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A.M. Monro
Researcher at Pfizer
Publications - 37
Citations - 2263
A.M. Monro is an academic researcher from Pfizer. The author has contributed to research in topics: Toxicity & Pharmacokinetics. The author has an hindex of 15, co-authored 37 publications receiving 2095 citations.
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Journal ArticleDOI
Concordance of the toxicity of pharmaceuticals in humans and in animals.
Harry Olson,Graham Betton,Denise Robinson,Karluss Thomas,A.M. Monro,Gerald Kolaja,Patrick D. Lilly,James E. Sanders,Glenn Sipes,William Bracken,Michael A. Dorato,Koen Van Deun,Peter Smith,Bruce Berger,Allen H. Heller +14 more
TL;DR: The survey results support the value of in vivo toxicology studies to predict for many significant HTs associated with pharmaceuticals and have helped to identify HT categories that may benefit from improved methods.
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Marketed Human Pharmaceuticals Reported to be Tumorigenic in Rodents
Thomas S. Davies,A.M. Monro +1 more
TL;DR: The 1994 U.S. Physicians' Desk Reference reports the results of rodent carcinogenicity tests on 241 pharmaceutical agents, with a class label implying a carcinogenic hazard also attached to 9 estrogenic, 4 androgenic, and 3 progestogenic agents.
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Effects of housing conditions on food intake, body weight and spontaneous lesions in mice. A review of the literature and results of an 18-month study.
TL;DR: The more densely housed groups showed markedly reduced food consumption, slightly decreased mean body weights, and a smaller variance of body weights.
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Hepatic Foci of Cellular and Enzymatic Alteration and Nodules in Rats Treated With Clofibrate or Diethylnitrosamine Followed by Phenobarbital: Their Rate of Onset and Their Reversibility
TL;DR: The histologic appearance and cytochemical characteristics of foci of hepatic cellular alteration, hepatic nodules, and hepatocellular carcinomas occurring in male Sprague-Dawley rats treated with the hypolipidemic agent clofibrate, with phenobarbital, or with diethylnitrosamine followed by phenobarBital were studied after treatment periods from 1 month to 2 years.
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What is an appropriate measure of exposure when testing drugs for carcinogenicity in rodents
TL;DR: It is argued that in the carcinogenicity testing of drugs, biological measures of drug exposure may often be more relevant than the classical pharmacokinetic approaches applicable to reversible pharmacodynamic phenomena.