Repair of Endogenous DNA Damage

Rate of depurination of native deoxyribonucleic acid

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Quality Control by DNA Repair

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Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA

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Accumulation of premutagenic DNA lesions in mice defective in removal of oxidative base damage

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Mutagenic deamination of cytosine residues in DNA

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Second pathway for completion of human DNA base excision‐repair: reconstitution with purified proteins and requirement for DNase IV (FEN1)

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Reconstitution of DNA base excision‐repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein.

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DNA-bound structures and mutants reveal abasic DNA binding by APE1 DNA repair and coordination

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A superfamily of conserved domains in DNA damage‐ responsive cell cycle checkpoint proteins

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Comparison of Antioxidant Constituents of Agriophyllum squarrosum Seed with Conventional Crop Seeds

Xu, H. Y., Zheng, H., Zhang, H., Zhang, J., & Ma, C. (2018) · Journal of Food Science · doi:10.1111/1750-3841.14159 · Cited by 20

Introduction to the Molecular Biology of the Cell

Marín-García, J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404599-6.00001-9 · Cited by 20

Role of Yoga and Its Plausible Mechanism in the Mitigation of DNA Damage in Type-2 Diabetes: A Randomized Clinical Trial

Nair, R. G., Vasudev, M. M., & Mavathur, R. N. (2021) · Annals of Behavioral Medicine · doi:10.1093/abm/kaab043 · Cited by 19

Tcf-1 promotes genomic instability and T cell transformation in response to aberrant β-catenin activation

Arnovitz, S., Mathur, P., Tracy, M., Mohsin, A., Mondal, S., Quandt, J., Hernandez, K. M., Khazaie, K., Dose, M., Emmanuel, A. O., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2201493119 · Cited by 19

Base excision repair and double strand break repair cooperate to modulate the formation of unrepaired double strand breaks in mouse brain

Polyzos, A. A., Cheong, A. W. Y., Yoo, J. H., Blagec, L., Toprani, S. M., Nagel, Z. D., & McMurray, C. T. (2024) · Nature Communications · doi:10.1038/s41467-024-51906-5 · Cited by 19

Biomolecular Modifications Linked to Oxidative Stress in Amyotrophic Lateral Sclerosis: Determining Promising Biomarkers Related to Oxidative Stress

Hosaka, T., Tsuji, H., & Tamaoka, A. (2021) · Processes · doi:10.3390/pr9091667 · Cited by 20

Reactive oxygen species in colorectal cancer adjuvant therapies

Zhang, Y., Hao, M., Yang, X., Zhang, S., Han, J., Wang, Z., & Chen, H. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166922 · Cited by 21

Increased DNA damage in full-grown oocytes is correlated with diminished autophagy activation

Sun, F., Ali, N. N., Londoño-Vásquez, D., Simintiras, C. A., Qiao, H., Ortega, M. S., Ağca, Y., Takahashi, M., Rivera, R. M., Kelleher, A. M., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53559-w · Cited by 19

Protective Effect of Selenium-Enriched Ricegrass Juice against Cadmium-Induced Toxicity and DNA Damage in HEK293 Kidney Cells

Chomchan, R., Siripongvutikorn, S., Maliyam, P., Saibandith, B., & Puttarak, P. (2018) · Foods · doi:10.3390/foods7060081 · Cited by 18

Protection from Ultraviolet Damage and Photocarcinogenesis by Vitamin D Compounds

Silva, W. G. M. D., Abboud, M., Yang, C., Dixon, K. M., Rybchyn, M. S., & Mason, R. S. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-46227-7_12 · Cited by 18

‘Knock down’ of DNA polymerase β by RNA interference: recapitulation of null phenotype

Polosina, Y. Y., Rosenquist, T. A., Grollman, A. P., & Miller, H. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.05.011 · Cited by 18

USP1 in regulation of DNA repair pathways

Aboukheili, A. M. M., & Walden, H. (2025) · DNA repair · doi:10.1016/j.dnarep.2025.103807 · Cited by 17

Regulation of the Cell-Intrinsic DNA Damage Response by the Innate Immune Machinery

Hayman, T. J., & Glazer, P. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312761 · Cited by 19

BCL10 regulates RNF8/RNF168-mediated ubiquitination in the DNA damage response

Zhao, H., Zhu, M., Dou, G., Zhao, H., Zhu, B., Li, J., Liao, J., & Xu, X. (2014) · Cell Cycle · doi:10.4161/cc.28707 · Cited by 17

Destabilization of the PCNA trimer mediated by its interaction with the NEIL1 DNA glycosylase

Prakash, A., Moharana, K., Wallace, S. S., & Doublié, S. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1282 · Cited by 17

The fate of cells undergoing spontaneous DNA damage during development

Miermont, A., Antolović, V., Lenn, T., Nichols, J. M. E., Millward, L. J., & Chubb, J. R. (2019) · Development · doi:10.1242/dev.174268 · Cited by 17

Mathematical Modeling of p53 Pathways

Kim, E., Kim, J.-Y., & Lee, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20205179 · Cited by 17

Rapid Quantification of Oxidation and UV Induced DNA Damage by Repair Assisted Damage Detection-(Rapid RADD)

Gilat, N., Torchinsky, D., Margalit, S., Michaeli, Y., Avraham, S., Sharim, H., Elkoshi, N., Levy, C., Zirkin, S., & Ebenstein, Y. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c01393 · Cited by 16

Bovine Leukemia Virus Infection Affects Host Gene Expression Associated with DNA Mismatch Repair

Bai, L., Hirose, T., Assi, W., Wada, S., Takeshima, S., & Aida, Y. (2020) · Pathogens · doi:10.3390/pathogens9110909 · Cited by 17

The Potential Role of 8-Oxoguanine DNA Glycosylase-Driven DNA Base Excision Repair in Exercise-Induced Asthma

Belanger, K. K., Ameredes, B. T., Boldogh, I. R., & Aguilera-Aguirre, L. (2016) · Mediators of Inflammation · doi:10.1155/2016/3762561 · Cited by 19

The effects of metal ion contaminants on the double stranded DNA helix and diseases

Theophanides, T., & Anastassopoulou, J. (2017) · Journal of Environmental Science and Health Part A · doi:10.1080/10934529.2017.1328950 · Cited by 16

From single-molecule to genome-wide mapping of DNA lesions: repair-assisted damage detection sequencing

Gilat, N., Fridman, D., Sharim, H., Margalit, S., Gassman, N. R., Michaeli, Y., & Ebenstein, Y. (2021) · Biophysical Reports · doi:10.1016/j.bpr.2021.100017 · Cited by 17

The 8-oxoguanine DNA glycosylase 1 (ogg1) decreases the vulnerability of the developing brain to DNA damage

Gu, A., Ji, G., Yan, L., & Zhou, Y. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.08.018 · Cited by 16

Buried territories: heterochromatic response to DNA double-strand breaks

Feng, Y.-L., Xiang, J.-F., Kong, N., Cai, X., & Xie, A. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw033 · Cited by 16

Nucleostemin reveals a dichotomous nature of genome maintenance in mammary tumor progression

Lin, T., Lin, T.-C., McGrail, D. J., Bhupal, P. K., Ku, Y.-H., Zhang, W., Meng, L., Lin, S., Peng, G., & Tsai, R. Y. L. (2019) · Oncogene · doi:10.1038/s41388-019-0710-0 · Cited by 18

8-Oxoguanine DNA glycosylase1–driven DNA repair—A paradoxical role in lung aging

Germán, P., Saenz, D. N., Szaniszlo, P., Aguilera-Aguirre, L., Pan, L., Hegde, M. L., Bácsi, A., Hajas, G., Radak, Z. O., Ba, X., et al. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.06.009 · Cited by 16

Dual enzyme-assisted one-step isothermal real-time amplification assay for ultrasensitive detection of polynucleotide kinase activity

Li, X., Du, Y., Pan, Y.-N., Su, L.-L., Shi, S., Wang, S.-Y., Tang, A., Kim, K., & Kong, D. (2018) · Chemical Communications · doi:10.1039/c8cc08616h · Cited by 15

Cancer and the breakdown of multicellularity: What Dictyostelium discoideum, a social amoeba, can teach us

Mathavarajah, S., VanIderstine, C., Dellaire, G., & Huber, R. J. (2021) · BioEssays · doi:10.1002/bies.202000156 · Cited by 19

hMOB2 deficiency impairs homologous recombination-mediated DNA repair and sensitises cancer cells to PARP inhibitors

Gündoğdu, R., Erdoğan, M. K., Ditsiou, A., Spanswick, V. J., García-Gómez, J. J., Hartley, J. A., Esashi, F., Hergovich, A., & Gómez, V. (2021) · Cellular Signalling · doi:10.1016/j.cellsig.2021.110106 · Cited by 16

Base excision repair accessory factors in senescence avoidance and resistance to treatments

Vickridge, E., Faraco, C. C. F., & Nepveu, A. (2022) · Cancer Drug Resistance · doi:10.20517/cdr.2022.36 · Cited by 15

Cosmic Ionizing Radiation: A DNA Damaging Agent That May Underly Excess Cancer in Flight Crews

Toprani, S. M., Scheibler, C., Mordukhovich, I., McNeely, E., & Nagel, Z. D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147670 · Cited by 19

Electrochemical immunosensor for the predictive cancer biomarker SLFN11 using reduced graphene oxide/MIL-101(Cr)-NH2 composite

Kanagavalli, P., Elkaffas, R. A., Mohideen, M. I. H., & Eissa, S. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.138174 · Cited by 15

Ubiquitylation of DNA polymerase λ

Markkanen, E., van Loon, B., Ferrari, E. S., & Hübscher, U. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.03.069 · Cited by 15

Watching a double strand break repair polymerase insert a pro-mutagenic oxidized nucleotide

Jamsen, J. A., Sassa, A., Shock, D. D., Beard, W. A., & Wilson, S. H. (2021) · Nature Communications · doi:10.1038/s41467-021-21354-6 · Cited by 15

Biochemical identification of a hydroperoxide derivative of the free 8-oxo-7,8-dihydroguanine base

Hajas, G., Bácsi, A., Aguilera-Aguirre, L., Germán, P., Radak, Z. O., Sur, S., Hazra, T. K., & Boldogh, I. R. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.11.015 · Cited by 15

The response to the DNA damaging agent methyl methanesulfonate in a fungal plant pathogen

Milo, S., Pareek, M., Delulio, G., Almog, Y., Anand, G., Ma, L., & Covo, S. (2019) · Fungal Biology · doi:10.1016/j.funbio.2019.03.007 · Cited by 15

Redox Regulation in the Base Excision Repair Pathway: Old and New Players as Cancer Therapeutic Targets

Rajapakse, A., Suraweera, A., Boucher, D., Naqi, A., O'Byrne, K. J., Richard, D. J., & Croft, L. V. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867326666190430092732 · Cited by 15

Diverse functions of DNA glycosylases processing oxidative base lesions in brain

Scheffler, K., Bjørås, K. Ø., & Bjørås, M. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102665 · Cited by 13

Impact of Oxidative DNA Damage and the Role of DNA Glycosylases in Neurological Dysfunction

de Sousa, M. M. L., Ye, J., Luna, L., Hildrestrand, G. A., Bjørås, K. Ø., Scheffler, K., & Bjørås, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312924 · Cited by 17

Induction of homologous recombination by site-specific replication stress

Triplett, M. K., Johnson, M. J., & Symington, L. S. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103753 · Cited by 14

The intrinsic ATPase activity of Mycobacterium tuberculosis UvrC is crucial for its damage‐specific DNA incision function

Thakur, M., Agarwal, A., & Muniyappa, K. (2020) · FEBS Journal · doi:10.1111/febs.15465 · Cited by 14

Exploring the SSBreakome: genome‐wide mapping of DNA single‐strand breaks by next‐generation sequencing

Zilio, N., & Ulrich, H. D. (2020) · FEBS Journal · doi:10.1111/febs.15568 · Cited by 17

Bromodomain proteins: protectors against endogenous DNA damage and facilitators of genome integrity

Lee, S. Y., Kim, J. J., & Miller, K. M. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00673-0 · Cited by 15

Individual Genetic Heterogeneity

Vihinen, M. (2022) · Genes · doi:10.3390/genes13091626 · Cited by 17

The mismatch repair pathway functions normally at a non-AID target in germinal center B cells

Green, B., Belcheva, A., Nepal, R. M., Boulianne, B., & Martín, A. (2011) · Blood · doi:10.1182/blood-2011-03-345991 · Cited by 15

The Slx4-Dpb11 scaffold complex: coordinating the response to replication fork stalling in S-phase and the subsequent mitosis

Princz, L. N., Gritenaite, D., & Pfander, B. (2014) · Cell Cycle · doi:10.4161/15384101.2014.989126 · Cited by 16

Altération de la réparation de l’ADN et cancer

Rancoule, C., Vallard, A., Guy, J., Espenel, S., Sauvaigo, S., Rodriguez‐Lafrasse, C., & Magné, N. (2017) · Bulletin du Cancer · doi:10.1016/j.bulcan.2017.09.006 · Cited by 13

Inhibition of 8-oxoguanine DNA glycosylase (OGG1) expression suppresses polycystic ovarian syndrome via the NF-κB signaling pathway

Xia, J., Wu, S., Wu, G., & Yang, J. (2022) · Reproductive Biology · doi:10.1016/j.repbio.2022.100679 · Cited by 13

Background radiation and cancer risks: A major intellectual confrontation within the domain of radiation genetics with multiple converging biological disciplines

Calabrese, E. J., & Selby, P. B. (2023) · Journal of Occupational and Environmental Hygiene · doi:10.1080/15459624.2023.2252032 · Cited by 13

Origin of Genome Instability and Determinants of Mutational Landscape in Cancer Cells

Mehrotra, S., & Mittra, I. (2020) · Genes · doi:10.3390/genes11091101 · Cited by 14

Effect of Sepatronium Bromide (YM-155) on DNA Double-Strand Breaks Repair in Cancer Cells

Majera, D., & Mistrík, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249431 · Cited by 13

DNA Damage-Induced RNAPII Degradation and Its Consequences in Gene Expression

Muñoz, J. C., Beckerman, I., Choudhary, R., Bouvier, L. A., & Muñoz, M. J. (2022) · Genes · doi:10.3390/genes13111951 · Cited by 13

Reduced nerve growth factor levels in stress-related brain regions of folate-deficient mice

Eckart, S., Hörtnagl, H., Kronenberg, G., Gertz, K. R., Hörster, H., Endres, M., & Hellweg, R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.04.014 · Cited by 13

Modeling the Study of DNA Damage Responses in Mice

Specks, J., Nieto-Soler, M., Lopez-Contreras, A. J., & Fernández-Capetillo, Ó. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2297-0_21 · Cited by 13

RAD18 polymorphisms are associated with platinum-based chemotherapy toxicity in Chinese patients with non-small cell lung cancer

Chu, T., Li, R., Shao, M.-H., Ye, J.-Y., & Han, B. (2016) · Acta Pharmacologica Sinica · doi:10.1038/aps.2016.100 · Cited by 12

The Role of Oncogenic Tyrosine Kinase NPM-ALK in Genomic Instability

Lobello, C., Bikos, V., Janíková, A., & Pospı́šilová, Š. (2018) · Cancers · doi:10.3390/cancers10030064 · Cited by 13

Deciphering the dynamic code: DNA recognition by transcription factors in the ever-changing genome

Yao, Y. M., Miodownik, I., O’Hagan, M., Jbara, M., & Afek, A. (2024) · Transcription · doi:10.1080/21541264.2024.2379161 · Cited by 12

Interaction dynamics and site-specific electronic recognition of DNA-nicks with 2D solid-state nanopores

Athreya, N. B. M., Milenković, O., & Leburton, J. (2020) · npj 2D Materials and Applications · doi:10.1038/s41699-020-00166-0 · Cited by 12

Functional Roles of Homologous Recombination and Non-Homologous End Joining in DNA Damage Response and Microevolution in Cryptococcus neoformans

Jung, K., Jung, J., & Park, H. Y. (2021) · Journal of Fungi · doi:10.3390/jof7070566 · Cited by 14

Mild phenotype of knockouts of the major apurinic/apyrimidinic endonuclease APEX1 in a non-cancer human cell line

Kim, D. V., Kulishova, L. M., Torgasheva, N. A., Melentyev, V. S., Dianov, G. L., Medvedev, S. P., Zakian, S. M., & Zharkov, D. O. (2021) · PLoS ONE · doi:10.1371/journal.pone.0257473 · Cited by 11

Functional importance and divergence of plant apurinic/apyrimidinic endonucleases in somatic and meiotic DNA repair

Li, J., Wang, C., Liang, W., Zhang, J., Jiang, C., Liu, Y., Ren, Z., Ci, D., Chang, J., Han, S., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad056 · Cited by 12

A Structural Perspective on the Regulation of Human Single-Stranded DNA Binding Protein 1 (hSSB1, OBFC2B) Function in DNA Repair

Lawson, T., El‐Kamand, S., Kariawasam, R., Richard, D. J., Cubeddu, L., & Gamsjaeger, R. (2019) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2019.03.014 · Cited by 12

DNA repair, insulin signaling and sirtuins: at the crossroads between cancer and aging

Mostoslavsky, R. (2008) · Frontiers in bioscience · doi:10.2741/3203 · Cited by 11

Clinical and Mechanistic Implications of R-Loops in Human Leukemias

Lee, S. Y., Miller, K. M., & Kim, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065966 · Cited by 11

Discovery of a 53BP1 Small Molecule Antagonist Using a Focused DNA-Encoded Library Screen

Shell, D. J., Foley, C. A., Wang, Q., Smith, C. M., Guduru, S. K. R., Zeng, H., Dong, A., Norris-Drouin, J. L., Axtman, M., Hardy, P. B., et al. (2023) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.3c01192 · Cited by 12

Endogenous base damage as a driver of genomic instability in homologous recombination-deficient cancers

Aubuchon, L. N., & Verma, P. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103736 · Cited by 11

Icaritin inhibits PLK1 to activate DNA damage response in NK/T cell lymphoma and increases sensitivity to GELOX regime

Zhang, C.-J., Xu, H., Sui, X., Chen, L., Chen, B., Lv, H., Wang, S., & Wang, X. (2022) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2022.04.012 · Cited by 11

SN-38 Sensitizes BRCA-Proficient Ovarian Cancers to PARP Inhibitors through Inhibiting Homologous Recombination Repair

Lin, S., Tian, J., He, Q., Yang, M., Chen, Z., Belogurov, A. A., Li, X., Zhang, F., Liu, Y., & Chen, G. (2022) · Disease Markers · doi:10.1155/2022/7243146 · Cited by 11

Exogenous Plant-Based Nutraceutical Supplementation and Peripheral Cell Mononuclear DNA Damage Following High Intensity Exercise

Williamson, J., Hughes, C., & Davison, G. W. (2018) · Antioxidants · doi:10.3390/antiox7050070 · Cited by 11

The role of DNA damage as a therapeutic target in autosomal dominant polycystic kidney disease

Zhang, J. Q. J., Saravanabavan, S., Munt, A., Wong, A. T. Y., Harris, D. C. H., Harris, P. C., Wang, Y., & Rangan, G. K. (2019) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2019.6 · Cited by 12

Target-Based Radiosensitization Strategies: Concepts and Companion Animal Model Outlook

Berry, M. R., & Fan, T. M. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.768692 · Cited by 11

Hypothesis: RNA and DNA Viral Sequence Integration into the Mammalian Host Genome Supports Long-Term B Cell and T Cell Adaptive Immunity

Hurwitz, J. L., Jones, B. G., Charpentier, E., & Woodland, D. L. (2017) · Viral Immunology · doi:10.1089/vim.2017.0099 · Cited by 11

Inhibitors against DNA Polymerase I Family of Enzymes: Novel Targets and Opportunities

Kannan, S. R., Gillespie, S. W., Picking, W. L., Picking, W. D., Lorson, C. L., & Singh, K. (2024) · Biology · doi:10.3390/biology13040204 · Cited by 10

Mapping functional elements of the DNA damage response through base editor screens

Pan, Q., Zhang, Z., Xiong, Y., Bao, Y., Chen, T., Xu, P., Liu, Z., Ma, H., Yu, Y., Zhou, Z. L., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.115047 · Cited by 10

A predictive chromatin architecture nexus regulates transcription and DNA damage repair

Bhat, A., Bhan, S., Kabiraj, A., PANDITA, R. K., Ramos, K. S., Nandi, S., Sopori, S., Sarkar, P. S., Dhar, A., Pandita, S., et al. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.108300 · Cited by 12

OxiDIP-Seq for Genome-wide Mapping of Damaged DNA Containing 8-Oxo-2'-Deoxyguanosine

Gorini, F., Scala, G., Ambrosio, S., Majello, B., & Amente, S. (2022) · BIO-PROTOCOL · doi:10.21769/bioprotoc.4540 · Cited by 12

Aberrant HMGA2 Expression Sustains Genome Instability That Promotes Metastasis and Therapeutic Resistance in Colorectal Cancer

Gudiño, R. C., McManus, K. J., & Hombach‐Klonisch, S. (2023) · Cancers · doi:10.3390/cancers15061735 · Cited by 10

P53 and taurine upregulated gene 1 promotes the repair of the DeoxyriboNucleic Acid damage induced by bupivacaine in murine primary sensory neurons

Lai, L., Wang, Y., Peng, S., Guo, W., Li, F., & Xu, S. (2022) · Bioengineered · doi:10.1080/21655979.2022.2048985 · Cited by 11

PPP4C facilitates homologous recombination DNA repair by dephosphorylating PLK1 during early embryo development

Dong, M., Ouyang, Y., Gao, S.-C., Ma, X., Hou, Y., Schatten, H., Wang, Z., & Sun, Q. (2022) · Development · doi:10.1242/dev.200351 · Cited by 13

8-Oxo-2′-deoxyguanosine Replication in Mutational Hot Spot Sequences of the p53 Gene in Human Cells Is Less Mutagenic than That of the Corresponding Formamidopyrimidine

Stanio, S., Bacurio, J. H. T., Yang, H., Greenberg, M. M., & Basu, A. K. (2023) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.3c00069 · Cited by 10

In Vitro Lesion Bypass Studies of O4-Alkylthymidines with Human DNA Polymerase η

Williams, N. L., Wang, P., Wu, J., & Wang, Y. (2016) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.5b00509 · Cited by 10

Cell-Cycle Control and DNA-Damage Signaling in Mammals

Gómez, V., & Hergovich, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00014-8 · Cited by 12

Upregulation of mNEIL3 inOgg1-null cells is a potential backup mechanism for 8-oxoG repair

Higgs, E. B., Godschalk, R., Langie, S. A. S., van Schooten, F., & Hodges, N. J. (2021) · Mutagenesis · doi:10.1093/mutage/geab038 · Cited by 9

Regenerated Cellulose and Composites for Biomedical Applications

Zamel, D., Khan, A. U., Khan, A. N., Waris, A., Ilyas, M., Ali, A., & Baset, A. (2023) · Engineering materials · doi:10.1007/978-981-99-1655-9_10 · Cited by 9

HR repair pathway plays a crucial role in maintaining neural stem cell fate under irradiation stress

Xu, X. L., An, H., Wu, C., Sang, R., Wu, L., Lou, Y., Yang, X., & Xi, Y. (2023) · Life Science Alliance · doi:10.26508/lsa.202201802 · Cited by 9

Implications of Translesion DNA Synthesis Polymerases on Genomic Stability and Human Health

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Advances in the role of long non‑coding RNAs and RNA‑binding proteins in regulating DNA damage repair in cancer cells

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