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Colin Luo

Researcher at University of California, San Diego

Publications -  16
Citations -  592

Colin Luo is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Myocardial infarction & Medicine. The author has an hindex of 6, co-authored 12 publications receiving 433 citations.

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Enzyme-Responsive Nanoparticles for Targeted Accumulation and Prolonged Retention in Heart Tissue after Myocardial Infarction.

TL;DR: Enzyme-responsive peptide-polymer amphiphiles are assembled as spherical micellar nanoparticles, and undergo a morphological transition from spherical-shaped, discrete materials to network-like assemblies when acted upon by matrix metalloproteinases.
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Evidence for Mechanisms Underlying the Functional Benefits of a Myocardial Matrix Hydrogel for Post-MI Treatment

TL;DR: Results indicate that the myocardial matrix alters several key pathways after MI creating a pro-regenerative environment, further demonstrating its promise as a potential post-MI therapy.
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Coevolution within a transcriptional network by compensatory trans and cis mutations.

TL;DR: An example of "coevolution" between a DNA-binding transcription factor and its cis-regulatory site, reminiscent of the coevolution of protein binding partners, is demonstrated, that allows for conserved transcriptional regulation despite continued genetic change.
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Enzyme-responsive progelator cyclic peptides for minimally invasive delivery to the heart post-myocardial infarction

TL;DR: Cyclic peptides with low viscosity for catheter delivery are reported on, which form self-assembled peptide hydrogels following enzymatic cleavage and demonstrated delivery in vivo.
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A systems approach to delineate functions of paralogous transcription factors: Role of the Yap family in the DNA damage response

TL;DR: This analysis reveals that YAP regulatory specificity is achieved by at least three mechanisms: divergence of DNA-binding sequences into two subfamilies; condition-specific combinatorial regulation by multiple Yap factors; and interactions of Yap 1, 4, and 6 with chromatin remodeling proteins.