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Thomas M. Badger

Researcher at University of Arkansas for Medical Sciences

Publications -  305
Citations -  13313

Thomas M. Badger is an academic researcher from University of Arkansas for Medical Sciences. The author has contributed to research in topics: Soy protein & Offspring. The author has an hindex of 63, co-authored 299 publications receiving 12304 citations. Previous affiliations of Thomas M. Badger include University of Arkansas & United States Department of Agriculture.

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Gonadal Steroid Modulation of Growth Hormone Secretory Patterns in the Rat

TL;DR: Growth hormone secretory patterns are governed principally by two peptides, somatostatin and growth hormone-releasing factor, whose centers are located within the medial preoptic/anterior periventricular and the ventromedial/arcuate region of the hypothalamus.
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Air displacement plethysmography, dual-energy X-ray absorptiometry, and total body water to evaluate body composition in preschool-age children.

TL;DR: D(2)O, DXA, or quantitative nuclear magnetic resonance may be considered better options for assessing fat mass in young children when compared with ADP, which does not accurately assess percentFat mass in children aged 3 to 5 years.
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In vitro actions on human cancer cells and the liquid chromatography-mass spectrometry/mass spectrometry fingerprint of phytochemicals in rice protein isolate

TL;DR: In vitro antitumor activities of an ether fraction from RPI was studied using human tumor cell lines, including two human breast carcinoma cell lines (MDA-MB-453 and MCF-7) and two myeloma cell Lines (RPMI-8226 and IM-9).
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Effects of light and dark beer on hepatic cytochrome P-450 expression in male rats receiving alcoholic beverages as part of total enteral nutrition.

TL;DR: Stochastic microsomes from stout-infused rats had greater hepatic microsomal erythromycin N-demethylase activity than other groups, and Stout contains components other than ethanol that interact in a complex fashion with the monooxygenase system.
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Soy protein isolate induces CYP3A1 and CYP3A2 in prepubertal rats.

TL;DR: It is suggested that early soy consumption may increase the metabolism of a wide variety of CYP3A substrates, but that soy does not imprint the expression of CYp3A enzymes.