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Kris Barreto

Researcher at University of Saskatchewan

Publications -  24
Citations -  328

Kris Barreto is an academic researcher from University of Saskatchewan. The author has contributed to research in topics: Nimotuzumab & In vivo. The author has an hindex of 11, co-authored 24 publications receiving 221 citations.

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89 Zr-nimotuzumab for immunoPET imaging of epidermal growth factor receptor I

TL;DR: 89Zr-DFO-nimotuzumab had low organ absorbed dose and effective dose that makes it suitable for potential human use and there was no apparent normal tissue toxicity as shown by cell blood counts and blood biochemistry analyses at 168-fold and 25-fold excess of the projected human radioactive and mass dose of the agent.
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Synthetic Modular Antibody Construction by Using the SpyTag/SpyCatcher Protein-Ligase System.

TL;DR: A new way to construct recombinant antibody‐like “ devices” by using a bottom‐up approach to build them from well‐behaved discrete recombinant antibodies domains or “parts”, thereby creating devices with desired properties based on summed properties of parts and in configurations that cannot be obtained by using genetic engineering.
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Next-generation sequencing-guided identification and reconstruction of antibody CDR combinations from phage selection outputs.

TL;DR: An NGS-assisted antibody discovery platform by integrating phage-displayed, single-framework, synthetic Fab libraries is developed and a rapid and simple method for linking and sequencing all diversified CDRs in phage Fab pools is developed.
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Site-Specific Fluorescent Labeling of Antibodies and Diabodies Using SpyTag/SpyCatcher System for In Vivo Optical Imaging

TL;DR: Results highlight the ease and utility of using the modular SpyTag/SpyCatcher protein ligase system for site-specific fluorescent labeling of protein-based imaging probes and confirm the affinity and specificity of the IRDye800CW-labeled imaging probes.
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Evaluation of antibody fragment properties for near-infrared fluorescence imaging of HER3-positive cancer xenografts.

TL;DR: The utility of using antibody fragments to optimize clearance, tumor labeling, and biodistribution properties for developing anti-HER3 probes for image-guided surgery or PET imaging is highlighted.