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Matthew A. Wallig

Researcher at University of Illinois at Urbana–Champaign

Publications -  115
Citations -  4153

Matthew A. Wallig is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Mammary tumor & Pancreatitis. The author has an hindex of 33, co-authored 115 publications receiving 3785 citations. Previous affiliations of Matthew A. Wallig include Urbana University.

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BookDOI

Haschek and Rousseaux's handbook of toxicologic pathology

TL;DR: The 3e has been expanded by a full volume, and covers aspects of safety assessment not discussed in the 2e, and provides new chapters and in-depth discussion of timely topics in the area of toxicologic pathology.
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A high protein moderate carbohydrate diet fed at discrete meals reduces early progression of N-methyl-N-nitrosourea-induced breast tumorigenesis in rats.

TL;DR: Evidence is provided that reducing the dietary carbohydrate:protein ratio attenuates the development of mammary tumors and is consistent with reduced post-prandial insulin release potentially diminishing the proliferative environment required for breast cancer tumors to progress.
Journal ArticleDOI

Inhibition by rosemary and carnosol of 7,12-dimethylbenz[a]anthracene (DMBA)-induced rat mammary tumorigenesis and in vivo DMBA-DNA adduct formation

TL;DR: Carnosol is one rosemary constituent that can prevent DMBA-induced DNA damage and tumor formation in the rat mammary gland, and, thus, has potential for use as a breast cancer chemopreventative agent.
Journal ArticleDOI

Dietary fructose induces a wide range of genes with distinct shift in carbohydrate and lipid metabolism in fed and fasted rat liver

TL;DR: Fructose feeding induced a broader range of genes than previously identified with simultaneous increase in glycogen and triglycerides in liver, and may be in part mediated by ChREBP.
Journal ArticleDOI

Inorganic delivery vector for intravenous injection.

TL;DR: In vivo testing of empty LDH administered to adult male Sprague Dawley rats was done to evaluate the possibility of using LDH as an injectable drug delivery vehicle.