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Nathan C. Gianneschi

Researcher at Northwestern University

Publications -  256
Citations -  10013

Nathan C. Gianneschi is an academic researcher from Northwestern University. The author has contributed to research in topics: Chemistry & Polymer. The author has an hindex of 47, co-authored 218 publications receiving 7446 citations. Previous affiliations of Nathan C. Gianneschi include University of California, Berkeley & University of California, San Diego.

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Artificial melanin nanoparticles and methods including porous melanin materials

TL;DR: In this paper, a plurality of artificial melanin nanoparticles are provided, wherein each melanin particle of the plurality of melanin oligomers comprises an oligomer and each oligomer comprises a covalently-bonded melanin base unit.
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A novel polymeric peptide delivery platform and association with targeted co-delivery of antigens and STING agonists with antitumor immune response.

TL;DR: This work validates the potential of PLPs to overcome major limitations in cancer vaccine development and develops rationally designed vaccines using a novel nanoplatform called the Protein-Like Polymer (PLP), with unique characteristics that allow for sustained/targeted delivery of tumor antigens in conjunction with STING agonists.
Posted Content

Structural Color Production in Melanin-based Disordered Colloidal Nanoparticle Assemblies in Spherical Confinement

TL;DR: Using a combined molecular dynamics and finite-difference time-domain computational approach, the authors investigates structural color generation in one-component melanin nanoparticle-based supra-assemblies (called supraballs) as well as binary mixtures of melanin and silica (nonabsorbing) nanoparticles-based suplaballs.
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Hierarchical Spidroin Micellar Nanoparticles as the Precursors of Spider Silks

TL;DR: In this paper, Lucas Parent et al. presented an analysis of the relationship between the magnetic resonance image (MRI) and the molecular magnetic resonance imaging (VMIA) at the University of Connecticut's Innovation Partnership Building.
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First-in-class heterobifunctional proteomimetic polymer capable of direct inhibition of Myc and target it for degradation

TL;DR: In this paper , the first helix (H1) of the bHLH-LZ region has been used to derive inhibitory peptides derived from the proto-oncogene Myc.