
Autor:
Toni Bjurstrom, Ann E. Gooding, Rita H. Griffin, Rodney Mitchell, Haig P. Bozigian, Timothy L. Panella, J. Frederick Pritchard, Andrew T. Huang, Poe‐Hirr Hsyu, Lea Ann Hansen
Publikováno v:
Journal of clinical pharmacology. 34(7)
The effect of a typical 5-day chemotherapy treatment with cisplatin (20-40 mg/m2 per day) and 5-fluorouracil (5-FU, 1 gm/m2 per day) on the pharmacokinetics of ondansetron was investigated. Twenty cancer patients received 8 mg of ondansetron in three
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aac458d932a1231ebbec81246bf30622
https://pubmed.ncbi.nlm.nih.gov/7929872
https://pubmed.ncbi.nlm.nih.gov/7929872
Publikováno v:
DICP : the annals of pharmacotherapy. 24(11)
Virtually all patients who are under the physiologic stress of an intensive care unit (ICU) are vulnerable to stress-related mucosal damage and ulceration. Although clinically significant hemorrhage from stress ulceration occurs in only 5-20 percent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeb65bab0e84c32b22ffbb58794bb00c
https://pubmed.ncbi.nlm.nih.gov/2275223
https://pubmed.ncbi.nlm.nih.gov/2275223
Publikováno v:
Toxicology and Applied Pharmacology. 71:353-361
A circadian rhythm in the toxicity of acetaminophen administered at different times of the day was exhibited in male mice. Peak lethality (70% dead) occurred at 1800 hr and nadir lethality (10% dead) occurred at 1000 hr. Hepatic nonprotein sulfhydryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dff6577c61b226b2baeb6677089ec0a
https://doi.org/10.1016/0041-008x(83)90022-4
https://doi.org/10.1016/0041-008x(83)90022-4
Circadian variations in glutathione-S-transferase and glutathione peroxidase activities in the mouse
Publikováno v:
Toxicology letters. 19(1-2)
Circadian variations in hepatic glutathione-S-transferase and glutathione peroxidase activities were found in male Swiss-Webster mice maintained under a 12/12 lighting schedule (L: 06.00-18.00 h) for 3 weeks prior to use. Hepatic glutathione-S-transf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40cc06a325e61b132bd966bc370254db
https://pubmed.ncbi.nlm.nih.gov/6658827
https://pubmed.ncbi.nlm.nih.gov/6658827
Publikováno v:
Pharmacology. 29(3)
Experiments were conducted to examine the effects of changes in lighting schedules and food consumption on circadian rhythms in acetaminophen lethality and hepatic glutathione levels in male mice. Under a normal lighting schedule (light: 06.00–18.0
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c58e1295b1dc167e490c5bd9823b6c2
https://pubmed.ncbi.nlm.nih.gov/6483961
https://pubmed.ncbi.nlm.nih.gov/6483961