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Catherine Stanton

Researcher at Teagasc

Publications -  592
Citations -  52749

Catherine Stanton is an academic researcher from Teagasc. The author has contributed to research in topics: Gut flora & Microbiome. The author has an hindex of 98, co-authored 540 publications receiving 40765 citations. Previous affiliations of Catherine Stanton include National University of Ireland & University College Cork.

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The effects of conditioning on meat collagen: Part 1-Evidence for gross in situ proteolysis.

TL;DR: SDS- and urea-washing were showd to yield clean connective tissue preparations and to extract the largest quantities of soluble collagen from perimysial preparations and it was not possible to demonstrate similar changes in endomysIAL preparations due to the difficulty in quantitating the relatively low amounts of collagen in these fractions.
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Feeding melancholic microbes: MyNewGut recommendations on diet and mood.

TL;DR: Patients with depression or vulnerability to depression should be encouraged to enhance a plant-based diet with a high content of grains/fibres and fish, the MyNewGut consortium recommends.
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Use of viability staining in combination with flow cytometry for rapid viability assessment of Lactobacillus rhamnosus GG in complex protein matrices

TL;DR: This methodology provides impetus for dynamic progression of FACS for rapid viability assessment of live bacteria immobilized/encapsulated within complex protein systems.
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Sources and Bioactive Properties of Conjugated Dietary Fatty Acids.

TL;DR: This review highlights the common sources of these conjugated fatty acids, including plants, algae, microbes and chemosynthesis, and suggests these fatty acids may play a role in modulating the expression of several oncogenes, cell cycle regulators, and genes associated with energy metabolism.
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Identification of aminoglycoside and β-lactam resistance genes from within an infant gut functional metagenomic library

TL;DR: Insight is provided into the infant gut resistome, revealing the presence of a varied aminoglycoside and β-lactam resistance reservoir even in the absence of selective pressure, confirming the infant resistome establishes early in life, perhaps even at birth.