Author

I. Boldogh

The University of Texas Medical Branch at Galveston

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

Biology Disciplines

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Biochemistry· 1 Microbiology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Assay:proteomics· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1

Frequent Co-Authors

A. Chakraborty· 1 shared A. Egesten· 1 shared A. H. Sarker· 1 shared A. Islam· 1 shared C. Dong· 1 shared C. Kalderen· 1 shared G. Sharma· 1 shared Gang Liu· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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1 shared paperBiochemistry

A. Chakraborty

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

OGG1-Binding to Oxidized Guanine Base in Viral DNA Overcomes Epstein-Barr Virus Latency

Wenjing Hao, Xiaoqi Wang, Jiabo Li, Gang Liu, Lang Pan, Xueqing Ba, I. Boldogh, Ziyuan Duan

This study shows that OGG1 binding to oxidized guanine in EBV DNA promotes reactivation by activating lytic genes, suggesting OGG1 as a therapeutic target.

bioRxiv · Jun 6, 2026 · PreprintMicrobiology

Site-specific acetylation of polynucleotide kinase 3-phosphatase (PNKP) regulates its distinct role in DNA repair pathways

A. Islam, A. Chakraborty, A. H. Sarker, U. K. Aryal, G. Sharma, I. Boldogh, T. Hazra

This study shows that acetylation of PNKP at K142 and K226 regulates its distinct roles in DNA repair pathways, with K142 involved in BER/SSBR and K226 in DSBR.

bioRxiv · Jun 21, 2023Biochemistry

OGG1 inhibitor TH5487 alleviates allergic airway inflammation in mice

L. Tanner, J. Bergwik, R. K. Bhongir, L. Pan, C. Dong, C. Kalderen, T. Helleday, I. Boldogh, M. Adner, A. Egesten

This study shows that TH5487, an OGG1 inhibitor, reduces allergic airway inflammation in mice by decreasing mucus production, immune cell recruitment, and proinflammatory cytokines.

bioRxiv · May 17, 2022 · PreprintPharmacology & Toxicology