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Fergus Shanahan

Researcher at National University of Ireland

Publications -  727
Citations -  59181

Fergus Shanahan is an academic researcher from National University of Ireland. The author has contributed to research in topics: Inflammatory bowel disease & Gut flora. The author has an hindex of 117, co-authored 705 publications receiving 51963 citations. Previous affiliations of Fergus Shanahan include Imperial College London & Mater Misericordiae Hospital.

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Medical treatment of inflammatory bowel disease.

TL;DR: Advances in the drug treatment of inflammatory bowel disease include the development of site-specific delivery systems for 5-aminosalicylate, topically active corticosteroids with minimal systemic bioavailability, and a variety of antagonists to specific inflammatory mediators.
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Pharmabiotic manipulation of the microbiota in gastrointestinal disorders, from rationale to reality.

TL;DR: Clinicians should adhere to the principles of evidence-based therapeutics in choosing a probiotic strategy, including: selection from a reputable supplier, with appropriate documentation of contents and shelf life; anticipation of strain-specific effects; avoidance of cocktails without documentation of the activities of each ingredient with absence of interstrain antagonism.
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Bifidobacterium infantis 35624 protects against salmonella-induced reductions in digestive enzyme activity in mice by attenuation of the host inflammatory response.

TL;DR: Salmonella infection reduces the small intestinal brush border enzyme activity in mice, with the level of reduction and associated weight loss increasing with dose and duration of infection.
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Mucosal subepithelial binding sites for the bacterial chemotactic peptide, formyl-methionyl-leucyl-phenylalanine (FMLP)

TL;DR: Receptors for FMLP are subepithelial and map to the lamina propria of the gastrointestinal mucosa and are detected in activated peripheral blood phagocytes and epithelial cell lines.
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Fas ligand promotes tumor immune evasion of colon cancer in vivo.

TL;DR: It is indicated that upregulation of FasL expression by colon tumor cells results in an improved anti-tumor immune challenge in vivo, providing functional evidence in favor of the ‘Fas counterattack’ as a mechanism of tumor immune evasion.