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Hansen Bow

Researcher at Vanderbilt University Medical Center

Publications -  30
Citations -  1328

Hansen Bow is an academic researcher from Vanderbilt University Medical Center. The author has contributed to research in topics: Temozolomide & Population. The author has an hindex of 12, co-authored 29 publications receiving 1179 citations. Previous affiliations of Hansen Bow include Johns Hopkins University & Johns Hopkins University School of Medicine.

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Microfluidics for cell separation.

TL;DR: This review describes the current state-of-the-art in microfluidics-based cell separation techniques, and common separation metrics, including separation markers, resolution, efficiency, and throughput, of these techniques are discussed.
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A microfabricated deformability-based flow cytometer with application to malaria

TL;DR: An automated microfabricated "deformability cytometer" is introduced that measures dynamic mechanical responses of 10(3) to 10(4) individual RBCs in a cell population, resulting in a population-based correlation between biochemical properties, such as cell surface markers, and dynamic mechanical deformability.
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Pf155/RESA protein influences the dynamic microcirculatory behavior of ring-stage Plasmodium falciparum infected red blood cells

TL;DR: This is the first identification of a parasite factor influencing the dynamic circulation of young asexual Pf-RBCs in physiologically relevant conditions, offering novel possibilities for interventions to reduce parasite survival and pathogenesis in its human host.
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Intracranial MEMS based temozolomide delivery in a 9L rat gliosarcoma model.

TL;DR: Results from the in vivo efficacy studies indicate that early, rapid delivery of TMZ from the device results in the most prolonged animal survival, and the ability to actively control the rate and timing of drug release holds tremendous potential for the treatment of BTs and related diseases.

Dynamic deformability of Plasmodium falciparum-infected erythrocytes exposed to artesunate in vitro

TL;DR: It is demonstrated, for the first time, that ART reduces the dynamic and quasi-static RBC deformability, which may subsequently influence blood circulation through the microvasculature and spleen cordal meshwork, thus adding a new aspect to artesunate's mechanism of action.