David B. Heisler
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
27
Citations
428
Est. group size
~2
Recurring co-author estimate
Active years
50
Publishing since 1977
David B. Heisler's research examines how cells defend themselves against viral and bacterial infections, including how cholesterol and lipid metabolism restrict microbial invasion, and how RNA structures like G-quadruplexes regulate gene expression. Recent work has also explored antiviral pathways that operate independently of interferons (a common immune-signaling system) and are targeted by poxvirus proteins. This work spans molecular virology, structural RNA biology, and cell biology using both experimental and bioinformatic approaches.
Publication output has grown over the past decade, rising from sporadic single papers in the late 2010s to a more consistent 3-5 publications per year since 2023.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- BPS2026 – Elucidating the role of the hnRNP K mRNA 3'-UTR G-quadruplex structure in mediating its interactions with miR-1249-3p
Biophysical Journal · 2026
- G-Quadruplex and i-Motif Structures in the <i>SHMT1</i> 5′UTR Modulate Gene Expression
ACS Omega · 2026
- BPS2025 - Anti-viral activities of host microRNA against the SARS-CoV-2 genome 3′ untranslated region
Biophysical Journal · 2025
- G-Quadruplex and i-Motif Structures in the <i>SHMT1</i> 5’UTR Modulate Gene Expression
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- [3 + 2] Cycloadditions of Tertiary Amine <i>N</i> -Oxides and Azoarenes as a Route to Substituted 1,2,4-Triazolidines
ACS Organic & Inorganic Au · 2025
- Exploiting bacterial effector proteins to uncover evolutionarily conserved antiviral host machinery
PLoS Pathogens · 2024
- FEAR antiviral response pathway is independent of interferons and countered by poxvirus proteins
Nature Microbiology · 2024
- Exploiting Bacterial Effector Proteins to Uncover Evolutionarily Conserved Antiviral Host Machinery
bioRxiv (Cold Spring Harbor Laboratory) · 2024
- A concerted mechanism involving ACAT and SREBPs by which oxysterols deplete accessible cholesterol to restrict microbial infection
eLife · 2023
- A FACT-ETS-1 Antiviral Response Pathway Restricts Viral Replication and is Countered by Poxvirus A51R Proteins
bioRxiv (Cold Spring Harbor Laboratory) · 2023
- Author response: A concerted mechanism involving ACAT and SREBPs by which oxysterols deplete accessible cholesterol to restrict microbial infection
2023
- A Concerted Mechanism Involving ACAT and SREBPs By which Oxysterols Deplete Accessible Cholesterol To Restrict Microbial Infection
bioRxiv (Cold Spring Harbor Laboratory) · 2022
- Pathogenic ubiquitination of GSDMB inhibits NK cell bactericidal functions
Cell · 2021
- ACD-crosslinked actin oligomers are potent toxins inhibiting formin-mediated actin polymerization
2016
- bioRxiv (Cold Spring Harbor Laboratory)×5
- Biomolecules×2
- Biophysical Journal×2
- Cell×1
- eLife×1
- Laura C. Brown
Biochemistry, Genetics and Molecular Biology · Indiana University
- Chelsea A. Simpson
Biochemistry, Genetics and Molecular Biology · Indiana University
- Julia C. van Kessel
Biochemistry, Genetics and Molecular Biology · Indiana University
- Dean A. Rowe‐Magnus
Biochemistry, Genetics and Molecular Biology · Indiana University
- Logan J. Geyman
Biochemistry, Genetics and Molecular Biology · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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