Author

Julianna R. Cresti

University of MichiganORCID 0000-0003-2953-8720Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:bacteria (other)· 2 Research Focus:cell signaling & trafficking· 1 Approach:experimental assay· 1 Assay:fluorescence / live-cell microscopy· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

Lyle A. SimmonsiD· 2 shared Daniel J. FoustiD· 1 shared Frances Caroline LowderiD· 1 shared Jessica Chung· 1 shared Julie S. BiteeniD· 1 shared Lieke A. van GijtenbeekiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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2 shared papersBiophysics

Lyle A. SimmonsORCID

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2 papers

Recent·Most cited

BiophysicsBiophysical JournalPeer-reviewedJun 12, 2026

Single-molecule tracking of RNA-DNA hybrid removal enzymes important for lagging-strand replication

Daniel J. Foust, Frances Caroline Lowder, Jessica Chung…·Julie S. Biteen

This study uses single-molecule tracking to analyze the behavior of three proteins involved in removing RNA-DNA hybrids during lagging-strand replication in Bacillus subtilis, revealing their dynamic interactions with the replisome and nucleoid.

DOI 10.1016/j.bpj.2026.06.015

bacteria (other)fluorescence / live-cell microscopy

𝕏 PostBluesky

BiochemistryMolecular MicrobiologyPeer-reviewedJan 6, 2026

Bacillus subtilis RNase HII is inefficient at processing guanosine monophosphate and damaged ribonucleotides

Julianna R. Cresti, Lyle A. Simmons

This study compares the efficiency of RNase HII from Bacillus subtilis and Escherichia coli in processing various ribonucleotides, finding B. subtilis is inefficient at repairing damaged rNMPs.

2 citations

bacteria (other)experimental assay

𝕏 PostBluesky