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Mehmet Toner

Researcher at Harvard University

Publications -  572
Citations -  60830

Mehmet Toner is an academic researcher from Harvard University. The author has contributed to research in topics: Circulating tumor cell & Cancer. The author has an hindex of 113, co-authored 550 publications receiving 54827 citations. Previous affiliations of Mehmet Toner include University of New Mexico & University of Notre Dame.

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Microfabrication of hepatocyte/fibroblast co-cultures: role of homotypic cell interactions.

TL;DR: The data suggest that fibroblast number plays a role in modulation of hepatocellular response through homotypic fibro Blast interactions, and this approach will allow further elucidation of the complex interplay between two cell types as they form a functional model tissue in vitro or as they interact in vivo to form afunctional organ.
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Cellular micropatterns on biocompatible materials.

TL;DR: Micropatterns of collagen or fibronectin were used to selectively adhere cells on various biomedical polymers and on heterogeneous or microtextured substrates to provide inexpensive patterning of a rich assortment of biomolecules, cells, and surfaces under physiological conditions.
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Androgen Receptor Signaling in Circulating Tumor Cells as a Marker of Hormonally Responsive Prostate Cancer

TL;DR: Microfluidic capture of circulating tumor cells (CTC) is used to measure AR signaling readouts before and after therapeutic interventions to help target treatments to patients most likely to respond to second-line therapies.
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Surface engineering with poly(ethylene glycol) photolithography to create high-density cell arrays on glass

TL;DR: This manuscript presents a microfabrication-derived approach for controlling mammalian cell−surface interactions by patterning high-density arrays of micrometer-scale PEG hydrogel wells on glass to induce hepatocyte attachment.
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Liver-specific functional studies in a microfluidic array of primary mammalian hepatocytes.

TL;DR: Progress is reported toward the goal of realizing an array of primary hepatocytes for use in high-throughput liver toxicity studies through the development of a 64- element array of microfluidic wells capable of supporting micropatterned primary rat hepatocytes in coculture with 3T3-J2 fibroblasts.