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Dana C. Danielson

Researcher at University of Ottawa

Publications -  8
Citations -  637

Dana C. Danielson is an academic researcher from University of Ottawa. The author has contributed to research in topics: RNA interference & RNA silencing. The author has an hindex of 6, co-authored 8 publications receiving 565 citations. Previous affiliations of Dana C. Danielson include National Research Council.

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Cellular consequences of copper complexes used to catalyze bioorthogonal click reactions.

TL;DR: It is shown that under conditions where other copper complexes kill human hepatoma cells, Cu(I)-L-histidine is an effective catalyst for CuAAC labeling of live cells following metabolic incorporation of an alkyne-labeled sugar into glycosylated proteins expressed on the cell surface.
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Chemical contrast for imaging living systems: molecular vibrations drive CARS microscopy

TL;DR: The nonlinear variant of Raman spectroscopy, coherent anti-Stokes Raman scattering (CARS) microscopy, combines powerful Raman signal enhancement with several other advantages such as label-free detection and has been used to image various cellular processes including host-pathogen interactions and lipid metabolism.
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Strain-promoted cycloadditions of cyclic nitrones with cyclooctynes for labeling human cancer cells

TL;DR: Strain-promoted cycloadditions of cyclic nitrones with cyclooctynes proceed with rate constants up to 59 times faster than the analogous reaction of azides, which can be applied for direct labeling of proteins and for live cell imaging of cancer cells.
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Studying the RNA silencing pathway with the p19 protein

TL;DR: The p19 protein is expressed by tombusviruses as a suppressor of RNA silencing and functions to sequester small RNA duplexes, thereby preventing induction of the pathway as mentioned in this paper.
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Enhanced specificity of the viral suppressor of RNA silencing protein p19 toward sequestering of human microRNA-122.

TL;DR: The results suggest that p19 can be engineered to enhance its affinity toward specific small RNA molecules, particularly noncanonical miRNAs that are distinguishable based on locations of base-pair mismatches.