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John Paul Pezacki

Researcher at University of Ottawa

Publications -  165
Citations -  6673

John Paul Pezacki is an academic researcher from University of Ottawa. The author has contributed to research in topics: RNA & RNA silencing. The author has an hindex of 40, co-authored 159 publications receiving 6093 citations. Previous affiliations of John Paul Pezacki include McMaster University & National Institute for Nanotechnology.

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Genomic analysis of the host response to hepatitis C virus infection.

TL;DR: Gene expression analysis of liver biopsies in acutely infected chimpanzees reveals genome-wide transcriptional changes that reflect the establishment, spread, and control of infection, and they reveal potentially unique antiviral programs associated with clearance of HCV infection.
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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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Gene expression during the priming phase of liver regeneration after partial hepatectomy in mice

TL;DR: Using high-density oligonucleotide arrays, the gene-expression program in the livers of mice after partial hepatectomy is examined to provide a detailed and comprehensive map of the initial priming stage of liver regeneration.
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Three-Mode Electrochemical Sensing of Ultralow MicroRNA Levels

TL;DR: A three-mode electrochemical sensor for detection and quantitation of ultralow levels of miRNAs in a wide dynamic range of measured concentrations and the H- and P-SENS were successfully employed for direct detection and profiling of three endogenous mi RNAs in human serum.