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Michael H. Stewart

Researcher at United States Naval Research Laboratory

Publications -  89
Citations -  6906

Michael H. Stewart is an academic researcher from United States Naval Research Laboratory. The author has contributed to research in topics: Quantum dot & Förster resonance energy transfer. The author has an hindex of 36, co-authored 86 publications receiving 5975 citations. Previous affiliations of Michael H. Stewart include United States Department of the Navy & Los Alamos National Laboratory.

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Quantum dot display enhances activity of a phosphotriesterase trimer

TL;DR: Phosphotriesterase was engineered into a spontaneously forming trimer by appending it to a synthetic collagen-like triple-helix motif that increased the enzyme's catalytic rate and efficiency.
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The Role of Negative Charge in the Delivery of Quantum Dots to Neurons.

TL;DR: It is confirmed both that preferential uptake in neurons, and the lack of uptake in glia, is strongly associated with having a region of greater negative charge on the QD coating, as well as the future potential of using QDs as vehicles for trafficking proteins into cells continues to show promise.
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Three-Dimensional Solution-Phase Förster Resonance Energy Transfer Analysis of Nanomolar Quantum Dot Bioconjugates with Subnanometer Resolution

TL;DR: A detailed FRET study on a large set of QD–biomolecule conjugates is presented, which allows for a homogeneous solution-phase size, shape, and bioconjugation analysis.
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Site-specific cellular delivery of quantum dots with chemoselectively-assembled modular peptides

TL;DR: Modular peptides displaying both quantum dot bioconjugation motifs and specific subcellular targeting domains were constructed using a chemoselective aniline-catalyzed hydrazone coupling chemistry to facilitate their specific delivery to either the plasma membrane, endosomes, the cytosol or the mitochondria of target cells.
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Synthesis, Structure, and Reactivity of Four-, Five-, and Six-Coordinate Ruthenium Carbyne Complexes

TL;DR: In this paper, the Grubbs catalysts Ru(CHR)(PCy3)2Cl2 were used to synthesize square-planar carbyne complexes of the form Ru(C-p-C6H4Me)2X (X = F, Cl, Br, I, O3SCF3).