Associated Papers
The Link Between Human Alkyladenine DNA Glycosylase and Cancer Development.
Kladova OA et al.
International Journal of Molecular Sciences, 2025
Aflatoxin B1-Induced Hepatic Mutagenesis in Mice Expressing Gene-Edited Neil1.
Minko IG et al.
Environmental and Molecular Mutagenesis, 2025
DNA repair and disease: insights from the human DNA glycosylase NEIL family.
Hwang Y et al.
Experimental & Molecular Medicine, 2025
Decoding the Role of NEIL1 Gene in DNA Repair and Lifespan: A Literature Review with Bioinformatics Analysis.
Mohajeri Khorasani A et al.
Advanced Biology, 2024
Functional analyses of single nucleotide polymorphic variants of the DNA glycosylase NEIL1 in sub-Saharan African populations.
Zuckerman JT et al.
Dna Repair, 2023
Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer.
Adamson AW et al.
Journal of Ovarian Research, 2023
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.
Alenezi WM et al.
Frontiers in Oncology, 2023
Complex Roles of NEIL1 and OGG1: Insights Gained from Murine Knockouts and Human Polymorphic Variants.
Lloyd RS
Dna, 2022
Mouse Embryonic Fibroblasts Isolated From Nthl1 D227Y Knockin Mice Exhibit Defective DNA Repair and Increased Genome Instability.
Marsden CG et al.
Dna Repair, 2022
Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents.
Olkinuora AP et al.
Frontiers in Oncology, 2022
Chromatin and other obstacles to base excision repair: potential roles in carcinogenesis.
Caffrey PJ et al.
Mutagenesis, 2020
The double-edged sword of cancer mutations: exploiting neoepitopes for the fight against cancer.
Alvarado-Cruz I et al.
Mutagenesis, 2020
Characterization of rare NEIL1 variants found in East Asian populations.
Minko IG et al.
Dna Repair, 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
The NEIL1 G83D germline DNA glycosylase variant induces genomic instability and cellular transformation.
Galick HA et al.
Oncotarget, 2017
Single nucleotide polymorphisms in DNA glycosylases: From function to disease.
D'Errico M et al.
Free Radical Biology & Medicine, 2017
NEIL1 p.Gln282Stop variant is predominantly localized in the cytoplasm and exhibits reduced activity in suppressing mutations.
Shinmura K et al.
Gene, 2015
Genome and cancer single nucleotide polymorphisms of the human NEIL1 DNA glycosylase: activity, structure, and the effect of editing.
Prakash A et al.
Dna Repair, 2014
NEIL1 responds and binds to psoralen-induced DNA interstrand crosslinks.
McNeill DR et al.
The Journal of Biological Chemistry, 2013
Oxidatively induced DNA damage: mechanisms, repair and disease.
Dizdaroglu M
Cancer Letters, 2012
Reprint of: gene susceptibility to oxidative damage: from single nucleotide polymorphisms to function.
Simonelli V et al.
Mutation Research, 2012
Gene susceptibility to oxidative damage: from single nucleotide polymorphisms to function.
Simonelli V et al.
Mutation Research, 2012
Variation in base excision repair capacity.
Wilson DM et al.
Mutation Research, 2011
Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma.
Forsbring M et al.
Carcinogenesis, 2009
Human polymorphic variants of the NEIL1 DNA glycosylase.
Roy LM et al.
The Journal of Biological Chemistry, 2007