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Wendy R. Russell
Researcher at University of Aberdeen
Publications - 91
Citations - 4609
Wendy R. Russell is an academic researcher from University of Aberdeen. The author has contributed to research in topics: Postprandial & Chemistry. The author has an hindex of 31, co-authored 82 publications receiving 3621 citations. Previous affiliations of Wendy R. Russell include Rowett Research Institute.
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Journal ArticleDOI
High-protein, reduced-carbohydrate weight-loss diets promote metabolite profiles likely to be detrimental to colonic health
Wendy R. Russell,Silvia W. Gratz,Sylvia H. Duncan,Grietje Holtrop,Jennifer Ince,Lorraine Scobbie,Garry Duncan,Alexandra M. Johnstone,Gerald E. Lobley,R. John Wallace,Garry G. Duthie,Harry J. Flint +11 more
TL;DR: Weight-loss diets that were high in protein but reduced in total carbohydrates and fiber resulted in a significant decrease in fecal cancer-protective metabolites and increased concentrations of hazardous metabolites, which may increase risk of colonic disease.
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Low-grade inflammation, diet composition and health: current research evidence and its translation
Anne Marie Minihane,Sophie Vinoy,Wendy R. Russell,Athanasia Baka,Helen M. Roche,Kieran Tuohy,Jessica L. Teeling,Ellen E. Blaak,Michael Fenech,David Vauzour,Harry J. McArdle,Bas Kremer,Luc Sterkman,Katerina Vafeiadou,M. Massi Benedetti,Christine M. Williams,Philip C. Calder +16 more
TL;DR: The present position paper is the most recent in a series produced by the International Life Sciences Institute's European Branch and is co-authored by the speakers from a 2013 workshop led by the Obesity and Diabetes Task Force entitled ‘Low-grade inflammation, a high-grade challenge: biomarkers and modulation by dietary strategies’.
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Colonic bacterial metabolites and human health
TL;DR: The role of the gut microbiota in choline deficiency in non-alcoholic fatty liver disease (NAFLD) and insulin resistance is receiving increased attention, and the 'gut-liver axis' is an emerging area of study.
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Major phenylpropanoid‐derived metabolites in the human gut can arise from microbial fermentation of protein
Wendy R. Russell,Sylvia H. Duncan,Lorraine Scobbie,Gary Duncan,Louise Cantlay,A. Graham Calder,Susan E. Anderson,Harry J. Flint +7 more
TL;DR: This study demonstrates that certain microbial species have the ability to ferment all three AAAs and that protein fermentation is the likely source of major phenylpropanoid-derived metabolites in the colon.
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Potential of Fava Bean as Future Protein Supply to Partially Replace Meat Intake in the Human Diet
TL;DR: The potential of fava bean as a functional food ingredient to partially replace meat in the human diet and can provide a more environmentally friendly substitution for industrial N-fertilizers with associated improvements in resource efficiency and production costs is focused on.