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Weam I. Zaky

Researcher at Smith College

Publications -  7
Citations -  143

Weam I. Zaky is an academic researcher from Smith College. The author has contributed to research in topics: Brugia malayi & Ecdysone receptor. The author has an hindex of 6, co-authored 7 publications receiving 114 citations. Previous affiliations of Weam I. Zaky include Northampton Community College.

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Journal ArticleDOI

A Novel Xenomonitoring Technique Using Mosquito Excreta/Feces for the Detection of Filarial Parasites and Malaria.

TL;DR: The new method presented here screens the excreta/feces from hundreds of mosquitoes per pool and provides proof-of-concept for a practical alternative to traditional methodologies resulting in significant cost and labor savings, and has the potential to greatly reduce MX costs.
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The Effect of In Vitro Cultivation on the Transcriptome of Adult Brugia malayi

TL;DR: These findings suggest that B. malayi can be maintained in culture as a valid system for pharmacological and biological studies, at least for several days after removal from the host and adaptation to the new environment.
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The Effects of Ivermectin on Brugia malayi Females In Vitro: A Transcriptomic Approach.

TL;DR: It is hypothesized that paralysis of pharyngeal pumping by ivermectin in filariae could result in deprivation of essential nutrients, especially iron, inducing a wide range of responses evidenced by altered gene expression, changes in metabolic pathways, and altered developmental states in embryos.
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Backpack PCR: A Point-of-Collection Diagnostic Platform for the Rapid Detection of Brugia Parasites in Mosquitoes

TL;DR: This point-of-collection diagnostic platform provides an alternative to cost-prohibitive column-dependent DNA extractions that are typically coupled to detection methodologies requiring advanced laboratory infrastructure and should increase the feasibility of molecular xenomonitoring within B. malayi-endemic locations.
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Profiling the macrofilaricidal effects of flubendazole on adult female Brugia malayi using RNAseq.

TL;DR: Drug effects assessed using a transcriptomic approach support the hypothesis that FLBZ acts predominantly on rapidly dividing cells, and provides a basis for selecting molecular markers of drug-induced damage which may be of use in predicting efficaciousFLBZ regimens.