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M

Martina M. Prendergast

Researcher at National University of Ireland, Galway

Publications -  19
Citations -  1937

Martina M. Prendergast is an academic researcher from National University of Ireland, Galway. The author has contributed to research in topics: Campylobacter jejuni & Molecular mimicry. The author has an hindex of 18, co-authored 19 publications receiving 1774 citations.

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Silver nanoparticles in the environment: Sources, detection and ecotoxicology.

TL;DR: The overall aim of this review is to examine methods for the capture and detection of AgNPs, potential toxicity and transmission routes in the aquatic environment.
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Molecular mimicry of host structures by bacterial lipopolysaccharides and its contribution to disease

TL;DR: The core oligosaccharides of low-molecular-weight lipopolysaccharide (LPS) of pathogenic Neisseria spp.
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Phase Variation of Campylobacter jejuni 81-176 Lipooligosaccharide Affects Ganglioside Mimicry and Invasiveness In Vitro

TL;DR: Genetic analyses of genes involved in the biosynthesis of the outer core of C. jejuni 81-176 revealed the presence of a homopolymeric tract of G residues within a gene encoding CgtA, an N-acetylgalactosaminyltransferase that corresponded to a change in LOS structure from GM2 to GM3 ganglioside mimicry.
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Sialylation of Lipooligosaccharide Cores Affects Immunogenicity and Serum Resistance of Campylobacter jejuni

TL;DR: Mutation of genes encoding proteins with homology to a sialyl transferase (cstII) and a putative N-acetylmannosamine synthetase (neuC1) resulted in LOS cores intermediate in electrophoretic mobility between that of wild type and the mutants lacking NeuNAc, loss of reactivity with CT, and a reduced immunoreactivity with hyperimmune antiserum.
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Lipopolysaccharides from Campylobacter jejuni O:41 strains associated with Guillain-Barré syndrome exhibit mimicry of GM1 ganglioside.

TL;DR: The aim of the study was to determine the structure of the core oligosaccharide of the lipopolysaccharide (LPS) of C. jejuni serotype O:41, a serotype rarely associated with the development of GBS, and to determine if the LPS shares similar epitopes with any of the major human gangliosides.