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Nina Wale

Researcher at University of Michigan

Publications -  15
Citations -  266

Nina Wale is an academic researcher from University of Michigan. The author has contributed to research in topics: Drug resistance & Competition (biology). The author has an hindex of 6, co-authored 14 publications receiving 222 citations. Previous affiliations of Nina Wale include Michigan State University & Pennsylvania State University.

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Resource limitation prevents the emergence of drug resistance by intensifying within-host competition

TL;DR: This work shows that the emergence of drug resistance can be prevented by reducing the availability of a nutrient for which drug-resistant parasites are especially hungry, and provides proof of principle that chemotherapy paired with an “ecological” intervention can slow the evolution of resistance to antimicrobial drugs, even when resistant pathogens are present at high frequencies.
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A nutrient mediates intraspecific competition between rodent malaria parasites in vivo

TL;DR: It is demonstrated that a parasite nutrient, para-aminobenzoic acid (pABA), mediates competition between a drug resistant and drug susceptible strain of the malaria parasite, Plasmodium chabaudi, and that increasing pABA supply to hosts infected with the resistant strain worsens disease and changes the relationship between parasite burden and pathology.
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Model Systems in Ecology, Evolution, and Behavior: A Call for Diversity in Our Model Systems and Discipline*

TL;DR: This introduction to the Special Feature on Model Systems in Ecology, Evolution, and Behavior (EEB), grappling with the question, What is a model system is begun, and the importance of communities of scientists in the success of model systems is emphasized—narrow scientific communities can restrict the model organisms themselves.
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The contribution of host cell-directed vs. parasite-directed immunity to the disease and dynamics of malaria infections.

TL;DR: It is found that hosts control infections not only by killing pathogens, but by starving parasites and shortening the lifespans of cells on which they depend, revealing that some immune responses seen as harmful to the host may in fact be helpful and suggesting simple rules that govern the immune response’s deployment.