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Barry Kiely

Researcher at University College Cork

Publications -  97
Citations -  9442

Barry Kiely is an academic researcher from University College Cork. The author has contributed to research in topics: Probiotic & Bifidobacterium. The author has an hindex of 34, co-authored 97 publications receiving 8546 citations. Previous affiliations of Barry Kiely include Procter & Gamble & National University of Ireland.

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Lactobacillus and bifidobacterium in irritable bowel syndrome: Symptom responses and relationship to cytokine profiles

TL;DR: B infantis 35624 alleviates symptoms in IBS; this symptomatic response was associated with normalization of the ratio of an anti-inflammatory to a proinflammatory cytokine, suggesting an immune-modulating role for this organism, in this disorder.
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In vitro selection criteria for probiotic bacteria of human origin: correlation with in vivo findings

TL;DR: Criteria for in vitro selection of probiotic bacteria that may reflect certain in vivo effects on the host such as modulation of gastrointestinal tract microflora is developed.
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Effects of the probiotic Bifidobacterium infantis in the maternal separation model of depression.

TL;DR: Findings point to a more influential role for bifidobacteria in neural function, and suggest that probiotics may have broader therapeutic applications than previously considered.
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Efficacy of an encapsulated probiotic Bifidobacterium infantis 35624 in women with irritable bowel syndrome.

TL;DR: B. infantis 35624 at a dose of 1 × 108 cfu was significantly superior to placebo and all other bifidobacterium doses for the primary efficacy variable of abdominal pain as well as the composite score and scores for bloating, bowel dysfunction, incomplete evacuation, straining, and the passage of gas at the end of the 4-wk study.
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Double blind, placebo controlled trial of two probiotic strains in interleukin 10 knockout mice and mechanistic link with cytokine balance

TL;DR: Both Lactobacillus salivarius and Bifidobacterium infantis 35624 significantly attenuate colitis in this murine model, associated with a reduced ability to produce Th1-type cytokines systemically and mucosally while levels of TGF-β are maintained.