J
James M. Perel
Researcher at New York University
Publications - 5
Citations - 134
James M. Perel is an academic researcher from New York University. The author has contributed to research in topics: Ascorbic acid & Excretion. The author has an hindex of 5, co-authored 5 publications receiving 134 citations. Previous affiliations of James M. Perel include Columbia University.
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A study of structure-activity relationships in regard to species difference in the phenylbutazone series
TL;DR: Physicochemical properties of phenylbutazone analogues were correlated with their physiological disposition, in particular with reference to species difference, while in man there exists a direct relationship between pKa and half-life, no such correlation was observed in dogs.
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The relationship between binding of thiopental to plasma and its distribution into adipose tissue in man, as measured by a spectrophotofluorometric method
Peter G. Dayton,Peter G. Dayton,James M. Perel,James M. Perel,Miguel A. Landrau,Miguel A. Landrau,Leonard Brand,Leonard Brand,Lester C. Mark,Lester C. Mark +9 more
TL;DR: Binding in vitro of thiopental to human plasma was measured by a spectrophotofluorometric method as well as by radioactive procedures, and specificity has been proven by a quantitative thin-layer Chromatographie technique.
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Ascorbic and dehydroascorbic acids in guinea pigs and rats.
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Thiopental Metabolism by Human Liver in vivo and in vtro
Lester C. Mark,Leonard Brand,Sonia Kamvyssi,Richard C. Britton,James M. Perel,Miguel A. Landrau,Peter G. Dayton +6 more
TL;DR: This work has shown that the life time of the most labile component in nuclear RNA is estimated to be 20-30 min, and this work aims to extend this estimate to include the half-life of messenger RNA.
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Studies of the prolonged biochemical effects of 3-methylcholanthrene and of its physiological disposition in the rat.
TL;DR: It was found that in the initial 24 hr following administration, Chloretone produced a marked increase in ascorbic acid excretion and a moderate rise of zoxazolamine hydroxylase activity, which suggests that these two biochemical responses may not be interrelated.