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Tingrui Pan

Researcher at University of California, Davis

Publications -  184
Citations -  5437

Tingrui Pan is an academic researcher from University of California, Davis. The author has contributed to research in topics: Pressure sensor & Microfluidics. The author has an hindex of 32, co-authored 175 publications receiving 4069 citations. Previous affiliations of Tingrui Pan include Chinese Academy of Sciences & University of Science and Technology of China.

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A Plug-and-Play, Drug-on-Pillar Platform for Combination Drug Screening Implemented by Microfluidic Adaptive Printing.

TL;DR: This study supports the feasibility of the drug-on-pillar platform for combination drug screening and has provided valuable insight into drug combination efficacy against breast cancer.
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Comparison of piezoresistive sensor to PicoPress® in in-vitro interface pressure measurement

TL;DR: Piezoresistive sensor may represent a viable alternative to PicoPress® in interface pressure measurement and was found to be more pronounced in the higher pressure range.
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Reconfigurable microfluidic dilution for high-throughput quantitative assays

TL;DR: The microfluidic dilution generator offers a high-throughput high-efficiency quantitative analytical alternative to conventional quantitative assay platforms, by simple manipulation of a minute amount of chemicals in a compact microfluidity device with minimal equipment requirement, which can serve as a facile tool for biochemical and biological analyses in regular laboratories, point-of-care settings and low-resource environments.
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Reversible deactivation of higher-order posterior parietal areas. I. Alterations of receptive field characteristics in early stages of neocortical processing.

TL;DR: There are profound top-down influences on sensory processing of early cortical areas in the somatosensory cortex with microfluidic thermal regulators developed by the authors' laboratories.
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Reconfigurable microfluidics combined with antibody microarrays for enhanced detection of T-cell secreted cytokines

TL;DR: It is demonstrated that ∼90% pure CD4 T-cells can be captured inside the device and that signals for three important T-cell secreted cytokines, tissue necrosis factor-alpha, interferon-gamma, and interleukin-2, may be enhanced by 2 to 3 folds through the use of reconfigurable microfluidics.