The adaptive imbalance in base excision-repair enzymes generates microsatellite instability in chronic inflammation.
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Variant base excision repair proteins: contributors to genomic instabilityMicrosatellite instability in colorectal cancerHuman AP endonuclease suppresses DNA mismatch repair activity leading to microsatellite instability.Gut Microbiota Imbalance and Base Excision Repair Dynamics in Colon CancerTumor-specific microsatellite instability: do distinct mechanisms underlie the MSI-L and EMAST phenotypes?Transcriptional regulation of human DNA repair genes following genotoxic stress: trigger mechanisms, inducible responses and genotoxic adaptationStructural Basis for the Inhibition of Human Alkyladenine DNA Glycosylase (AAG) by 3,N4-Ethenocytosine-containing DNADifferential effects of reactive nitrogen species on DNA base excision repair initiated by the alkyladenine DNA glycosylaseEffect of Inulin on Proteome Changes Induced by Pathogenic Lipopolysaccharide in Human ColonRegulation of Rac1 and Reactive Oxygen Species Production in Response to Infection of Gastrointestinal EpitheliaGastrointestinal hyperplasia with altered expression of DNA polymerase beta.Bioenergetic metabolites regulate base excision repair-dependent cell death in response to DNA damage.Inflammation and oncogenesis: a vicious connection.The Mutyh base excision repair gene influences the inflammatory response in a mouse model of ulcerative colitis.Frameshift mutagenesis and microsatellite instability induced by human alkyladenine DNA glycosylase.Human base excision repair creates a bias toward -1 frameshift mutationsBoth base excision repair and O6-methylguanine-DNA methyltransferase protect against methylation-induced colon carcinogenesisMacrophages, nitric oxide and microRNAs are associated with DNA damage response pathway and senescence in inflammatory bowel diseaseThe p53 tumor suppressor network is a key responder to microenvironmental components of chronic inflammatory stress.Aag-initiated base excision repair promotes ischemia reperfusion injury in liver, brain, and kidney.Inflammatory colonic carcinogenesis: a review on pathogenesis and immunosurveillance mechanisms in ulcerative colitisSubstitution of active site tyrosines with tryptophan alters the free energy for nucleotide flipping by human alkyladenine DNA glycosylase.Interplay between DNA repair and inflammation, and the link to cancerEnzymatic MPG DNA repair assays for two different oxidative DNA lesions reveal associations with increased lung cancer riskChemistry meets biology in colitis-associated carcinogenesisNaturally occurring polyphenol, morin hydrate, inhibits enzymatic activity of N-methylpurine DNA glycosylase, a DNA repair enzyme with various roles in human disease.Infection, inflammation, and gastrointestinal cancer.Tumbling down a different pathway to genetic instability.Apurinic/Apyrimidinic endonuclease 1 regulates inflammatory response in macrophages.Ubiquitin ligase UBR3 regulates cellular levels of the essential DNA repair protein APE1 and is required for genome stabilityFractionated Radiation Exposure of Rat Spinal Cords Leads to Latent Neuro-Inflammation in Brain, Cognitive Deficits, and Alterations in Apurinic Endonuclease 1.Beyond translesion synthesis: polymerase κ fidelity as a potential determinant of microsatellite stability.Base excision repair: contribution to tumorigenesis and target in anticancer treatment paradigmsDNA repair is indispensable for survival after acute inflammation.Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancerAccumulation of oxidatively generated DNA damage in the brain: a mechanism of neurotoxicity.N-methylpurine DNA glycosylase inhibits p53-mediated cell cycle arrest and coordinates with p53 to determine sensitivity to alkylating agents.Targeting chemokine pathways in esophageal adenocarcinoma.Mechanisms of glycosylase induced genomic instabilityN-methylpurine DNA glycosylase and OGG1 DNA repair activities: opposite associations with lung cancer risk.
P2860
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P2860
The adaptive imbalance in base excision-repair enzymes generates microsatellite instability in chronic inflammation.
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
The adaptive imbalance in base ...... ility in chronic inflammation.
@ast
The adaptive imbalance in base ...... ility in chronic inflammation.
@en
The adaptive imbalance in base ...... ility in chronic inflammation.
@nl
type
label
The adaptive imbalance in base ...... ility in chronic inflammation.
@ast
The adaptive imbalance in base ...... ility in chronic inflammation.
@en
The adaptive imbalance in base ...... ility in chronic inflammation.
@nl
prefLabel
The adaptive imbalance in base ...... ility in chronic inflammation.
@ast
The adaptive imbalance in base ...... ility in chronic inflammation.
@en
The adaptive imbalance in base ...... ility in chronic inflammation.
@nl
P2093
P2860
P1476
The adaptive imbalance in base ...... bility in chronic inflammation
@en
P2093
Curtis C Harris
Irit Zurer
Leah E Mechanic
Leona D Samson
Lorne J Hofseth
Maria Kartalou
Meng Xu-Welliver
Mohammed A Khan
Olga Nikolayeva
Richard B Roth
P2860
P304
P356
10.1172/JCI19757
10.1172/JCI200319757
P407
P577
2003-12-01T00:00:00Z