Associated Papers
A monofunctional-like mutant of DNA glycosylase NTHL1 changes the dynamics of DNA repair during acute oxidative stress.
Haslam J et al.
The Journal of Biological Chemistry, 2026
OGG1 and MUTYH DNA Glycosylases, the Dynamic Duo Against 8-Oxoguanine DNA Lesion: Structure, Regulation, and Novel Emerging Roles.
Gómez-Ramírez AP et al.
Biomolecules, 2026
DNA Damage and Repair in Thyroid Physiology and Disease.
Arczewska KD et al.
Endocrine Reviews, 2026
Impact of pesticide exposure on base excision repair gene polymorphisms in the Haryana population.
Gulia H et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals, 2025
Molecular Mechanisms of Preventable Causes of Oral Cancer and Precancer Through Polymorphism in DNA Base Excision Repair Genes in Patients with Tobacco Products Habits.
Sundaram E et al.
Journal of Maxillofacial and Oral Surgery, 2025
The OGG1 Ser326Cys polymorphism: molecular mechanisms of disease susceptibility and precision medicine applications.
Wang X et al.
Clinical Epigenetics, 2025
Oxidative DNA damage and DNA repair gene variants in differentiated thyroid cancer patients treated with radioactive iodine.
Avsar FN et al.
Endocrine, 2025
Molecular Duality of OGG1: From Genomic Guardian to Redox-Sensitive Modulator in Diseases.
Zhong R et al.
Antioxidants (basel, Switzerland), 2025
OGG1 augments the transcriptional activation of Foxp3 to promote iTreg differentiation for IBD alleviation.
Tian M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2025
Genetic Polymorphisms in Base Excision Repair (BER) and Nucleotide Excision Repair (NER) Pathways as Potential Biomarkers for Gynecological Cancers: A Comprehensive Literature Review.
Szatkowska M et al.
Cancers, 2025
OGG1S326C variant frequent in human populations facilitates inflammatory responses due to its extended interaction with DNA substrate.
Han J et al.
Proceedings of the National Academy of Sciences of the United States of America, 2025
Integrative Computational Analysis of Common EXO5 Haplotypes: Impact on Protein Dynamics, Genome Stability, and Cancer Progression.
Mazza F et al.
Journal of Chemical Information and Modeling, 2025
APEX1 Polymorphisms Affect Acute Myeloid Leukemia Risk, and Its Expression Is Involved in Cell Proliferation and Differentiation.
Gotoh N et al.
International Journal of Laboratory Hematology, 2025
Defective DNA repair: a putative nexus linking immunological diseases, neurodegenerative disorders, and cancer.
Andarawi S et al.
Mutagenesis, 2025
Genomic instability in ovarian cancer: Through the lens of single nucleotide polymorphisms.
Canchi Sistla H et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2025
Targeting the 8-oxodG Base Excision Repair Pathway for Cancer Therapy.
Piscone A et al.
Cells, 2025
A systematic review and functional in-silico analysis of genes and variants associated with amyotrophic lateral sclerosis.
Arreola-Aldape CA et al.
Frontiers in Neuroscience, 2025
The Human 8-oxoG DNA Glycosylase 1 (OGG1) Ser326Cys Polymorphism in Infertile Men.
González-Díaz CA et al.
Biomedicines, 2024
Investigating Tobacco's Impact on DNA Repair Genes and Risks in Oral Precancer and Cancer: A Comprehensive Research Study.
Mohammad S et al.
Journal of Maxillofacial and Oral Surgery, 2024
Polymorphic variants of the hOGG1, APEX1, XPD, SOD2, and CAT genes involved in DNA repair processes and antioxidant defense and their association with breast cancer risk.
Timofeeva АА et al.
Vavilovskii Zhurnal Genetiki I Selektsii, 2024
Influence of genetic polymorphisms of Hg metabolism and DNA repair on the frequencies of micronuclei, nucleoplasmic bridges, and nuclear buds in communities living in gold mining areas.
Espitia-Pérez L et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis, 2024
Polymorphisms of DNA Repair Genes in Thyroid Cancer.
Gielecińska A et al.
International Journal of Molecular Sciences, 2024
Genetic variations in DNA excision repair pathway contribute to the chemosensitivity and prognosis of acute myeloid leukemia.
Zhang A et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2024
Genetic Associations of Primary Angle-Closure Disease: A Systematic Review and Meta-Analysis.
Liang YJ et al.
Jama Ophthalmology, 2024
Are changes in olanzapine-induced liver enzyme levels associated with GSTT1, GSTM1, GSTP1, and OGG1 gene polymorphisms?
Elkama A et al.
Arhiv Za Higijenu Rada I Toksikologiju, 2024
Modulation of gene expression and influence of gene polymorphisms related to genotoxicity and redox status on occupational exposure to inhaled anesthetics.
Silva MAP et al.
International Journal of Hygiene and Environmental Health, 2024
Association between polymorphisms of the DNA repair genes RAD51 and OGG1 and risk of cardiovascular disease.
Alomair A et al.
Molecular Medicine Reports, 2024
Genetic and epigenetic alterations in DNA repair genes and treatment outcome of chemoradiotherapy in cervical cancer.
Kushwah AS et al.
Critical Reviews in Oncology/hematology, 2024
Decreased DNA repair capacity caused by exposure to metal mixtures is modulated by the PARP1 rs1136410 variant in newborns from a polluted metropolitan area.
Paz-Sabillón M et al.
Environmental Research, 2024
XRCC1 and hOGG1 polymorphisms and endometrial carcinoma: A meta-analysis.
He S et al.
Open Medicine (warsaw, Poland), 2024
Genetic polymorphisms and platinum-induced hematological toxicity: a systematic review.
Zheng Y et al.
Frontiers in Pharmacology, 2024
Quantitative assessment of the association between TNF-α gene polymorphisms and angina risk.
Xu S et al.
American Journal of Translational Research, 2024
The Incidence of the XRCC1 rs25487 and PON1 rs662 Polymorphisms in a Population from Central Brazil: Patterns in an Area with a High Level of Agricultural Activity.
Alves AA et al.
Biochemical Genetics, 2023
Understanding DNA Damage Response and DNA Repair in Multiple Myeloma.
Petrilla C et al.
Cancers, 2023
Single-Nucleotide Polymorphisms in Base-Excision Repair-Related Genes Involved in the Risk of an Occurrence of Non-Alcoholic Fatty Liver Disease.
Ziółkowska S et al.
International Journal of Molecular Sciences, 2023
Genetic variants in varicocele-related male infertility: a systematic review and future directions.
Mostafa T et al.
Human Fertility (cambridge, England), 2023
The ADORA2A TT Genotype Is Associated with Anti-Inflammatory Effects of Caffeine in Response to Resistance Exercise and Habitual Coffee Intake.
Rahimi MR et al.
Nutrients, 2023
Strong Cumulative Evidence of Associations of 6 Single Nucleotide Polymorphisms with Ovarian Cancer Risk: An Umbrella Review.
Huo YJ et al.
Journal of Clinical Medicine, 2023
Next-generation sequencing of prolidase gene identifies novel and common variants associated with low prolidase in coronary artery ectasia.
Pekkoc-Uyanik KC et al.
Molecular Biology Reports, 2023
Neural Tube Defects and Folate Deficiency: Is DNA Repair Defective?
Wang X et al.
International Journal of Molecular Sciences, 2023
The interplay between XPG-Asp1104His polymorphism and reproductive risk factors elevates risk of breast cancer in Tanzanian women: A multiple interaction analysis.
Adolf IC et al.
Cancer Medicine, 2023
Association of buccal micronucleus cytome assay (BMNCyt) biomarkers with inorganic element concentration and genetic polymorphisms in welders.
Quintana-Sosa M et al.
Environmental Toxicology and Pharmacology, 2023
Association of MTHFR C667T Polymorphism, Homocysteine, and B Vitamins with Senile Cataract.
Luo J et al.
Journal of Nutritional Science and Vitaminology, 2023
Complex Roles of NEIL1 and OGG1: Insights Gained from Murine Knockouts and Human Polymorphic Variants.
Lloyd RS
Dna, 2022
hOGG1 rs1052133 Polymorphism and Prostate Cancer Risk: A Chinese Case-Control Study and Meta-Analysis.
Xu H et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2022
Genetic susceptibility of bladder cancer in the Lebanese population.
Kourie HR et al.
Bmc Medical Genomics, 2022