Preferential repair of oxidized base damage in the transcribed genes of mammalian cells - Wikidata - awgldk - TriplyDB

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

http://www.wikidata.org/entity/Q34675663

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DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers Gut Microbiota Imbalance and Base Excision Repair Dynamics in Colon Cancer The Response to Oxidative DNA Damage in Neurons: Mechanisms and Disease The current state of eukaryotic DNA base damage and repair New perspectives on oxidized genome damage and repair inhibition by pro-oxidant metals in neurological diseases The Fpg/Nei family of DNA glycosylases: substrates, structures, and search for damage Base excision repair and cancer Emerging roles of the nucleolus in regulating the DNA damage response: the noncanonical DNA repair enzyme APE1/Ref-1 as a paradigmatical example Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency Structural investigation of a viral ortholog of human NEIL2/3 DNA glycosylases Insights into the glycosylase search for damage from single-molecule fluorescence microscopy.New insights in the removal of the hydantoins, oxidation product of pyrimidines, via the base excision and nucleotide incision repair pathways.Base excision repair: a critical player in many games Premature aging and cancer in nucleotide excision repair-disorders.DNA damage triggers SAF-A and RNA biogenesis factors exclusion from chromatin coupled to R-loops removal.Prereplicative repair of oxidized bases in the human genome is mediated by NEIL1 DNA glycosylase together with replication proteins.Comet-FISH with strand-specific probes reveals transcription-coupled repair of 8-oxoGuanine in human cells.New paradigms in the repair of oxidative damage in human genome: mechanisms ensuring repair of mutagenic base lesions during replication and involvement of accessory proteins.The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis.The NEIL glycosylases remove oxidized guanine lesions from telomeric and promoter quadruplex DNA structures Targeted detection of in vivo endogenous DNA base damage reveals preferential base excision repair in the transcribed strand Role of human DNA glycosylase Nei-like 2 (NEIL2) and single strand break repair protein polynucleotide kinase 3'-phosphatase in maintenance of mitochondrial genome.Regulation of NEIL1 protein abundance by RAD9 is important for efficient base excision repair Oxidative genome damage and its repair: implications in aging and neurodegenerative diseases.The C-terminal Domain (CTD) of Human DNA Glycosylase NEIL1 Is Required for Forming BERosome Repair Complex with DNA Replication Proteins at the Replicating Genome: DOMINANT NEGATIVE FUNCTION OF THE CTD.Increased risk of lung cancer associated with a functionally impaired polymorphic variant of the human DNA glycosylase NEIL2.Neil2-null Mice Accumulate Oxidized DNA Bases in the Transcriptionally Active Sequences of the Genome and Are Susceptible to Innate Inflammation Regulation of active genome integrity and expression by Rad26p.Enhancement of NEIL1 protein-initiated oxidized DNA base excision repair by heterogeneous nuclear ribonucleoprotein U (hnRNP-U) via direct interaction.Preferential repair of DNA double-strand break at the active gene in vivo.Neil3, the final frontier for the DNA glycosylases that recognize oxidative damage.Down-regulation of 8-oxoguanine DNA glycosylase 1 expression in the airway epithelium ameliorates allergic lung inflammation Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity.Contribution of DNA unwrapping from histone octamers to the repair of oxidatively damaged DNA in nucleosomes.Cockayne Syndrome group B protein stimulates NEIL2 DNA glycosylase activity.Scaffold attachment factor A (SAF-A) and Ku temporally regulate repair of radiation-induced clustered genome lesions Mechanisms of base substitution mutagenesis in cancer genomes.DNA glycosylases search for and remove oxidized DNA bases.Oxidative genome damage and its repair in neurodegenerative diseases: function of transition metals as a double-edged sword.

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Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

http://www.wikidata.org/entity/Q34675663

description

2010 nî lūn-bûn

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2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@ast

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@en

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@nl

type

label

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@ast

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@en

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@nl

prefLabel

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@ast

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@en

Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

@nl

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JBC.M110.198796

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Journal of Biological Chemistry

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Preferential repair of oxidized base damage in the transcribed genes of mammalian cells

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Aditi Das

http://www.w3.org/2001/XMLSchema#string

Dibyendu Banerjee

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Istvan Boldogh

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Kishor K Bhakat

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Partha S Sarkar

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Sankar Mitra

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Santi M Mandal

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Soumita Das

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Tapas K Hazra

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P2860

Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome

Primary structure and binding activity of the hnRNP U protein: binding RNA through RGG box

Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo

High mobility group protein-1 (HMG-1) is a unique activator of p53

Characterization of the XRCC1-DNA ligase III complex in vitro and its absence from mutant hamster cells

Transcriptional synergy mediated by SAF-1 and AP-1: critical role of N-terminal polyalanine and two zinc finger domains of SAF-1

Human DNA glycosylases of the bacterial Fpg/MutM superfamily: an alternative pathway for the repair of 8-oxoguanine and other oxidation products in DNA

Identification and characterization of a human DNA glycosylase for repair of modified bases in oxidatively damaged DNA

Scaffold/matrix attachment region elements interact with a p300-scaffold attachment factor A complex and are bound by acetylated nucleosomes.

hnRNP U inhibits carboxy-terminal domain phosphorylation by TFIIH and represses RNA polymerase II elongation

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6006-6016

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scholarly article

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10.1074/JBC.M110.198796

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8

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286

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Muralidhar L. Hegde

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2010-12-17T00:00:00Z

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21169365

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3057786

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