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Russell J. Mumper

Researcher at University of North Carolina at Chapel Hill

Publications -  155
Citations -  16694

Russell J. Mumper is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Antigen & Drug carrier. The author has an hindex of 57, co-authored 154 publications receiving 14885 citations. Previous affiliations of Russell J. Mumper include University of Kentucky & University of Georgia.

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Plant phenolics: extraction, analysis and their antioxidant and anticancer properties.

Jin Dai, +1 more
- 21 Oct 2010 - 
TL;DR: The anticancer effects of phenolics in-vitro and in- vivo animal models are viewed, including recent human intervention studies, and possible mechanisms of action involving antioxidant and pro-oxidant activity as well as interference with cellular functions are discussed.
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The Flipped Classroom: A Course Redesign to Foster Learning and Engagement in a Health Professions School

TL;DR: The authors describe the philosophy and methodology used to redesign the Basic Pharmaceutics II course and outline the research they conducted to investigate the resulting outcomes, concluding that this approach warrants careful consideration as educators aim to enhance learning, improve outcomes, and fully equip students to address 21st-century health care needs.
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Elevated copper and oxidative stress in cancer cells as a target for cancer treatment

TL;DR: This review discusses the targeting of the elevated copper levels and oxidative stress levels in cancer with the aid of a copper chelator d-penicillamine (d-pen) for potential cancer treatment.
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Nanoparticle Surface Charges Alter Blood–Brain Barrier Integrity and Permeability

TL;DR: In this article, the effect of neutral, anionic and cationic charged nanoparticles on the blood-brain barrier (BBB) and brain permeability was evaluated by in situ rat brain perfusion.
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Chitosan and depolymerized chitosan oligomers as condensing carriers for in vivo plasmid delivery

TL;DR: The combination of strong complex stability and low in vivo expression levels suggest that uptake and/or decomplexation, but not endosomal release, may be the critical rate-limiting steps in the uptake process.