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Release from quiescence stimulates the expression of human NEIL3 under the control of the Ras dependent ERK-MAP kinase pathway
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RPA physically interacts with the human DNA glycosylase NEIL1 to regulate excision of oxidative DNA base damage in primer-template structures
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Methylated DNA Causes a Physical Block to Replication Forks Independently of Damage Signalling, O6-Methylguanine or DNA Single-Strand Breaks and Results in DNA Damage
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Phosphorylated Nucleolin Interacts with Translationally Controlled Tumor Protein during Mitosis and with Oct4 during Interphase in ES Cells
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The mouse ortholog of NEIL3 is a functional DNA glycosylase in vitro and in vivo
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HARPing on about the DNA damage response during replication
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Transcriptional Synergy Mediated by SAF-1 and AP-1 CRITICAL ROLE OF N-TERMINAL POLYALANINE AND TWO ZINC FINGER DOMAINS OF SAF-1
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Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells
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Physical and functional interaction between human oxidized base-specific DNA glycosylase NEIL1 and flap endonuclease 1
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Long patch base excision repair in mammalian mitochondrial Genomes
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Interaction of the human DNA glycosylase NEIL1 with proliferating cell nuclear antigen - The potential for replication-associated repair of oxidized bases in mammaliangenomes
Hong Dou et al.
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The human Werner syndrome protein stimulates repair of oxidative DNA base damage by the DNA glycosylase NEIL1
Aditi Das et al.
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RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors
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The Werner and Bloom syndrome proteins catalyze regression of a model replication fork
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The metabolic syndrome resulting from a knockout of the NEIL1 DNA glycosylase
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The interaction site of Flap Endonuclease-1 with WRN helicase suggests a coordination of WRN and PCNA
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NEIL1 excises 3 ' end proximal oxidative DNA lesions resistant to cleavage by NTH1 and OGG1
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AP endonuclease-independent DNA base excision repair in human cells
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Mismatch repair in human nuclear extracts - Effects of internal DNA-hairpin structures between mismatches and excision-initiation nicks on mismatch correction and mismatch-provoked excision
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M Takao et al.
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HUNG2 is the major repair enzyme for removal of uracil from U:A matches, U:G mismatches, and U in single-stranded DNA, with hSMUG1 as a broad specificity backup
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I Boldogh et al.
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