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Tineke Schollaardt

Researcher at University of Calgary

Publications -  6
Citations -  725

Tineke Schollaardt is an academic researcher from University of Calgary. The author has contributed to research in topics: Cell adhesion molecule & Cytokine. The author has an hindex of 5, co-authored 6 publications receiving 688 citations. Previous affiliations of Tineke Schollaardt include Mahidol University.

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The Prognostic and Pathophysiologic Role of Pro- and Antiinflammatory Cytokines in Severe Malaria

TL;DR: Elevated plasma cytokines in severe malaria are associated with systemic pathologic abnormalities, not cerebral involvement, and both the overall magnitude of the cytokine responses and the eventual imbalance between the pro- and antiinflammatory responses are important determinants of mortality.
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Synergism of multiple adhesion molecules in mediating cytoadherence of Plasmodium falciparum–infected erythrocytes to microvascular endothelial cells under flow

TL;DR: Findings indicate that IRBCs interact synergistically with multiple adhesion molecules on vascular endothelium, since it can be modulated by cytokines to enhance CD36-mediated IRBC adhesion.
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Endogenous interleukin-10 modulates proinflammatory response in Plasmodium falciparum malaria.

TL;DR: Findings suggest that IL-10 counter-regulates the proinflammatory response to P. falciparum malaria, which may be associated with an inadequate negative feedback response byIL-10.
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Characterization of Plasmodium falciparum -Infected Erythrocyte and P-Selectin Interaction Under Flow Conditions

TL;DR: Investigation of the molecular interactions between IRBC and P-selectin using a laminar flow system showed that cytoadherence under physiological flow conditions may be mediated by multiple IRBC ligands that interact with different adhesion molecules in a cooperative fashion.
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Efficacy of oral immunization with Pseudomonas aeruginosa lipopolysaccharide

TL;DR: Protection against P. aeruginosa in an ironloaded mouse model and a burned mouse model of infection was achieved and passive transfer experiments demonstrated that protection was associated with specific antibody and not by cell mediated immunity.