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Ran Li

Researcher at Harvard University

Publications -  29
Citations -  2243

Ran Li is an academic researcher from Harvard University. The author has contributed to research in topics: In vivo & Tumor microenvironment. The author has an hindex of 16, co-authored 27 publications receiving 1639 citations. Previous affiliations of Ran Li include Massachusetts Institute of Technology & University of Michigan.

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TLR7/8-agonist-loaded nanoparticles promote the polarization of tumour-associated macrophages to enhance cancer immunotherapy.

TL;DR: The ability of rationally engineered drug–nanoparticle combinations to efficiently modulate tumour-associated macrophages for cancer immunotherapy is demonstrated and R848, an agonist of the toll-like receptors TLR7 and TLR8 identified in a morphometric-based screen, is a potent driver of the M1 phenotype in vitro.
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Microfluidic platforms for mechanobiology

TL;DR: In this paper, the authors discuss how microfluidics has transformed the study of mechanotransduction and discuss new biological insights that have been elucidated by using micro-fluidic experiments.
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Combination of fluid and solid mechanical stresses contribute to cell death and detachment in a microfluidic alveolar model.

TL;DR: This research describes new tools for studying the combined effects of fluid mechanical and solid mechanical stress on alveolar cells and highlights the role that surface tension forces may play in the development of clinical pathology, especially under conditions of surfactant dysfunction.
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Microfluidics: A New Tool for Modeling Cancer–Immune Interactions

TL;DR: Current assays are reviewed and the development of new microfluidic technologies for immunotherapy are discussed, showing their unique ability to capture the essential features of multiple cell type interactions in three-dimensions while allowing tight control of the microenvironment and real-time monitoring.
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Fabrication of two-layered channel system with embedded electrodes to measure resistance across epithelial and endothelial barriers.

TL;DR: A straightforward fabrication process for embedding Ag/AgCl electrodes within a two-layer poly(dimethylsiloxane) (PDMS) microfluidic chip where an upper and a lower channel are separated by a semiporous membrane allows for the reliable real-time measurement of transendothelial and transepithelial electrical resistance (TEER).