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Bing Xu

Researcher at Brandeis University

Publications -  373
Citations -  29970

Bing Xu is an academic researcher from Brandeis University. The author has contributed to research in topics: Self-healing hydrogels & Cancer cell. The author has an hindex of 83, co-authored 357 publications receiving 26713 citations. Previous affiliations of Bing Xu include University of Pennsylvania & University of Hong Kong.

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Hyper‐Crosslinkers Lead to Temperature‐ and pH‐Responsive Polymeric Nanogels with Unusual Volume Change

TL;DR: As the first example of the use of functional hyper-crosslinkers to control the pH and thermal responses of nanogels, this work illustrates a new way to design soft materials with unusual behaviors.
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Chirality Controls Reaction-Diffusion of Nanoparticles for Inhibiting Cancer Cells.

TL;DR: As the first example of chirality controlling RD process of NPs for inhibiting cancer cells, this work illustrates a fundamentally new way for developing nanomedicine based on RD processes and nanoparticles.
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Synthesis of novel conjugates of a saccharide, amino acids, nucleobase and the evaluation of their cell compatibility.

TL;DR: This article reports the synthesis of a novel type of conjugate of three fundamental biological build blocks (i.e., saccharide, amino acids, and nucleobase) and their cell compatibility and their conjugates are mammalian cell compatible.
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Supramolecular hydrogel of kanamycin selectively sequesters 16S rRNA

TL;DR: The hydrogel of kanamycin indicates that the hydrogels of aminoglycosides preserve the specific interaction with their macromolecular targets (e.g., 16S rRNA), thus illustrating a simple approach to explore and identify possible biological targets of supramolecular nanofibers/hydrogels.
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Ectoenzyme switches the surface of magnetic nanoparticles for selective binding of cancer cells.

TL;DR: This work illustrates a fundamentally new concept to allow cells to actively engineer the surface of colloids materials, such as magnetic nanoparticles, for various applications as well as a general method to broadly target cancer cells without relying on specific ligand-receptor interactions.