Associated Papers
Defective DNA repair: a putative nexus linking immunological diseases, neurodegenerative disorders, and cancer.
Andarawi S et al.
Mutagenesis, 2025
Pathogenic germline variants in Chinese pancreatic adenocarcinoma patients.
Yin X et al.
Nature Communications, 2025
Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer.
Adamson AW et al.
Journal of Ovarian Research, 2023
Whole genome sequencing identifies genetic variants associated with neurogenic inflammation in rosacea.
Deng Z et al.
Nature Communications, 2023
Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population.
Lin MR et al.
Journal of Personalized Medicine, 2022
Multi-omics analysis identifies osteosarcoma subtypes with distinct prognosis indicating stratified treatment.
Jiang Y et al.
Nature Communications, 2022
The correlation of combined OGG1, CYP1A1 and GSTP1 gene variants and risk of lung cancer of male Iraqi waterpipe tobacco smokers.
Kudhair BK et al.
Molecular Biology Reports, 2020
Chromatin and other obstacles to base excision repair: potential roles in carcinogenesis.
Caffrey PJ et al.
Mutagenesis, 2020
Catalytically Competent Conformation of the Active Site of Human 8-Oxoguanine-DNA Glycosylase.
Popov AV et al.
Biochemistry. Biokhimiia, 2020
Genetic polymorphisms and pancreatic cancer risk: A PRISMA-compliant systematic review and meta-analysis.
Dai P et al.
Medicine, 2019
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer.
Leong TL et al.
Oncogene, 2019
Thermostability and excision activity of polymorphic forms of hOGG1.
Mouzakis KD et al.
Bmc Research Notes, 2019
Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.
Pritchard AL et al.
Plos One, 2018
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
DeRycke MS et al.
Molecular Genetics & Genomic Medicine, 2017
Single nucleotide polymorphisms in DNA glycosylases: From function to disease.
D'Errico M et al.
Free Radical Biology & Medicine, 2017
Association between polymorphisms of APE1 and OGG1 and risk of colorectal cancer in Taiwan.
Lai CY et al.
World Journal of Gastroenterology, 2016
A systematic review and meta-analysis of the association between OGG1 Ser326Cys polymorphism and cancers.
Zhou PT et al.
Medical Oncology (northwood, London, England), 2015
Could 8-oxoguanine DNA glycosylase 1 Ser326Cys polymorphism be a biomarker of susceptibility in cancer?
Karahalil B et al.
Toxicology and Industrial Health, 2014
Association of c.461G>A genetic variant of OGG1 gene with pancreatic cancer susceptibility in Chinese.
Zhao ZM et al.
Genetics and Molecular Research : Gmr, 2014
Meta-analysis demonstrates lack of association of the hOGG1 Ser326Cys polymorphism with bladder cancer risk.
Zhong DY et al.
Genetics and Molecular Research : Gmr, 2012
Reprint of: gene susceptibility to oxidative damage: from single nucleotide polymorphisms to function.
Simonelli V et al.
Mutation Research, 2012
Clinical and molecular detection of inherited colorectal cancers in northeast Italy: a first prospective study of incidence of Lynch syndrome and MUTYH-related colorectal cancer in Italy.
Urso E et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2012
Gene susceptibility to oxidative damage: from single nucleotide polymorphisms to function.
Simonelli V et al.
Mutation Research, 2012
Lack of association between hOGG1 Ser326Cys polymorphism and the risk of bladder cancer: a meta-analysis.
Li D et al.
Urologia Internationalis, 2012
Variation in base excision repair capacity.
Wilson DM et al.
Mutation Research, 2011
8-Oxoguanine incision activity is impaired in lung tissues of NSCLC patients with the polymorphism of OGG1 and XRCC1 genes.
Janik J et al.
Mutation Research, 2011
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
Morak M et al.
European Journal of Cancer (oxford, England : 1990), 2011
OGG1 Ser326Cys polymorphism and susceptibility to esophageal cancer in low and high at-risk populations of northern India.
Upadhyay R et al.
Journal of Gastrointestinal Cancer, 2010
The C-terminal lysine of Ogg2 DNA glycosylases is a major molecular determinant for guanine/8-oxoguanine distinction.
Faucher F et al.
Journal of Molecular Biology, 2010
Substrate specificity and excision kinetics of natural polymorphic variants and phosphomimetic mutants of human 8-oxoguanine-DNA glycosylase.
Sidorenko VS et al.
The Febs Journal, 2009
The R46Q, R131Q and R154H polymorphs of human DNA glycosylase/beta-lyase hOgg1 severely distort the active site and DNA recognition site but do not cause unfolding.
Anderson PC et al.
Journal of the American Chemical Society, 2009
Crystal structures of two archaeal 8-oxoguanine DNA glycosylases provide structural insight into guanine/8-oxoguanine distinction.
Faucher F et al.
Structure (london, England : 1993), 2009
DNA repair dysfunction in gastrointestinal tract cancers.
Maehara Y et al.
Cancer Science, 2008
Association between genetic polymorphisms of the base excision repair gene MUTYH and increased colorectal cancer risk in a Japanese population.
Tao H et al.
Cancer Science, 2008
Contribution of common monoallelic MUTYH gene variants in German patients with familial colorectal cancer.
Grünhage F et al.
Cancer Biomarkers : Section a of Disease Markers, 2008
Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer.
Schafmayer C et al.
International Journal of Cancer, 2007
Polymorphisms in genes of nucleotide and base excision repair: risk and prognosis of colorectal cancer.
Moreno V et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2006
Modulation of oxidative mutagenesis and carcinogenesis by polymorphic forms of human DNA repair enzymes.
Nohmi T et al.
Mutation Research, 2005
Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients.
Kim IJ et al.
Human Genetics, 2004
Electronic microarray technique for detection of nine base substitutions including single-nucleotide polymorphisms in the human OGG1 gene.
Gong Z et al.
Clinical Chemistry, 2004
Effect of single mutations in the OGG1 gene found in human tumors on the substrate specificity of the Ogg1 protein.
Audebert M et al.
Nucleic Acids Research, 2000
Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA.
Bruner SD et al.
Nature, 2000
Oxidative DNA damage and human cancer: need for cohort studies.
Loft S et al.
Antioxidants & Redox Signaling, 0
Sporadic colorectal cancer and individual susceptibility: a review of the association studies investigating the role of DNA repair genetic polymorphisms.
Naccarati A et al.
Mutation Research, 0
Base excision repair modulation as a risk factor for human cancers.
Tudek B
Molecular Aspects of Medicine, 0