The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA.
about
Functional consequences of mutations in the conserved SF2 motifs and post-translational phosphorylation of the CSB proteinCooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress.Cockayne syndrome protein B interacts with and is phosphorylated by c-Abl tyrosine kinaseAnalysis of Hemicentin-1, hOgg1, and E-selectin single nucleotide polymorphisms in age-related macular degenerationCockayne syndrome group B protein stimulates repair of formamidopyrimidines by NEIL1 DNA glycosylasePathways for repairing and tolerating the spectrum of oxidative DNA lesionsDNA repair diseases: What do they tell us about cancer and aging?Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediatesDifferent effects of CSA and CSB deficiency on sensitivity to oxidative DNA damageAn abundant evolutionarily conserved CSB-PiggyBac fusion protein expressed in Cockayne syndromeCreating context for the use of DNA adduct data in cancer risk assessment: II. Overview of methods of identification and quantitation of DNA damage.Proteins of nucleotide and base excision repair pathways interact in mitochondria to protect from loss of subcutaneous fat, a hallmark of agingCockayne syndrome group B cellular and biochemical functions.Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease.Elements That Regulate the DNA Damage Response of Proteins Defective in Cockayne SyndromeSynergic effect of polymorphisms in ERCC6 5' flanking region and complement factor H on age-related macular degeneration predispositionRole of endogenous oxidative DNA damage in carcinogenesis: what can we learn from repair-deficient mice?Comet-FISH with strand-specific probes reveals transcription-coupled repair of 8-oxoGuanine in human cells.Cockayne syndrome B protects against methamphetamine-enhanced oxidative DNA damage in murine fetal brain and postnatal neurodevelopmental deficitsGenomic DNA of Nostoc commune (Cyanobacteria) becomes covalently modified during long-term (decades) desiccation but is protected from oxidative damage and degradationCockayne syndrome B protein antagonizes OGG1 in modulating CAG repeat length in vivo.Genetic factors of age-related macular degeneration.Mfd is required for rapid recovery of transcription following UV-induced DNA damage but not oxidative DNA damage in Escherichia coli.Poly(ADP-ribosyl)ation accelerates DNA repair in a pathway dependent on Cockayne syndrome B proteinCockayne syndrome group B protein is engaged in processing of DNA adducts of lipid peroxidation product trans-4-hydroxy-2-nonenalRECQ1 plays a distinct role in cellular response to oxidative DNA damage.Human Cockayne syndrome B protein reciprocally communicates with mitochondrial proteins and promotes transcriptional elongation.Repair of mitochondrial DNA in aging and carcinogenesis.'To repair or not to repair - no longer a question': repair of mitochondrial DNA shielding against age and cancer.The CSB chromatin remodeler and CTCF architectural protein cooperate in response to oxidative stress.A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer.The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging.Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stressHuman embryonic stem cells have enhanced repair of multiple forms of DNA damage.Multiple interaction partners for Cockayne syndrome proteins: implications for genome and transcriptome maintenanceA ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repairAccumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice.Nucleic acid binding activity of human Cockayne syndrome B protein and identification of Ca(2+) as a novel metal cofactorComplete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome.Cockayne Syndrome group B protein stimulates NEIL2 DNA glycosylase activity.
P2860
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P2860
The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
The Cockayne Syndrome group B ...... ir of 8-hydroxyguanine in DNA.
@en
type
label
The Cockayne Syndrome group B ...... ir of 8-hydroxyguanine in DNA.
@en
prefLabel
The Cockayne Syndrome group B ...... ir of 8-hydroxyguanine in DNA.
@en
P2093
P356
P1476
The Cockayne Syndrome group B ...... air of 8-hydroxyguanine in DNA
@en
P2093
Brosh RM Jr
Dizdaroglu M
Rodriguez H
P304
45772-45779
P356
10.1074/JBC.M107888200
P407
P577
2001-10-01T00:00:00Z