Author

A. Jozic

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioengineering· 3

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:drug response / drug discovery· 2 Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Organism:human· 1 Assay:imaging· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

G. Sahay· 3 shared J. Kim· 2 shared A. Kerr· 1 shared A. Mukherjee· 1 shared A. Roberts· 1 shared D. Nelson· 1 shared D. Sahel· 1 shared J. Walker· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersBioengineering

G. Sahay

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Synthesis of ionizable lipopolymers using split-Ugi reaction for pulmonary delivery of various size RNAs and gene editing

K. Y. Vlasova, A. Kerr, N. D. Pennock, A. Jozic, D. Sahel, M. Gautam, N. Murthy, A. Roberts, M. W. Ali, K. D. MacDonald, J. Walker, R. Luxenhofer, G. Sahay

The paper develops a method to deliver various RNA therapeutics, including mRNA and CRISPR-Cas9, to the lung using lipopolymer-lipid hybrid nanoparticles, showing improved efficacy and reduced toxicity.

bioRxiv · Jun 11, 2024Bioengineering

Illuminating endosomal escape of polymorphic lipid nanoparticles that boost mRNA delivery

M. Herrera, J. Kim, Y. Eygeris, A. Jozic, G. Sahay

This study uses a Gal8-GFP reporter system to compare endosomal escape efficiency of lipid nanoparticles with cholesterol versus phytosterols, finding that LNP-Sito shows significantly enhanced escape.

bioRxiv · Dec 2, 2020Bioengineering

Rapid generation of circulating and mucosal decoy ACE2 using mRNA nanotherapeutics for the potential treatment of SARS-CoV-2

J. Kim, A. Mukherjee, D. Nelson, A. Jozic, G. Sahay

This paper demonstrates the use of mRNA nanotherapeutics to generate soluble hACE2 for rapid neutralization of SARS-CoV-2 in both circulation and mucosal sites.

bioRxiv · Jul 24, 2020 · PreprintBioengineering