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David J. Guckenberger

Researcher at University of Wisconsin-Madison

Publications -  40
Citations -  1112

David J. Guckenberger is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Tumor progression & Substrate (printing). The author has an hindex of 12, co-authored 40 publications receiving 868 citations. Previous affiliations of David J. Guckenberger include Wisconsin Alumni Research Foundation.

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Micromilling: a method for ultra-rapid prototyping of plastic microfluidic devices

TL;DR: This tutorial review offers protocols, tips, insight, and considerations for practitioners interested in using micromilling to create microfluidic devices to provide a potential user with information to guide them on whethermicromilling would fill a specific need within their overall fabrication strategy.
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Rapid Prototyping of Arrayed Microfluidic Systems in Polystyrene for Cell-Based Assays

TL;DR: A complete process is presented that describes the fabrication of polystyrene (PS) microfluidic devices with similar cost and time expenditures as PDMS-based devices with emphasis on creating methods that can compete with PDMS fabrication methods in terms of robustness, complexity, and time requirements.
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The VerIFAST: an integrated method for cell isolation and extracellular/intracellular staining

TL;DR: The VerIFAST is demonstrated, a device that builds upon the simplified workflow of the Immiscible Filtration Assisted by Surface Tension to integrate a method for cellular isolation with methods for extra- and intracellular staining.
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Fundamentals of rapid injection molding for microfluidic cell-based assays.

TL;DR: Advantages and limitations of rapid injection molding for microfluidic device fabrication through measurement of key features for cell culture applications including channel geometry, feature consistency, floor thickness, and surface polishing are characterized.
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High Specificity in Circulating Tumor Cell Identification Is Required for Accurate Evaluation of Programmed Death-Ligand 1

TL;DR: Interfering myeloid populations can be differentiated from true CTCs with additional staining criteria, thus improving the specificity of CTC identification and the accuracy of biomarker evaluation.